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Being members of the same group and sharing DNA homology to a larger extent, they do create problems when their specific detection\u002Fidentification is attempted from different food and environmental sources. Numerous individual polymerase chain reaction (PCR) and few multiplex PCR (mPCR) methods have been employed to detect these organisms by targeting toxin genes but with lack of internal amplification control (IAC). Therefore, we attempted a mPCR with IAC for the detection of enterotoxic B. cereus group strains by selecting hbl A, nhe A and cyt K genes from B. cereus, indicative of the diarrheal potential and cry I A and pag genes, the plasmid borne phenotypic markers specific to B. thuringiensis and B. anthracis strains, respectively. Multiplex PCR assay validation was performed by simultaneous comparison with the results of single-target PCR assays and correlated to the classical conventional and biochemical identification of the organisms. The mPCR was able to detect as low as 101–102 organisms per ml following overnight enrichment of spiked food samples (vegetable biriyani and milk) in buffered peptone water (BPW). The presence of these organisms could also be detected by mPCR in naturally contaminated samples of rice based dishes and milk. The high throughput and cost-effective mPCR method described could provide a powerful tool for simultaneous, rapid and reliable detection of enterotoxic B. cereus group organisms.",{"EN":160,"VI":161},"Multiplex PCR assay for the detection of enterotoxic Bacillus cereus group strains and its application in food matrices","Xét nghiệm multiplex PCR phát hiện các chủng nhóm Bacillus cereus sinh độc tố ruột và ứng dụng trong các nền thực phẩm",{"VOID":163},"Drobniewski FA (1993) Bacillus cereus and related species. Clin Microbiol Rev 6:324–338\nGranum PE and Lund T (1997) Bacillus cereus and its food poisoning toxins. FEMS Microbiol Lett 157:223–228\nKotiranta A, Lounatmaa K and Haapasalo M (2000). Epidemiology and pathogenesis of Bacillus cereus infections. Mcrobes Infect 2:189–194\nGuinebretiere MH, Broussolle V and Nguyen-The C (2002) Enterotoxigenic profiles of food-poisoning and food-borne Bacillus cereus strains. J Clin Mcrobiol 40:3053–3056\nMckillip JL (2000) Prevalence and expression of enterotoxins in Bacillus cereus and other Bacillus spp., a literature review. Antonie Van Leeuwenhoek Int J Gen Mol Microbiol 77: 93–399\nSchoeni JL and Wong ACL (2005) Bacillus cereus food poisoning and its toxins. J Food Prot 68:636–648\nBeecher DJ, Shoeni JL and Wong ACL (1995) Enterotoxin activity of hemolysin BL from Bacillus cereus. Infect Immun 63:4423–4428\nGranum PE, O’sullivan K and Lund T (1999) The sequence of the non-hemolytic enterotoxin operon from Bacillus cereus. FEMS Microbiol Lett 177:225–229\nHardy SP, Lund T and Granum PE (2001) Cyt K toxin of Bacillus cereus forms pores in planar lipid bilayers and is cytotoxic to intestinal epithelia. FEMS Mcrobiol Lett 197: 47–51\nLindback T, Fagerlund A, Rodland MS and Granum PE (2004) Characterization of the Bacillus cereus Nhe enterotoxin. Mcrobiol 150:3959–3967\nLund T, De Buyser ML and Granum PE (2000). A new cytotoxin from Bacillus cereus that may cause necrotic enteritis. Mol Microbiol 38:254–261\nHansen BM and Hendriksen NB (2001) Detection of 1. enterotoxicBacillus cereus and Bacillus thuringiensis strains by PCR analysis. Appl Environ Microbiol 67:185–189\nSchnepf E, Crickmore N, Van Rien J, Lereclus D, Baum J, Feitelson J, Zeigler DR and Dean DH (1998) Bacillus thruingiensis and its pesticidal crystal proteins. Microbiol Mol Biol Rev 62:775–806\nDamgaard PH, Larsen HD, Hansen BM, Bresciani J and Jørgensen K (1996) Enterotoxin-producing strains of Bacillus thuringiensis isolated from food. Lett Appl Mcrobiol 23:146–150\nHendriksen NB and Hansen BM (1998) Phylogenetic relations of Bacillus thuringiensis: implications for risks associated to its use as a microbiological pest control agent. IOBC Bull 21:5–8\nJackson SG, Goodbrand RB, Ahmed R and Kasatiya S (1995) Bacillus cereus and Bacillus thuringiensis isolated in a gastroenteritis outbreak investigation. Lett Appl Mcrobiol 21:103–105\nRivera AMG, Granum PE and Priest FG (2000) Common occurrence of enterotoxin genes and enterotoxicity in Bacillus thuringiensis. FEMS Mcrobiol Lett 190:151–155\nMock M and Fouet A (2001) Anthrax. Ann Rev Mcrobiol 55:647–71\nHoffmaster AR, Hill KK, Gee JE, Marston CK, Popovic T, Sue D, Wilkins PP, Avashia SB, Drumgoole R, Helma CH, Ticknor LO, Okinaka RT and Jackson PJ (2006) Characterization of Bacillus cereus isolates associated with fatal pneumonias: strains are closely related to Bacillus anthracis and harbor B. anthracis virulence genes. J Clin Mcrobiol 44:3352–3360\nRasko DA, Ravel J, Okstad OA, et al. (2004) The genome sequence of Bacillus cereus ATCC 10987 reveals metabolic adaptations and a large plasmid related to Bacillus anthracis pXO1. Nucleic Acids Res 32:977–988\nKumar S, Balakrishna K and Batra HV (2006) Detection of Salmonella enterica serovar Typhi (S. typhi) by selective amplification of invA, viaB, ftiC-d and prt genes by polymerase chain reaction in multipex format. Lett Appl Mcrobiol 42:149–154\nTheron J, Morar D, du Preez M, Brözel VS and Venter SN (2001) A sensitive seminested PCR method for the detection of Shigella in spiked environmental water samples. Wat Res 35:869–874\nAndersen BGI, Skeie M, Sorhaug T, Langsrud T and Granum PE (2001) Growth and toxin profiles of Bacillus cereus isolated from different food sources. Int J Food Mcrobiol 69:237–246\nPark Hong S, Hyun Joong Kim, Jae Hwan Kim, Tae Woon Kim and Hae-Yeong Kim (2007) Simultaneous detection and identification of Bacillus cereus group bacteria using-multiplex PCR. J Mcrobiol Biotechnol 17(7):1177–1182\nPuriya N, Wasin B, Panuwat P, Chaiwat P, Mchio O, Apinya A and Watanalai P (2008) Broad distribution of enterotoxin genes (hblCDA, nheABC, cytK, and entFM) among Bacillus thuringiensis and Bacillus cereus as shown by novel primers. Int J Food Microbiol 121:352–356\nYang IC, Shih YCD, Huang T, Huang Y, Wang J and Tzu-Ming P (2005) Establishment of a novel multiplex PCR assay and detection of toxigenic strains of the species in the Bacillus cereus group. J Food Prot 68:2123–2130\nAbdel-Hameed A and Landén R (1994) Studies on Bacillus thuringiensis strains isolated from Swedish soils: insect toxicity and production of B. cereus-diarrhoeal-type enterotoxin. World J Mcrobiol Biotechnol 10:406–409\nHsieh YM, Sheu SJ, Chen YL and Tsen HY (1999) Enterotoxigenic profiles and polymerase chain reaction detection of Bacillus cereus group cells and B. cereus strains from foods and food-borne outbreaks. J Appl Mcrobiol 87:481–490\nCorona A, Fois MP, Mazzette R and De Santis EPL (2004) A New Multiplex PCR for the Detection of hbl Genes in Strains of the ’Bacillus cereus Group’. Vet Res Commun 27:679–682\nHoofar J, Cook N, Malorny B, Wagner M, De Medici D, Mawjood A and Fach P (2003) Making internal amplification control mandatory for diagnostic PCR. J Clin Mcrobiol 41:5835\nHenegariu O, Heerema N, Dlouhy SR, Vance G and Vogt PH (1997) Multiplex PCR: Critical parameters and step-by-step protocol. Bio Techniques 23:504–511",{"VOID":165},"10.1007\u002Fs12088-010-0002-4","PUBLICATION","VERIFIED","2025-02-18T15:25:21.482+00:00","Auto Verify",[171],"VI","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12088-010-0002-4",[174,190,204],{"id":175,"sortIndex":21,"researcher":20,"roles":176,"affiliations":178,"properties":187,"displayName":189,"givenName":20,"familyName":20},"627b8f23-fabe-45fa-8524-d5dd2aa98240",[177],"AUTHOR",[179],{"id":180,"sortIndex":21,"affiliation":181,"properties":20},"5f4fe625-f3b7-49a9-960c-bf8c37ad690c",{"id":180,"createTime":20,"updateTime":20,"relativeEntities":182,"slug":20,"properties":183,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":186,"statistic":20},[],{"title":184},{"VI":185},"Division of Microbiology, Defence Food Research Laboratory, Mysore, India",[],{"title":188},{"VI":189},"T. D. 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Despite enormous potential, its dependence on ultraviolet (UV) light for photocatalytic activity limits its commercialization. Accordingly in the present study, a photo catalytically superior ternary complex of TiO2 with Cadmium sulfide\u002FZinc sulfide (CdS\u002FZnS) has been synthesized, as well as, characterized for photo-induced antimicrobial activity. The band gap of crystalline TiO2\u002FCdS\u002FZnS nanocomposite has been reduced (2.26 eV) and nanocomposite has shown the optimal photo-activation at 590 nm. TiO2 nanocomposite has significant bactericidal activity in visible light (P \u003C 0.01). Exposure of the TiO2 nanocomposite affected the cellular metabolism by altering the 1681 metabolic features (P \u003C 0.001) culminating in poor cellular survivability. Additionally, photo-induced reactive oxygen species generation through nanocomposite disrupts the microbial cellular structure. The present study synthesized photocatalytic nanocomposite as well as unveiled the holistic cellular effect of theTiO2\u002FCdS\u002FZnS nanocomposite. Additionally, the present study also indicated the potential application of TiO2\u002FCdS\u002FZnS nanocomposite for sustainable environment management, therapeutics, and various industries.",{"EN":281},"Photocatalytic TiO2\u002FCdS\u002FZnS nanocomposite induces Bacillus subtilis cell death by disrupting its metabolism and membrane 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Nanomaterials (Basel) 10(2):387. https:\u002F\u002Fdoi.org\u002F10.3390\u002Fnano10020387","https:\u002F\u002Fdoi.org\u002F10.3390\u002Fnano10020387",{"mag":630,"pmc":631,"openalex":632,"pm":633,"doi":634},"3007214932","7075317","W3007214932","32102185","10.3390\u002Fnano10020387",{"id":636,"text":637,"url":638,"identifiers":639},"18171b9a-d6ba-439c-b6c3-a54042663680","Mittal A, Sharma S, Kumari V, Yadav S, Chauhan NS, Kumar N (2019) Highly efficient, visible active TiO2\u002FCdS\u002FZnS photocatalyst, study of activity in an ultra low energy consumption LED based photo reactor. J Mater Sci: Mater Electron 30:17933–17946. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10854-019-02147-6","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs10854-019-02147-6",{"doi":640},"10.1007\u002Fs10854-019-02147-6",{"id":20,"text":642,"url":643,"identifiers":644},"Ranjan S, Ramalingam C (2016) Titanium dioxide nanoparticles induce bacterial membrane rupture by reactive oxygen species generation. Environ Chem Lett 14:487–494. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10311-016-0586-y","https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10311-016-0586-y",{"mag":645,"openalex":646,"doi":647},"2521831054","W2521831054","10.1007\u002Fs10311-016-0586-y",{"id":20,"text":649,"url":650,"identifiers":651},"Planchon M, Léger T, Spalla O, Huber G, Ferrari R (2017) Metabolomic and proteomic investigations of impacts of titanium dioxide nanoparticles on Escherichia coli. PLoS ONE 12(6):e0178437. https:\u002F\u002Fdoi.org\u002F10.1371\u002Fjournal.pone.0178437","https:\u002F\u002Fdoi.org\u002F10.1371\u002Fjournal.pone.0178437",{"mag":652,"pmc":653,"openalex":654,"pm":655,"doi":656},"2621261669","5453534","W2621261669","28570583","10.1371\u002Fjournal.pone.0178437",{"id":20,"text":658,"url":659,"identifiers":660},"Dong Y, Zhu H, Shen Y, Zhang W, Zhang L (2019) Antibacterial activity of silver nanoparticles of different particle size against Vibrio natriegens. 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Nanoscale 8:6728–6738. https:\u002F\u002Fdoi.org\u002F10.1039\u002FC6NR00346J","http:\u002F\u002Fdx.doi.org\u002F10.1039\u002Fc6nr00346j",{"doi":675},"10.1039\u002Fc6nr00346j",{"id":20,"text":677,"url":678,"identifiers":679},"Patel SKS, Choi SH, Kang YC, Lee J-K (2017) Eco-friendly composite of Fe3O4-reduced graphene oxide particles for efficient enzyme immobilization. ACS Appl Mater Interfaces 9:2213–2222. https:\u002F\u002Fdoi.org\u002F10.1021\u002Facsami.6b05165","http:\u002F\u002Fdx.doi.org\u002F10.1021\u002Facsami.6b05165.s001",{"doi":680},"10.1021\u002Facsami.6b05165.s001",{"id":20,"text":682,"url":683,"identifiers":684},"Patel SKS, Anwar MZ, Kumar A, Otari SV, Pagolu R, Kim SY, Kim IW, Lee J-K (2018) Fe2O3 yolk-shell particles-based laccase biosensor for efficient detection of 2,6-dimethoxyphenol. Biochem Eng J 132:1–8. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.bej.2017.12.013","http:\u002F\u002Fdx.doi.org\u002F10.1016\u002Fj.bej.2017.12.013",{"doi":685},"10.1016\u002Fj.bej.2017.12.013",{"id":687,"text":688,"url":689,"identifiers":690},"4db02f93-b5f9-40e0-836c-fab310f70e24","Otari SV, Patel SKS, Kim S-Y, Haw JR, Kalia VC, Kim I-W, Lee J-K (2019) Copper ferrite magnetic nanoparticles for the immobilization of enzyme. Indian J Microbiol 59:105–108. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs12088-018-0768-3","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12088-018-0768-3",{"doi":691},"10.1007\u002Fs12088-018-0768-3",{"id":20,"text":693,"url":694,"identifiers":695},"Otari SV, Shinde VV, Gao H, Patel SKS, Kalia VC, Kim IW, Lee JK (2019) Biomolecule entrapped SiO2 nanoparticles for ultrafast green synthesis of silver nanoparticle-decorated hybrid nanostructures as effective catalyst. Ceram Int 45:5876–5882. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ceramint.2018.12.054","https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ceramint.2018.12.054",{"mag":696,"openalex":697,"doi":698},"2903703599","W2903703599","10.1016\u002Fj.ceramint.2018.12.054",{"id":20,"text":700,"url":701,"identifiers":702},"Patel SKS, Jeon MS, Gupta RK, Jeon Y, Kalia VC, Kim SC, Cho BK, Kim DR, Lee J-K (2019) Hierarchical macro-porous particles for efficient whole-cell immobilization: application in bioconversion of greenhouse gases to methanol. ACS Appl Mater Interfaces 11:18968–18977. https:\u002F\u002Fdoi.org\u002F10.1021\u002Facsami.9b03420","http:\u002F\u002Fdx.doi.org\u002F10.1021\u002Facsami.9b03420.s001",{"doi":703},"10.1021\u002Facsami.9b03420.s001",{"id":705,"text":706,"url":707,"identifiers":708},"f755baef-4be2-4d71-98c2-395a98c6961c","Kumar A, Park GD, Patel SKS, Kondaveeti S, Otari S, Anwar MZ, Kalia VC, Singh Y, Kim SC, Cho B-K, Sohn J-H, Kim DR, Kang YC, Lee J-K (2019) SiO2 microparticles with carbon nanotube-derived mesopores as an efficient support for enzyme immobilization. Chem Eng J 359:1252–1264. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.cej.2018.11.052","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS1385894718322861",{"doi":709},"10.1016\u002Fj.cej.2018.11.052",{"id":20,"text":711,"url":712,"identifiers":713},"Otari SV, Patel SKS, Kalia VC, Lee J-K (2020) One-step hydrothermal synthesis of magnetic rice straw for effective lipase immobilization and its application in esterification reaction. Bioresour Technol 302:122887. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.biortech.2020.122887","https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.biortech.2020.122887",{"mag":714,"openalex":715,"pm":716,"doi":717},"3001442170","W3001442170","32018086","10.1016\u002Fj.biortech.2020.122887",{"id":20,"text":719,"url":720,"identifiers":721},"Wu K, Wu P, Zhu J, Liu C, Dong X, Wu J, Meng G, Xu K, Hou J, Liu Z, Guo X (2019) Synthesis of hollow core-shell CdS@TiO2\u002FNi2P photocatalyst for enhancing hydrogen evolution and degradation of MB. Chem Eng J 360:221–230. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.cej.2018.11.211","https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.cej.2018.11.211",{"mag":722,"openalex":723,"doi":724},"2902571738","W2902571738","10.1016\u002Fj.cej.2018.11.211",{"id":20,"text":726,"url":727,"identifiers":728},"Azizi-Lalabadi M, Ehsani A, Divband B, Alizadeh-Sani M (2010) Antimicrobial activity of Titanium dioxide and Zinc oxide nanoparticles supported in 4A zeolite and evaluation the morphological characteristic. Sci Rep 9:17439. https:\u002F\u002Fdoi.org\u002F10.1038\u002Fs41598-019-54025-0","https:\u002F\u002Fdoi.org\u002F10.1038\u002Fs41598-019-54025-0",{"mag":729,"pmc":730,"openalex":731,"pm":732,"doi":733},"2990818650","6877518","W2990818650","31767932","10.1038\u002Fs41598-019-54025-0",{"id":20,"text":735,"url":736,"identifiers":737},"Ahmed V, Verma MK, Gupta S, Mandhan V, Chauhan NS (2018) Metagenomic profiling of soil microbes to mine salt stress tolerance genes. Front Microbiol 9:159. https:\u002F\u002Fdoi.org\u002F10.3389\u002Ffmicb.2018.00159","https:\u002F\u002Fdoi.org\u002F10.3389\u002Ffmicb.2018.00159",{"mag":738,"pmc":739,"openalex":740,"pm":741,"doi":742},"2789630303","5809485","W2789630303","29472909","10.3389\u002Ffmicb.2018.00159",{"id":20,"text":744,"url":745,"identifiers":746},"Hong Y, Zeng J, Wang X, Drlica K, Zhao X (2019) Post-stress bacterial cell death mediated by reactive oxygen species. Proc Natl Acad Sci USA 116:10064–10071. https:\u002F\u002Fdoi.org\u002F10.1073\u002Fpnas.1901730116","https:\u002F\u002Fdoi.org\u002F10.1073\u002Fpnas.1901730116",{"mag":747,"pmc":748,"openalex":749,"pm":750,"doi":751},"2927944686","6525477","W2927944686","30948634","10.1073\u002Fpnas.1901730116",{"id":20,"text":753,"url":754,"identifiers":755},"Rice KC, Bayles KW (2008) Molecular control of bacterial death and lysis. Microbiol Mol Biol Rev 72(1):85–109. https:\u002F\u002Fdoi.org\u002F10.1128\u002FMMBR.00030-07","https:\u002F\u002Fdoi.org\u002F10.1128\u002Fmmbr.00030-07",{"mag":756,"pmc":757,"openalex":758,"pm":759,"doi":760},"2128139766","2268280","W2128139766","18322035","10.1128\u002Fmmbr.00030-07",{"id":762,"createTime":763,"updateTime":764,"relativeEntities":765,"slug":766,"properties":767,"entityType":166,"verifyStatus":167,"verifyTime":778,"verifyNote":169,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":779,"fullTextUrl":20,"authors":780,"publicationType":218,"publisherRelationship":824,"citationCount":20,"citationInfo":20,"publishDate":870,"publishYear":871,"citationAnalyzeStatus":872,"lastCitationAnalyze":873,"indexDatabases":874,"openAccess":20,"references":20,"isForceReanalyzing":270},"adbcd188-f9f5-46c4-8172-cc52fbe98798","2024-01-04T14:31:20.875+00:00","2026-08-16T07:35:31.340+00:00",[],"Invitro-and-Invivo-Analysis-of-Human-Milk-Lactic-Acid-Bacteria-Isolates-for-Their-Anti-hypercholesterolemia-Actions",{"abstract":768,"title":770,"gsPaper":772,"references":774,"doi":776},{"EN":769},"The aim of this study was to evaluate the cholesterol lowering ability of Lactic Acid Bacteria (LAB) isolated from human breast milk under in vitro and in vivo conditions. Six LAB isolates namely Lacticaseibacillus casei 1A, Lactobacillus gasseri 5A, Enterococcus faecium 2C, Limosilactobacillus fermentum 3D, Pediococcus acidilactici 1C, and Lactiplantibacillus plantarum 7A, were examined for their bile resistance, bile salt hydrolase activity, cholesterol assimilation and viability in cholesterol rich; DeMan Rogosa and Sharpe broth, simulated gastric, small and upper intestinal conditions. During in vivo experiments, two putative LAB isolates were orally gavage to BALB\u002Fc mice, fed with normal basal and cholesterol rich (HCD) diets, daily for a period of 4 weeks. Blood serum analysis including total serum cholesterol, triglycerides, high-density and low-density lipoprotein (LDL) cholesterol levels and total fecal LAB counts of the animals were determined. The isolates in study showed bile resistance and bile salt hydrolysis activity, while significant differences (P \u003C 0.05) were seen in their cholesterol assimilation ability. L. gasseri 5A (195.67%) and L. plantarum 7A (193.78%) displayed highest cholesterol removal percentages, respectively. Animals in HCD, fed with L. gasseri 5A and L. plantarum 7A showed decreased levels of total cholesterol and LDL, compared to the control groups. In HCD group liver weight was increased, while fecal LAB counts were decreased. No changes were observed in behavior or body weight in all experimental groups. In conclusion, L. gasseri 5A and L. plantarum 7A isolated from human breast milk demonstrates significant hypocholesterolaemic actions in vitro and in vivo and might be considered a promising candidates for preventing hypercholesterolemia in man and animals.",{"EN":771},"Invitro and Invivo Analysis of Human Milk Lactic Acid Bacteria Isolates for Their Anti-hypercholesterolemia Actions",{"VOID":773},"[]",{"VOID":775},"Jung E, Kong SY, Ro YS et al (2022) Serum cholesterol levels and risk of cardiovascular death: a systematic review and a dose-response meta-analysis of prospective cohort studies. Int J Environ Res Public Health 19:8272. https:\u002F\u002Fdoi.org\u002F10.3390\u002Fijerph19148272\nVaduganathan M, Mensah G, Turco J et al (2022) The global burden of cardiovascular diseases and risk. 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Food Sci Nutr 8:6164–6173. https:\u002F\u002Fdoi.org\u002F10.1002\u002Ffsn3.1909",{"VOID":777},"10.1007\u002Fs12088-023-01150-0","2024-09-04T20:16:03.843+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12088-023-01150-0",[781,796,809],{"id":782,"sortIndex":21,"researcher":20,"roles":783,"affiliations":784,"properties":793,"displayName":795,"givenName":20,"familyName":20},"12a5af07-6d19-4dd7-a163-5d9ac677b31a",[177],[785],{"id":786,"sortIndex":21,"affiliation":787,"properties":20},"887d1095-a236-4ab8-b4e9-2f1bd778bf9b",{"id":786,"createTime":20,"updateTime":20,"relativeEntities":788,"slug":20,"properties":789,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":792,"statistic":20},[],{"title":790},{"VI":791},"Razi Vaccine and Serum Research Institute (RVSRI), Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran",[],{"title":794},{"VI":795},"Naheed Mojgani",{"id":797,"sortIndex":192,"researcher":20,"roles":798,"affiliations":799,"properties":806,"displayName":808,"givenName":20,"familyName":20},"a6c241bd-a73d-429c-9bfa-9676c5dc5e9c",[177],[800],{"id":786,"sortIndex":21,"affiliation":801,"properties":20},{"id":786,"createTime":20,"updateTime":20,"relativeEntities":802,"slug":20,"properties":803,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":805,"statistic":20},[],{"title":804},{"VI":791},[],{"title":807},{"VI":808},"Masoumeh Bagheri",{"id":810,"sortIndex":206,"researcher":20,"roles":811,"affiliations":812,"properties":821,"displayName":823,"givenName":20,"familyName":20},"4ad14566-8f07-4cab-a448-9002d93a4883",[177],[813],{"id":814,"sortIndex":21,"affiliation":815,"properties":20},"cdeec7b1-bc40-43cd-ba90-a6ac767e2771",{"id":814,"createTime":20,"updateTime":20,"relativeEntities":816,"slug":20,"properties":817,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":820,"statistic":20},[],{"title":818},{"EN":819},"Animal Science Research Institute of Iran (ASRI), Agriculture Research, Education and Extension Organization (AREEO), Karaj, Iran",[],{"title":822},{"VI":823},"Narges 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are a set of moral principles and values a civilized society follows. Doing science with principles of ethics is the bedrock of scientific activity. The society trusts that the results and the projected outcome of any scientific activity is based on an honest and conscientious attempt by the scientific community. However, during the last few decades, there has been an explosion of knowledge and the advent of digital age. We can access the publications of competitors with just a “click”. The evaluation parameters have evolved a lot and are based on impact factors, h-index and citations. There is a general feeling that the scientific community is under a lot of pressure for fulfilling the criteria for upward growth and even retention of the positions held. The noble profession of scientific research and academics has been marred by the temptation to falsify and fabricate data, plagiarism and other unethical practices. Broadly speaking, the breach of ethics involves: plagiarism, falsification of data, redundant (duplicate) publication, drawing far-fetched conclusions without hard data, for early publicity, gift authorship (receiving as well as giving), not giving sufficient attention and consideration to scholars and post-docs as per the norms, self promotion at the cost of team-members, treating colleagues (overall all juniors) in a feudal way and Machiavellianism (cunningness and duplicity in general conduct and push to positions of power and pelf). Misconduct in Indian academics and science is also under a lot of focus. It is important and urgent that science, engineering, and health departments and institutions in our country have in place systems for education and training in pursuit of science with ethics by sound and professional courses in Responsible Conduct of Research. All research and academic institution must have the Office of Ethics for information, guidelines, training and professional oversight of conduct of research with the ethos and ethics of research.",{"EN":885},"Ethics in Science",{"VOID":887},"[\"7882540606223534605\"]",{"VOID":889},"Resnik DB (2011) What is ethics in research and why is it important? http:\u002F\u002Fwww.niehs.nih.gov\u002Fresearch\u002Fresources\u002Fbioethics\u002Fwhatis\u002F\nOn being a scientist. A guide to responsible conduct in research. Third Edition (2009) graduateschool.nd.edu\u002Fassets\u002F21763\u002Fon_being_a_scientist.pdf\nSteneck NH (2007) Office of research integrity—introduction to responsible conduct of research. Department of Health and Human Services, USA. http:\u002F\u002Fori.hhs.gov\u002Fori-intro\nSumner JB (1946) The chemical nature of enzymes. Nobel Prize Lecture. http:\u002F\u002Fwww.nobelprize.org\u002Fnobel_prizes\u002Fchemistry\u002Flaureates\u002F1946\u002Fsumner-lecture.html\nChemistry explained. James Sumner, American Biochemist. http:\u002F\u002Fwww.chemistryexplained.com\u002FSt-Te\u002FSumner-James.html\nWatson JD (2001) The double helix: a personal account of the discovery of the structure of DNA. Simon and Schuster, New York\nSharma OP (2012) Quality indicators of scientific research. Indian J Microbiol 52:305–306. doi:10.1007\u002Fs12088-012-0246-2\nPendlebury DA (2008) White paper—using bibliometrics in evaluating research. wokinfo.com\u002Fmedia\u002Fmtrp\u002FUsingBibliometricsinEval_WP.pdf\nPublish and perish at Imperial College London: the death of Stefan Grimm (2014) http:\u002F\u002Fwww.dcscience.net\u002F2014\u002F12\u002F01\u002Fpublish-and-perish-at-imperial-college-london-the-death-of-stefan-grimm\u002F\nAl-Khalili J (2010) Higgs would not find his boson in today’s ‘publish or perish’ research culture. http:\u002F\u002Fwww.theguardian.com\u002Fcommentisfree\u002F2014\u002Ffeb\u002F14\u002Fhiggs-boson-publish-or-perish-science-culture\nZimmer C (2012) A sharp rise in retractions prompts calls for reform. http:\u002F\u002Fwww.nytimes.com\u002F2012\u002F04\u002F17\u002Fscience\u002Frise-in-scientific-journal-retractions-prompts-calls-for-reform.html?pagewanted=all&_r=0\nFang FC, Casadevall A, Morrison RP (2011) Retracted science and the retraction index. Infect Immun 79:3855–3859. doi:10.1128\u002FIAI.05661-11\nWalker L (2014) Is pressure to publish causing scientific fraud? http:\u002F\u002Fthebrainbank.scienceblog.com\u002F2014\u002F04\u002F11\u002Fis-pressure-to-publish-causing-scientific-fraud\u002F\nCounzin-Frankel J (2013) Shaking up science. Science 339:386–389. doi:10.1126\u002Fscience.339.6118.386\nMaher B (2010) Research integrity: Sabotage! Nature 467:516–518. doi:10.1038\u002F467516a\nCommittee on Publication Ethics. http:\u002F\u002Fpublicationethics.org\u002F\nAlbert T, Wager E (2003) How to handle authorship disputes: a guide for new researchers. COPE report 2003. publicationethics.org\u002Ffiles\u002F2003pdf12.pdf\nAlberts B (2010) Promoting scientific standards. Science 327:12. doi:10.1126\u002Fscience.1185983\nEditorial—Mentoring matters (2010) Nature Cell Biol 12:101. doi:10.1038\u002Fncb0210-101\nLee A, Dennis C, Campbell P (2007) Nature’s guide for mentors. Nature 447:791–797. doi:10.1038\u002F447791a\nTitus SL, Wells JA, Rhoades LJ (2008) Repairing research integrity. Nature 453:980–982. doi:10.1038\u002F453980a\nKelland K (2012) UK survey finds science misconduct “alive and well”. http:\u002F\u002Fwww.reuters.com\u002Farticle\u002F2012\u002F01\u002F12\u002Fus-scientists-research-survey-idUSTRE80B1DN20120112\nWoodgett J (2012) We must be open about our mistakes. Nature 489:7. doi:10.1038\u002F489007a\nSingapore statement on research integrity (2010) http:\u002F\u002Fwww.singaporestatement.org\u002F\nFanelli D (2013) Redefine misconduct as distorted reporting. Nature 494:149. doi:10.1038\u002F494149a\nChallenges in irreproducible research (2014) Nature 515:7. doi:10.1038\u002F515007a\nAnnouncement: reducing our irreproducibility (2013) Nature 496:398. doi:10.1038\u002F496398a\nResponsible Conduct of Research (RCR) http:\u002F\u002Fwww.nsf.gov\u002Fbfa\u002Fdias\u002Fpolicy\u002Frcr.jsp\nInnovation and growth—rationale for innovation strategy. Organization for Economic Co-operation and development (2007) www.oecd.org\u002Fscience\u002Finno\u002F39374789.pdf\nSatyanarayana K (2010) Plagiarism: a scourge afflicting the Indian science. Indian J Med Res 131:373–376\nChaddah P (2014) Pursuing knowledge creation, India needs a policy on ‘plagiarism cells’. Curr Sci 106:349\nAbinandanan TA (2011) Scientific misconduct in India: an analysis of retracted papers in PubMed. http:\u002F\u002Fwww.imsc.res.in\u002F~ethicsmeet\u002Fabstracts\u002Fabinandanan.html\nJayaraman K (2008) Chemistry’s ‘colossal’ fraud. http:\u002F\u002Fwww.rsc.org\u002Fchemistryworld\u002FNews\u002F2008\u002FMarch\u002F25030801.asp\nNeelankantan S (2009) In India, plagiarism on the rise. http:\u002F\u002Fwww.globalpost.com\u002Fdispatch\u002Findia\u002F090921\u002Fdid-you-write-yaar-india-plagiarism-the-rise\nIndia to propose regulatory body to curb misconduct. Nature News in Brief (2008) Nature 452:15\nTurnitin. http:\u002F\u002Fturnitin.com\u002F\nOffice of Research Ethics. https:\u002F\u002Fuwaterloo.ca\u002Fresearch\u002Foffice-research-ethics",{"VOID":891},"10.1007\u002Fs12088-015-0532-x","2024-05-13T13:51:32.511+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12088-015-0532-x",[895],{"id":896,"sortIndex":21,"researcher":20,"roles":897,"affiliations":898,"properties":907,"displayName":909,"givenName":20,"familyName":20},"3a154389-f2de-4ec5-8fc0-9c3474018344",[177],[899],{"id":900,"sortIndex":21,"affiliation":901,"properties":20},"d6de9557-b11d-443e-8808-2e6777de0353",{"id":900,"createTime":20,"updateTime":20,"relativeEntities":902,"slug":20,"properties":903,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":906,"statistic":20},[],{"title":904},{"VI":905},"Institute of Himalayan Bioresource Technology (CSIR), Palampur, India",[],{"title":908,"gsAuthor":910},{"VI":909},"Om P. 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To evaluate the influence of the storage condition on the composition of cell fatty acids, genetic profile and biochemical characteristics of Xanthomonas campestris pv. mangiferaeindicae IBSBF 2103, as well as, to identify its relationship with the yielding and viscosity of the xanthan gum produced, this study monitored the strain preserved in two simple and widely used conditions, ultra-freezer (−80 °C) and refrigeration (3–8 °C) during 5 months. Were identified and quantified 13 fatty acids. The cells preserved at −80 °C showed more stable concentration of all fatty acids, producing more xanthan gum and with higher viscosity. The chromosomal analysis obtained with the enzyme XbaI revealed 17 distinct fragments with maximum size of 485 kilobases, without variations among the subcultures maintained in both storage conditions. 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Res Microbiol 164:466–479. doi:10.1016\u002Fj.resmic.2013.02.005","https:\u002F\u002Fwww.sciencedirect.com\u002Fscience\u002Farticle\u002Fpii\u002FS0923250813000260",{"doi":1302},"10.1016\u002Fj.resmic.2013.02.005",{"id":20,"text":1304,"url":20,"identifiers":1305},"Brandão LV, Assis DJ, Lopez JA, Esperidião MCA (2013) Bioconversion of crude glycerin derived from biodiesel to xanthan gum. Braz J Chem Eng 30:737–746. doi:10.1590\u002FS0104-66322013000400006",{"doi":1306},"10.1590\u002FS0104-66322013000400006",{"id":20,"text":1308,"url":1309,"identifiers":1310},"Brandão LV, Esperidião MCA, Druzian JI (2010) Utilização do soro de mandioca como substrato fermentativo para a biossíntese de goma xantana: viscosidade aparente e produção. Polímeros 20:175–180. doi:10.1590\u002FS0104-14282010005000029","https:\u002F\u002Fdoi.org\u002F10.1590\u002Fs0104-14282010005000029",{"doi":1311},"10.1590\u002Fs0104-14282010005000029",{"id":1313,"createTime":1314,"updateTime":1315,"relativeEntities":1316,"slug":1317,"properties":1318,"entityType":166,"verifyStatus":167,"verifyTime":1331,"verifyNote":169,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":1332,"fullTextUrl":20,"authors":1333,"publicationType":218,"publisherRelationship":1456,"citationCount":1499,"citationInfo":1500,"publishDate":1502,"publishYear":1133,"citationAnalyzeStatus":1136,"lastCitationAnalyze":1315,"indexDatabases":1503,"openAccess":20,"references":20,"isForceReanalyzing":270},"74e0accb-94ce-4a4d-804d-63cc524815bf","2024-04-08T08:10:39.476+00:00","2026-07-20T01:47:18.458+00:00",[],"Mycobacterium-mageritense-Parotitis-in-an-Immunocompetent-Adult",{"abstract":1319,"title":1321,"gsPaper":1323,"keywords":1325,"references":1327,"doi":1329},{"EN":1320},"\n                Mycobacterium mageritense, a rapidly growing mycobacterium, is a rare clinical pathogen. Furthermore, parotitis due to non-tuberculosis mycobacterium is very rare in adults. Herein, we report the first case of M. mageritense parotitis in an immunocompetent adult. A 40-year-old man presented with swelling in a left parotid lesion. He was diagnosed with parotitis. The culture from the parotid abscess grew M. mageritense. He was unsuccessfully treated with levofloxacin monotherapy. Trimethoprim–sulfamethoxazole was added, leading to some clinical response; however, the erythema persisted despite 14 months of antibiotic therapy. Subsequently, the skin lesion was surgically removed. The antibiotic treatment was ceased a week after surgery as the postoperative course was uneventful and the lesion had improved. No recurrence was noted at 7 months after surgery. Although extremely rare, M. mageritense can cause parotitis in immunocompetent adults, and may not be sufficiently treated with antibiotics alone.",{"EN":1322},"Mycobacterium mageritense Parotitis in an Immunocompetent Adult",{"VOID":1324},"[\"3179983576426680866\"]",{"EN":1326},"",{"VOID":1328},"Domenech P, Jimenez MS, Menendez MC, Bull TJ, Samper S, Manrique A et al (1997) Mycobacterium mageritense sp. nov. Int J Syst Bacteriol 47:535–540. https:\u002F\u002Fdoi.org\u002F10.1099\u002F00207713-47-2-535\nWang Y, Ogawa M, Fukuda K, Miyamoto H, Taniguchi H (2006) Isolation and identification of mycobacteria from soils at an illegal dumping site and landfills in Japan. Microbiol Immunol 50:513–524. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1348-0421.2006.tb03821.x\nGira AK, Reisenauer AH, Hammock L, Nadiminti U, Macy JT, Reeves A et al (2004) Furunculosis due to Mycobacterium mageritense associated with footbaths at a nail salon. J Clin Microbiol 42:1813–1817. https:\u002F\u002Fdoi.org\u002F10.1128\u002FJCM.42.4.1813-1817.2004\nWallace RJ Jr, Brown-Elliott BA, Hall L, Roberts G, Wilson RW, Mann LB et al (2002) Clinical and laboratory features of Mycobacterium mageritense. J Clin Microbiol 40:2930–2935. https:\u002F\u002Fdoi.org\u002F10.1128\u002FJCM.40.8.2930-2935.2002\nAppelgren P, Farnebo F, Dotevall L, Studahl M, Jönsson B, Petrini B (2008) Late-onset posttraumatic skin and soft-tissue infections caused by rapid-growing mycobacteria in tsunami survivors. Clin Infect Dis 47:e11–e16. https:\u002F\u002Fdoi.org\u002F10.1086\u002F589300\nAli S, Khan FA, Fisher M (2007) Catheter-related bloodstream infection caused by Mycobacterium mageritense. J Clin Microbiol 45:273. https:\u002F\u002Fdoi.org\u002F10.1128\u002FJCM.01224-06\nFukunaga M, Goya M, Ogawa M, Fukuda K, Taniguchi H, Ando K et al (2016) Implantable cardioverter defibrillator infection due to Mycobacterium mageritense. J Infect Chemother 22:180–183. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.jiac.2015.09.010\nMcMullen AR, Mattar C, Kirmani N, Burnham CA (2015) Brown-pigmented Mycobacterium mageritense as a cause of prosthetic valve endocarditis and bloodstream infection. J Clin Microbiol 53:2777–2780. https:\u002F\u002Fdoi.org\u002F10.1128\u002FJCM.01041-15\nMuñoz-Sanz A, Rodríguez-Vidigal FF, Vera-Tomé A, Jiménez MS (2013) Mycobacterium mageritense meningitis in an immunocompetent patient with an intrathecal catheter. Enferm Infecc Microbiol Clin 31:59–60. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.eimc.2012.05.007\nGordon Huth R, Brown-Elliott BA, Wallace RJ Jr (2011) Mycobacterium mageritense pulmonary disease in patient with compromised immune system. Emerg Infect Dis 17:556–558. https:\u002F\u002Fdoi.org\u002F10.3201\u002Feid1703.101279\nWolinsky E (1995) Mycobacterial lymphadenitis in children: a prospective study of 105 nontuberculous cases with long-term follow-up. Clin Infect Dis 20:954–963. https:\u002F\u002Fdoi.org\u002F10.1093\u002Fclinids\u002F20.4.954\nYamanaka T, Okamoto H, Hosoi H (2013) Non-tuberculous mycobacterial infection of the parotid gland in an immunocompetent elderly patient. BMJ Case Rep. https:\u002F\u002Fdoi.org\u002F10.1136\u002Fbcr-2013-200990\nGriffith DE, Aksamit T, Brown-Elliott BA, Catanzaro A, Daley C, Gordin F et al (2007) ATS Mycobacterial Diseases Subcommittee; American Thoracic Society; Infectious Disease Society of America. An official ATS\u002FIDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med 175:367–416. https:\u002F\u002Fdoi.org\u002F10.1164\u002Frccm.200604-571ST\nZimmermann P, Tebruegge M, Curtis N, Ritz N (2015) The management of non-tuberculous cervicofacial lymphadenitis in children: a systematic review and meta-analysis. J Infect 71:9–18. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.jinf.2015.02.010",{"VOID":1330},"10.1007\u002Fs12088-017-0692-y","2024-04-30T10:01:52.360+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12088-017-0692-y",[1334,1349,1370,1385,1398,1413,1428,1443],{"id":1335,"sortIndex":21,"researcher":20,"roles":1336,"affiliations":1337,"properties":1346,"displayName":1348,"givenName":20,"familyName":20},"bc656d85-5979-447e-94ef-ff7d83ca3015",[177],[1338],{"id":1339,"sortIndex":21,"affiliation":1340,"properties":20},"539533cd-9b5c-437f-ab50-852fd84cff30",{"id":1339,"createTime":20,"updateTime":20,"relativeEntities":1341,"slug":20,"properties":1342,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1345,"statistic":20},[],{"title":1343},{"VI":1344},"Division of Infectious Diseases, Jichi Medical University Hospital, Shimotsuke, Japan",[],{"title":1347},{"VI":1348},"Taro Okabe",{"id":1350,"sortIndex":192,"researcher":20,"roles":1351,"affiliations":1352,"properties":1367,"displayName":1369,"givenName":20,"familyName":20},"978159e6-d1e4-4a74-918f-05288cf41dd6",[177],[1353,1361],{"id":1354,"sortIndex":21,"affiliation":1355,"properties":20},"89cb918a-af28-46d8-86b1-38ed42e026b7",{"id":1354,"createTime":20,"updateTime":20,"relativeEntities":1356,"slug":20,"properties":1357,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1360,"statistic":20},[],{"title":1358},{"VI":1359},"Department of Infection and Immunity, School of Medicine, Jichi Medical University, Shimotsuke, Japan",[],{"id":1339,"sortIndex":21,"affiliation":1362,"properties":20},{"id":1339,"createTime":20,"updateTime":20,"relativeEntities":1363,"slug":20,"properties":1364,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1366,"statistic":20},[],{"title":1365},{"VI":1344},[],{"title":1368},{"VI":1369},"Teppei 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Onishi",{"id":1399,"sortIndex":125,"researcher":20,"roles":1400,"affiliations":1401,"properties":1410,"displayName":1412,"givenName":20,"familyName":20},"b5b356bd-8a1a-421d-9591-5afb788b7caa",[177],[1402],{"id":1403,"sortIndex":21,"affiliation":1404,"properties":20},"29b89713-b96c-4180-b7f9-dfa93ff0253e",{"id":1403,"createTime":20,"updateTime":20,"relativeEntities":1405,"slug":20,"properties":1406,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1409,"statistic":20},[],{"title":1407},{"VI":1408},"Department of Internal Medicine, Saiseikai Utsunomiya Hospital, Utsunomiya, Japan",[],{"title":1411},{"VI":1412},"Masayoshi Komura",{"id":1414,"sortIndex":353,"researcher":20,"roles":1415,"affiliations":1416,"properties":1425,"displayName":1427,"givenName":20,"familyName":20},"77d300ad-560f-427e-b985-41317e36a394",[177],[1417],{"id":1418,"sortIndex":21,"affiliation":1419,"properties":20},"aabc8ec4-6e1b-4326-b292-f95c2859dd39",{"id":1418,"createTime":20,"updateTime":20,"relativeEntities":1420,"slug":20,"properties":1421,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1424,"statistic":20},[],{"title":1422},{"VI":1423},"Department of Clinical Laboratory, Saiseikai Utsunomiya Hospital, Utsunomiya, Japan",[],{"title":1426},{"VI":1427},"Shigehiro Hagiwara",{"id":1429,"sortIndex":369,"researcher":20,"roles":1430,"affiliations":1431,"properties":1440,"displayName":1442,"givenName":20,"familyName":20},"3ee0c794-286a-481c-ae9d-d585a8cf9d2c",[177],[1432],{"id":1433,"sortIndex":21,"affiliation":1434,"properties":20},"7269da00-0352-40a4-9a84-b1efd534a532",{"id":1433,"createTime":20,"updateTime":20,"relativeEntities":1435,"slug":20,"properties":1436,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1439,"statistic":20},[],{"title":1437},{"VI":1438},"Clinical Laboratory Center, Dokkyo Medical University Hospital, Mibu, Japan",[],{"title":1441},{"VI":1442},"Hiromichi Suzuki",{"id":1444,"sortIndex":95,"researcher":20,"roles":1445,"affiliations":1446,"properties":1453,"displayName":1455,"givenName":20,"familyName":20},"280d49e5-10c9-41e9-8f95-16b09b447073",[177],[1447],{"id":1339,"sortIndex":21,"affiliation":1448,"properties":20},{"id":1339,"createTime":20,"updateTime":20,"relativeEntities":1449,"slug":20,"properties":1450,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":1452,"statistic":20},[],{"title":1451},{"VI":1344},[],{"title":1454},{"VI":1455},"Yuji 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spp. is one of the main causative agents of dermatophytosis such as tinea ungium and tinea pedis. Resistance to antifungal drugs is a significant clinical problem in dermatophytosis. The main molecular mechanism of antifungal resistance to conventional therapy in dermatophytes is the expression of efflux pumps. Efforts aimed at improving the efficacy of current antifungals such as griseofulvin are relevant. Given this, sesquiterpenes such as α-bisabolol and nerolidol found in essential oils represent promissing alternatives. Griseofulvin sensitivity modulation activity in T. rubrum, T. interdigitale H6, and T. interdigitale Δmdr2 (mutant strain of T. interdigitale) promoted by α-bisabolol and nerolidol were investigated. The minimum inhibitory concentration (MIC) of the test drugs were determined by microdilution. Subsequently, the effect of the drugs tested on plasma membrane functionality (K+ release) was analyzed. The MIC of griseofulvin was determined at sub-inhibitory sesquiterpene concentrations (modulation assay). An association study was performed with griseofulvin and sesquiterpenes (checkerboard). α-bisabolol was more potent than nerolidol; presenting lower MIC values. All of the fungi were sensitive to griseofulvin, starting at 8 µg\u002FmL. With the exception of griseofulvin, all of the test drugs increased K+ release (p \u003C 0.05). Nerolidol modulated the sensitivity of all strains to griseofulvin; α-bisabolol sensitivity modulation was limited to T. interdigitale H6 and T. interdigitale Δmdr2. In association with griseofulvin: nerolidol and α-bisabolol respectively presented synergism and additivity. Finally, the results of our study suggest using α-bisabolol and nerolidol compounds as potential antifungal agents and griseofulvin sensitivity modulators for Trichophyton spp.",{"EN":1514},"The Sensitivity Modifying Activity of Nerolidol and α-Bisabolol Against Trichophyton spp",{"VOID":1516},"[\"15067127321116195921\"]",{"VOID":1518},"Ahmad A, Khan A, Manzoor N (2013) Reversal of efflux mediated antifungal resistance underlies synergistic activity of two monoterpenes with fluconazole. Eur J Pharm Sci 48:80–86. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ejps.2012.09.016\nBoral H, Metin B, Dogen A, Seyedmousavi S, Ilkit M (2018) Overview of selected virulence attributes in Aspergillus fumigatus, Candida albicans, Cryptococcus neoformans, Trichophyton rubrum, and Exophiala dermatitidis. Fungal Genet Biol 111:92–107. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.fgb.2017.10.008\nChan W, Tan LT, Chan K, Lee L, Goh B (2016) Nerolidol: a sesquiterpene alcohol with multi-faceted pharmacological and biological activities. Molecules. 21:529. https:\u002F\u002Fdoi.org\u002F10.3390\u002Fmolecules21050529\nClinical and Laboratory Standards Institute (2008) Reference method for broth dilution antifungal susceptibility testing of filamentous fungi. Approved standard—second edition M38-A2. Pennsylvania, United States of America\nCorrea-Royero J, Tangarife V, Durán C, Stashenko E, Mesa-Arango A (2010) In vitro antifungal activity and cytotoxic effect of essential oils and extracts of medicinal and aromatic plants against Candida krusei and Aspergillus fumigatus. Rev Bras Farmacogn 20:734–741. https:\u002F\u002Fdoi.org\u002F10.1590\u002FS0102-695X2010005000021\nCoutinho HD, Costa JGM, Lima EO, Silva VSF, Siqueira-Júnior JP (2008) Enhancement of the antibiotic activity against a multiresistant Escherichia coli by Mentha arvensis L. and chlorpromazine. Chemother 54:328–330. https:\u002F\u002Fdoi.org\u002F10.1159\u002F000151267\nLage TCA, Montanari RM, Fernandes AS, Monteiro CMO, Senra TOS, Zeringota V, Matos RS, Daemon E (2015) Chemical composition and acaricidal activity of the essential oil of Baccharis dracunculifolia de Candole (1836) and its constituents nerolidol and limonene on larvae and engorged females of Rhipicephalus microplus (Acari: Ixodidae). Exp Parasitol 148:24–29. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.exppara.2014.10.011\nFachin AL, Ferreira-Nozawa M, Maccheroni-Jr W, Martinez-Rossi N (2006) Role of the ABC transporter TruMDR2 in terbinafine, 4-nitroquinoline N-oxide and ethidium bromide susceptibility in Trichophyton rubrum. J Med Microbiol 55:1093–1099. https:\u002F\u002Fdoi.org\u002F10.1099\u002Fjmm.0.46522-0\nFajinmi OO, Kulkarni MG, Benická S, Zeljkovic SC, Dolezal K, Tarkowski P, Finnie JF, Staden JV (2018) Antifungal activity of the volatiles of Agathosma betulina and Coleonema album commercial essential oil and their effect on the morphology of fungal strains Trichophyton rubrum and T. mentagrophytes. South Afr J Bot 122:492–497. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.sajb.2018.03.003Get\nForrer M, Kulik EM, Filippi A, Waltimo T (2013) The antimicrobial activity of alpha-bisabolol and tea tree oil against Solobacterium moorei, a gram-positive bacterium associated With halitosis. Arch Oral Biol 58:10–16. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.archoralbio.2012.08.001\nFuentefria AM, Pippi B, Lana DFD, Donato KK, Andrade SF (2017) Antifungals: an insight into new strategies to combat antifungal resistance. Lett Appl Microbiol 66:2–13. https:\u002F\u002Fdoi.org\u002F10.1111\u002Flam.12820\nGalgóczy L, Bácsi A, Homa M, Virágh M, Papp T, Vágvölgyi C (2011) In vitro antifungal activity of phenothiazines and their combination with amphotericin B against different Candida species. Mycoses 54:737–743. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1439-0507.2010.02010.x\nGhelardi E, Celandroni F, Gueye SA, Salvetti S, Senesi S, Bulgheroni A, Mailland F (2014) Potential of Ergosterol synthesis inhibitors to cause resistance or cross-resistance in Trichophyton rubrum. Antimicrob Agents Chemother 58:2825–2829. https:\u002F\u002Fdoi.org\u002F10.1128\u002FAAC.02382-13\nKapp E, Malan SF, Joubert J, Sampson SL (2018) Small molecule efflux pump inhibitors in Mycobacterium tuberculosis: a rational drug design perspective. Mini Rev Med Chem 18:72–86. https:\u002F\u002Fdoi.org\u002F10.2174\u002F1389557517666170510105506\nLewis RE, Diekema DJ, Messer SA, Pfaller MA, Klepser ME (2002) Comparison of Etest, chequerboard dilution and time-kill studies for the detection of synergy or antagonism between antifungal agents tested against Candida species. J Antimicrob Chemother 49:345–351. https:\u002F\u002Fdoi.org\u002F10.1093\u002Fjac\u002F49.2.345\nLopes G, Pinto E, Salgueiro L (2017) Natural Products: an alternative to conventional therapy for dermatophytosis? Mycopathol 182:143–167. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11046-016-0081-9\nMartinez-Rossi NM, Bitencourt TA, Peres NTA, Lang EAS, Gomes EV, Quaresemin NR, Martins MP, Lopes L, Rossi A (2018) Dermatophyte resistance to antifungal drugs: mechanisms and prospectus. Front Microbiol 9:1108. https:\u002F\u002Fdoi.org\u002F10.3389\u002Ffmicb.2018.01108\nMeireles ALP, Costa MS, Rocha KAS, Gusevskaya EV (2015) Heteropoly acid catalyzed cyclization of nerolidol and farnesol: synthesis of α-bisabolol. Appl Catal A 502:271–275. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.apcata.2015.06.022\nPark MJ, Gwak KS, Yang I, Kim KW, Jeung EB, Chang JW, Choi IG (2009) Effect of citral, eugenol, nerolidol and α-terpineol on the ultrastructural changes of Trichophyton mentagrophytes. Fitoterapia 80:290–296. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.fitote.2009.03.007\nPule CM, Sampson SL, Warren RM, Black PA, van Helden PD, Victor TC, Louw GE (2015) Efflux pump inhibitors: targeting mycobacterial efflux systems to enhance TB therapy. J Antimicrob Chemother 71:17–26. https:\u002F\u002Fdoi.org\u002F10.1093\u002Fjac\u002Fdkv316\nRaut JS, Karuppayil SM (2014) A status review on the medicinal properties of essential oils. Ind Crops Prod 62:250–264. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.indcrop.2014.05.055\nReuk-ngam N, Chimnoi N, Khunnawutmanotham N, Techasakul S (2014) Antimicrobial activity of coronarin D and its synergistic potential with antibiotics. BioMed Res In 2014:1–8. https:\u002F\u002Fdoi.org\u002F10.1155\u002F2014\u002F581985\nRomagnoli C, Baldisserotto A, Malisardi G, Vicentini CB, Mares D, Andreotti E, Vertuani S, Manfredini S (2015) A multi-target approach toward the development of novel candidates for antidermatophytic activity: ultrastructural evidence on α-bisabolol-Treated Microsporum gypseum. Molecules 20:11765–11776. https:\u002F\u002Fdoi.org\u002F10.3390\u002Fmolecules200711765\nRottini MM, Amaral ACF, Ferreira JLP, Silva JRA, Taniwaki NN, Souza CSF, d’Escoffier LN, Almeida-Souza F, Hardoim DJ, Costa SCG, Calabrese KS (2015) In vitro evaluation of (–) α-bisabolol as a promising agent against Leishmania amazonensis. Exp Parasitol 148:66–72. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.exppara.2014.10.001\nSantos DA, Barros MES, Hamdan JS (2006) Establishing a method of inoculum preparation for susceptibility testing of Trichophyton rubrum and Trichophyton mentagrophytes. 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Tea from mangrove plant Ceriops decandra was administered against DMBA induced buccal pouch carcinoma in hamster rats. The chemical constitutions and quality of mangrove tea is similar with the commercial tea Camellia sinensis. The Hamster rats were painted thrice a week with DMBA in their right buccal pouch, and also administrated orally with 1.25% of Ceriops tea extract, on alternate days of the DMBA treatment. Appropriate control animals were maintained. After 14 weeks of treatment, bacterial species in saliva were enumerated, tumor incidences were analyzed using histopathological section and tumor volume in the animals was quantified using water-displaced method. The decreased counts of beneficial bacteria and increased counts of harmful bacteria were associated with increased volume of tumors. The present study concluded that the tea extract from C. decandra prevents the oral cancer incidences and maintain the good health conditions of the animals.",{"EN":2020},"Effect of Mangrove Tea Extract from Ceriops decandra (Griff.) Ding Hou. on Salivary Bacterial Flora of DMBA Induced Hamster Buccal Pouch Carcinoma",{"VOID":2022},"[\"3507223408378574375\"]",{"VOID":2024},"Sugerman PB, Joseph BK, Savage NW (1995) The role of oncogenes, tumor suppressor genes and growth factors in oral squamous cell carcinoma: a case of apoptosis versus proliferation. Oral Dis 1:172–188\nRodrigues VC, Moss SM, Tuomainen H (1998) Oral cancer in the UK: to screen or not to screen. Oral Oncol 34:454–465\nChen AY, Myers JN (2001) Cancer of the oral cavity. Dis Mon 47:274–361\nBrown AE, Langdon JD (1995) Management of oral cancer. Ann R Coll Surg Engl 77:404–408\nZakrzewska JM (1999) Fortnightly review: oral cancer. BMJ 318:1051–1054\nNagy KN, Sondoki I, Szoke I, Nagy E, Newman HN (1998) The microflora associated with human oral carcinomas. Oral Oncol 34:304–308\nMager DL, Haffajee AD, Devlin PM, Norris CM, Posner MR, Goodson JM (2005) The salivary microbiota as a diagnostic indicator of oral cancer: A descriptive, non-randomized study of cancer-free and oral squamous cell carcinoma subjects. J Transl Med 3:1–8\nFriedman M, Mackey BE, Kim HJ (2007) Structure-activity relationships of tea compounds against human cancer cells. J Agric Food Chem 55:243–253\nBandaranayake WM (1998) Traditional medicinal uses of mangroves. Mang Salt Mars 2:133–148\nBandaranayake WM (2002) Bioactivities: bioactive compounds and chemical constituents of mangrove plants. Wetl Ecol Manag 10:421–452\nPadmakumar K (1988) Bioactive substances from marine algae and mangroves. Ph.D Thesis, Annamalai University, Parangipettai p. 81\nSakagami H, Kashimita M, Toguchi M, Satoh K, Odanaka Y, Ida Y, Premanathan M, Arakaki R, Kathiresan K, Nakashma H, Komatsu N, Fujimarki M, Yoshihara M (1998) Radical modulation activity of lignins from a mangrove plant, Ceriops decandra (Griff.). Ding Hou In vivo 12:327–332\nKathiresan K, Veera Ravi A (1990) Seasonal changes in tannin content of mangrove leaves. Ind For 116:390–392\nKathiresan K (1995) Studies on tea from mangrove leaves. Environ Ecol 13:321–323\nLurie AD, Nintzal BB, Rippey RM (1977) Vascular volume and perfusion in hamster cheek pouches. Can Res 37:3484–3489\nShklar G (1972) Experimental oral pathology in the Syrian hamster. Prog Exp Tumor Res 16:518–538\nHolt JG, Krieg RN, Sneath PHA, Staley JT, Williams ST (1983) Bergey’s Manual System. Bacteriology 4:440\nOliver JD (1982) Instruments and methods: taxonomic scheme for the identification of marine bacteria. Deep Sea Res 29:795–798\nZeldow BJ (1961) Studies on the antibacterial action of human saliva: II observations on the mode of action of a lactobacillus bacteriocin. J Dent Res 40:446–453\nHirayama K, Rafter J (2000) The role of probiotic bacteria in cancer prevention. Micro Infec 2:681–686\nSingh J, Rivenson A, Tomita M, Shimamura S, Ishibashi N, Reddy BS (1997) Bifidobacterium longum, a lactic acid-producing intestinal bacterium inhibits colon cancer and modulates the intermediate biomarkers of colon carcinogenesis. Carcinogenesis 4:833–841\nBodana AR, Rao DR (1990) Antimutagenic activity of milk fermented by Streptococcus thermophilus and Lactobacillus bulgaricus. J Dairy Sci 73:3379\nMitsuoka T (1990) Bifidobacteria and their role in human health. J Ind Microbiol 6:263–267\nSpijkervet FKL, Saene JJ, Saene HK, Panders AK, Vermey A, Feilder V (1990) Chlorohexidine inactivation by saliva. Oral Surg Oral Med Oral Pathol 69:437–444\nKeyes PH (1960) The infectious and transmissible nature of experimental dental caries. Findings and implications. Arch Oral Biol 1:304–320\nDeVugst L, Vandamme EJ (1994) Bacteriocins of lactic acid bacteria. Microbiol Genet Appl London 75:140174–140179\nKathiresan K, Thiruneelakandan G (2008) Prospects of lactic acid bacteria of marine origin. Ind J Biotech 7:170–177\nWollowski I, Rechkemmer G, Pool-Zobel BL (2001) Protective role of probiotics and prebiotics in colon cancer. Am J Clin Nutri 73:451–455\nGoldin BR, Gorbach SL (1992) Probiotics for humans. In: Fuller R (ed) Probiotics. Champ Hall, London, pp 355–376\nDevine DA, Marsh PD (2009) Prospects for the development of probiotics and prebiotics for oral applications. J Oral Microbiol 1:1–11",{"VOID":2026},"10.1007\u002Fs12088-011-0096-3","2024-06-26T19:20:48.752+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12088-011-0096-3",[2030,2045,2058,2071],{"id":2031,"sortIndex":21,"researcher":20,"roles":2032,"affiliations":2033,"properties":2042,"displayName":2044,"givenName":20,"familyName":20},"7bf8b939-5c0e-4f57-be62-67a2ce86877a",[177],[2034],{"id":2035,"sortIndex":21,"affiliation":2036,"properties":20},"38c0d2ae-a1b4-48ad-ba25-fe4bb21d506a",{"id":2035,"createTime":20,"updateTime":20,"relativeEntities":2037,"slug":20,"properties":2038,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":2041,"statistic":20},[],{"title":2039},{"VI":2040},"CAS in Marine Biology, Annamalai University, Cuddalore, India",[],{"title":2043},{"VI":2044},"Natarajan Sithranga Boopathy",{"id":2046,"sortIndex":192,"researcher":20,"roles":2047,"affiliations":2048,"properties":2055,"displayName":2057,"givenName":20,"familyName":20},"d282c6a0-60c4-4c76-b11c-b35076797d62",[177],[2049],{"id":2035,"sortIndex":21,"affiliation":2050,"properties":20},{"id":2035,"createTime":20,"updateTime":20,"relativeEntities":2051,"slug":20,"properties":2052,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":2054,"statistic":20},[],{"title":2053},{"VI":2040},[],{"title":2056},{"VI":2057},"Kathiresan Kandasamy",{"id":2059,"sortIndex":206,"researcher":20,"roles":2060,"affiliations":2061,"properties":2068,"displayName":2070,"givenName":20,"familyName":20},"ee2a0730-e14f-4902-8c91-3bfee4c2d662",[177],[2062],{"id":2035,"sortIndex":21,"affiliation":2063,"properties":20},{"id":2035,"createTime":20,"updateTime":20,"relativeEntities":2064,"slug":20,"properties":2065,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":2067,"statistic":20},[],{"title":2066},{"VI":2040},[],{"title":2069},{"VI":2070},"Manivannan Subramanian",{"id":2072,"sortIndex":330,"researcher":20,"roles":2073,"affiliations":2074,"properties":2083,"displayName":2085,"givenName":20,"familyName":20},"9c8389e3-2b06-4a32-86fe-fa1f2d2bc990",[177],[2075],{"id":2076,"sortIndex":21,"affiliation":2077,"properties":20},"6b7fe5c2-c97a-4f53-b816-f26c434175ed",{"id":2076,"createTime":20,"updateTime":20,"relativeEntities":2078,"slug":20,"properties":2079,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":2082,"statistic":20},[],{"title":2080},{"VI":2081},"School of Biomedical Sciences, Jeju National University, Jeju, South Korea",[],{"title":2084},{"VI":2085},"Jeon You-Jin",{"url":2028,"publisher":2087,"properties":2129},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":2088,"slug":10,"properties":2089,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":2093,"manageAffiliations":2098,"indexDatabases":2109,"url":20,"thumbnailPath":20,"statistic":2124,"gsStatistic":20,"type":20,"analyzePriority":20},[],{"issn":2090,"title":2091,"eissn":2092},{"VOID":13},{"EN":15},{"VOID":17},[2094],{"id":24,"createTime":20,"updateTime":20,"relativeEntities":2095,"label":2096,"description":2097,"parentId":20,"standard":20,"scholarHubFieldId":20},[],{"EN":27},{},[2099,2104],{"id":31,"createTime":20,"updateTime":20,"relativeEntities":2100,"slug":20,"properties":2101,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":2103,"statistic":20},[],{"title":2102},{"EN":35},[],{"id":38,"createTime":20,"updateTime":20,"relativeEntities":2105,"slug":20,"properties":2106,"entityType":20,"verifyStatus":20,"verifyTime":20,"verifyNote":20,"languages":20,"translateLanguages":20,"viewCount":20,"url":20,"parentIds":2108,"statistic":20},[],{"title":2107},{"EN":42},[44],[2110,2117],{"id":47,"indexDatabase":2111,"url":58,"indexYears":59,"academicFieldIds":2116,"indexDatabaseRanking":62},{"id":49,"createTime":20,"updateTime":20,"relativeEntities":2112,"label":2113,"description":2114,"key":55,"publicationTags":2115,"standard":20},[],{"EN":52,"VI":52},{"EN":52,"VI":54},[57],[61],{"id":64,"indexDatabase":2118,"url":77,"indexYears":20,"academicFieldIds":2123,"indexDatabaseRanking":20},{"id":66,"createTime":20,"updateTime":20,"relativeEntities":2119,"label":2120,"description":2121,"key":73,"publicationTags":2122,"standard":20},[],{"EN":69,"VI":69},{"EN":71,"VI":72},[75,76],[79,80],{"impactFactor":21,"impactFactorByYear":2125,"i10Index":94,"i10IndexLast5Year":95,"totalPublication":96,"totalPublicationByYear":2126,"totalCitation":110,"totalCitationByYear":2127,"totalCitationPerPublication":126,"totalCitationPerPublicationByYear":2128,"hindexLast5Year":145,"hindex":145},{"2012":83,"2013":84,"2014":85,"2015":85,"2016":86,"2017":87,"2018":88,"2019":89,"2020":90,"2021":91,"2022":92,"2023":93},{"2007":98,"2008":99,"2009":100,"2010":101,"2011":102,"2012":103,"2013":104,"2014":105,"2015":106,"2016":100,"2017":107,"2018":107,"2019":101,"2020":99,"2021":107,"2022":108,"2023":109,"2024":100},{"2007":112,"2008":113,"2009":114,"2010":115,"2011":116,"2012":117,"2013":118,"2014":102,"2015":119,"2016":120,"2017":121,"2018":122,"2019":123,"2020":107,"2021":100,"2022":124,"2023":125},{"2007":128,"2008":129,"2009":130,"2010":131,"2011":132,"2012":133,"2013":134,"2014":135,"2015":136,"2016":137,"2017":138,"2018":139,"2019":140,"2020":141,"2021":142,"2022":143,"2023":144},{"pages":2130,"volume":2132},{"VOID":2131},"338-344",{"VOID":2133},"51","2011-02-27",2011,"DONE_GET_PLATFORM_ID",[62,75],{"id":2139,"createTime":2140,"updateTime":2141,"relativeEntities":2142,"slug":2143,"properties":2144,"entityType":166,"verifyStatus":167,"verifyTime":2155,"verifyNote":169,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":2156,"fullTextUrl":20,"authors":2157,"publicationType":218,"publisherRelationship":2206,"citationCount":21,"citationInfo":2254,"publishDate":2257,"publishYear":2255,"citationAnalyzeStatus":19,"lastCitationAnalyze":2141,"indexDatabases":2258,"openAccess":20,"references":20,"isForceReanalyzing":270},"39650d20-1680-4ae0-80f9-7a349725147a","2024-02-06T08:47:11.536+00:00","2026-05-22T02:54:28.554+00:00",[],"Extracellular-Synthesis-and-Characterization-of-Gold-Nanoparticles-Using-Mycobacterium-sp-BRS2A-AR2-Isolated-from-the-Aerial-Roots-of-the-Ghanaian-Mangrove-Plant-Rhizophora-racemosa",{"abstract":2145,"title":2147,"gsPaper":2149,"references":2151,"doi":2153},{"EN":2146},"Through the use of genomes that have undergone millions of years of evolution, marine Actinobacteria are known to have adapted to rapidly changing environmental pressures. The result is a huge chemical and biological diversity among marine Actinobacteria. It is gradually becoming a known fact that, marine Actinobacteria have the capability to produce nanoparticles which have reasonable sizes and structures with possible applications in biotechnology and pharmacology. Mycobacterium sp. BRS2A-AR2 was isolated from the aerial roots of the mangrove plant Rhizophora racemosa. The Mycobacterium was demonstrated for the first time ever to produce AuNPs with sizes that range between 5 and 55 nm. The highest level absorbance of the biosynthesized AuNPs was typical for actinobacterial strains (2.881 at 545 nm). The polydispersity index was measured as 0.207 in DLS and the zeta potential was negatively charged (− 28.3 mV). Significant vibration stretches were seen at 3314, 2358, 1635 and 667 cm−1 in FT-IR spectra. This demonstrated the possible use of small aliphatic compounds containing –COOH, –OH, –Cl and –NH2 functional groups in the stabilization of the AuNPs. The effect of the biosynthesized AuNPs on HUVEC and HeLA cell lines was measured at 48 h. IC50 values were determined at 3500 µg\u002Fml concentration for HUVEC and HeLA cell lines at 45.25 and 53.41% respectively.",{"EN":2148},"Extracellular Synthesis and Characterization of Gold Nanoparticles Using Mycobacterium sp. BRS2A-AR2 Isolated from the Aerial Roots of the Ghanaian Mangrove Plant, Rhizophora racemosa",{"VOID":2150},"[\"15189239569867127058\"]",{"VOID":2152},"Narayanan KB, Sakthivel N (2010) Biological synthesis of metal nanoparticles by microbes. Adv Coll Interface Sci 156(1–2):1–13. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.cis.2010.02.001\nStark WJ, Stoessel PR, Wohlleben W, Hafner A (2015) Industrial applications of nanoparticles. Chem Soc Rev 44(16):5793–5805. https:\u002F\u002Fdoi.org\u002F10.1039\u002Fc4cs00362d\nBaetke SC, Lammers T, Kiessling F (2015) Applications of nanoparticles for diagnosis and therapy of cancer. Br J Radiol 88(1054):20150207. https:\u002F\u002Fdoi.org\u002F10.1259\u002Fbjr.20150207\nDiao F, Wang Y (2017) Transition metal oxide nanostructures: premeditated fabrication and applications in electronic and photonic devices. J Mater Sci 53(6):4334–4359. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10853-017-1862-3\nMartins M, Mourato C, Sanches S, Noronha JP, Crespo MT, Pereira IA (2017) Biogenic platinum and palladium nanoparticles as new catalysts for the removal of pharmaceutical compounds. Water Res 108:160–168. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.watres.2016.10.071\nPatel SKS, Lee J-K, Kalia VC (2017) Nanoparticles in biological hydrogen production: an overview. Indian J Microbiol. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs12088-017-0678-9\nPugazhendhi S, Kirubha E, Palanisamy PK, Gopalakrishnan R (2015) Synthesis and characterization of silver nanoparticles from Alpinia calcarata by Green approach and its applications in bactericidal and nonlinear optics. Appl Surf Sci 357:1801–1808. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.apsusc.2015.09.237\nDe Sio L, Placido T, Comparelli R, Lucia Curri M, Striccoli M, Tabiryan N, Bunning TJ (2015) Next-generation thermo-plasmonic technologies and plasmonic nanoparticles in optoelectronics. Prog Quantum Electron 41:23–70. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.pquantelec.2015.03.001\nPatel SK, Choi SH, Kang YC, Lee JK (2016) Large-scale aerosol-assisted synthesis of biofriendly Fe(2)O(3) yolk-shell particles: a promising support for enzyme immobilization. Nanoscale 8(12):6728–6738. https:\u002F\u002Fdoi.org\u002F10.1039\u002Fc6nr00346j\nPatel SK, Choi SH, Kang YC, Lee JK (2017) Eco-friendly composite of Fe3O4-reduced graphene oxide particles for efficient enzyme immobilization. ACS Appl Mater Interfaces 9(3):2213–2222. https:\u002F\u002Fdoi.org\u002F10.1021\u002Facsami.6b05165\nOtari SV, Kumar M, Anwar MZ, Thorat ND, Patel SKS, Lee D, Lee JH, Lee JK, Kang YC, Zhang L (2017) Rapid synthesis and decoration of reduced graphene oxide with gold nanoparticles by thermostable peptides for memory device and photothermal applications. Sci Rep 7(1):10980. https:\u002F\u002Fdoi.org\u002F10.1038\u002Fs41598-017-10777-1\nOtari SV, Patel SKS, Jeong J-H, Lee JH, Lee J-K (2016) A green chemistry approach for synthesizing thermostable antimicrobial peptide-coated gold nanoparticles immobilized in an alginate biohydrogel. Rsc Adv 6(90):86808–86816. https:\u002F\u002Fdoi.org\u002F10.1039\u002Fc6ra14688k\nKhan ME, Khan MM, Cho MH (2015) Green synthesis, photocatalytic and photoelectrochemical performance of an Au–Graphene nanocomposite. Rsc Adv 5(34):26897–26904. https:\u002F\u002Fdoi.org\u002F10.1039\u002Fc5ra01864a\nHulkoti NI, Taranath TC (2014) Biosynthesis of nanoparticles using microbes—a review. Colloids Surf B 121:474–483. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.colsurfb.2014.05.027\nGolinska P, Wypij M, Ingle AP, Gupta I, Dahm H, Rai M (2014) Biogenic synthesis of metal nanoparticles from actinomycetes: biomedical applications and cytotoxicity. Appl Microbiol Biotechnol 98(19):8083–8097. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs00253-014-5953-7\nThakkar KN, Mhatre SS, Parikh RY (2010) Biological synthesis of metallic nanoparticles. Nanomed-Uk 6(2):257–262. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.nano.2009.07.002\nBarka EA, Vatsa P, Sanchez L, Gaveau-Vaillant N, Jacquard C, Klenk HP, Clement C, Ouhdouch Y, van Wezel GP (2016) Taxonomy, physiology, and natural products of actinobacteria. Microbiol Mol Biol Rev MMBR 80(1):1–43. https:\u002F\u002Fdoi.org\u002F10.1128\u002FMMBR.00019-15\nGoodfellow M, Williams ST (1983) Ecology of actinomycetes. Annu Rev Microbiol 37:189–216. https:\u002F\u002Fdoi.org\u002F10.1146\u002Fannurev.mi.37.100183.001201\nRamesh S, Jayaprakashvel M, Mathivanan N (2006) Microbial status in seawater and coastal sediments during pre- and post-tsunami periods in the Bay of Bengal, India. Mar Ecol 27(3):198–203. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fj.1439-0485.2006.00110.x\nRamesh S, Mathivanan N (2009) Screening of marine actinomycetes isolated from the Bay of Bengal, India for antimicrobial activity and industrial enzymes. World J Microbiol Biotechnol 25(12):2103–2111. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs11274-009-0113-4\nZhang H, Zhang W, Jin Y, Jin M, Yu X (2008) A comparative study on the phylogenetic diversity of culturable actinobacteria isolated from five marine sponge species. Antonie Van Leeuwenhoek 93(3):241–248. https:\u002F\u002Fdoi.org\u002F10.1007\u002Fs10482-007-9196-9\nDas M, Royer TV, Leff LG (2007) Diversity of fungi, bacteria, and actinomycetes on leaves decomposing in a stream. Appl Environ Microbiol 73(3):756–767. https:\u002F\u002Fdoi.org\u002F10.1128\u002FAEM.01170-06\nKarthik L, Kumar G, Keswani T, Bhattacharyya A, Reddy BP, Rao KVB (2013) Marine actinobacterial mediated gold nanoparticles synthesis and their antimalarial activity. Nanomed-Nanotechnol 9(7):951–960. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.nano.2013.02.002\nManivasagan P, Venkatesan J, Kang KH, Sivakumar K, Park SJ, Kim SK (2015) Production of alpha-amylase for the biosynthesis of gold nanoparticles using Streptomyces sp. MBRC-82. Int J Biol Macromol 72:71–78. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ijbiomac.2014.07.045\nManivasagan P, Venkatesan J, Senthilkumar K, Sivakumar K, Kim SK (2013) Biosynthesis, antimicrobial and cytotoxic effect of silver nanoparticles using a novel nocardiopsis sp MBRC-1. Biomed Res Int. https:\u002F\u002Fdoi.org\u002F10.1155\u002F2013\u002F287638\nSingh R, Nawale LU, Arkile M, Shedbalkar UU, Wadhwani SA, Sarkar D, Chopade BA (2015) Chemical and biological metal nanoparticles as antimycobacterial agents: a comparative study. Int J Antimicrob Agents 46(2):183–188. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ijantimicag.2015.03.014\nMansour A, Tammam S, Althani A, Azzazy HME (2017) A single tube system for the detection of Mycobacterium tuberculosis DNA using gold nanoparticles based FRET assay. J Microbiol Methods 139:165–167. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.mimet.2017.06.001\nMalhotra A, Dolma K, Kaur N, Rathore YS, Ashish Mayilraj S, Choudhury AR (2013) Biosynthesis of gold and silver nanoparticles using a novel marine strain of Stenotrophomonas. Bioresour Technol 142:727–731. https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.biortech.2013.05.109\nLane DJ (1991) 16S\u002F23S rRNA sequencing. Nucleic acid techniques in bacterial systematics. Wiley, Chichester, pp 115–175\nKim OS, Cho YJ, Lee K, Yoon SH, Kim M, Na H, Park SC, Jeon YS, Lee JH, Yi H, Won S, Chun J (2012) Introducing EzTaxon-e: a prokaryotic 16S rRNA gene sequence database with phylotypes that represent uncultured species. Int J Syst Evol Microbiol 62:716–721. https:\u002F\u002Fdoi.org\u002F10.1099\u002Fijs.0.038075-0\nTamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: molecular evolutionary genetics analysis version 6.0. 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