Antibacterial, Anticancer and Neuroprotective Activities of Rare Actinobacteria from Mangrove Forest Soils
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Qin S, Li J, Chen HH, Zhao GZ, Zhu WY, Jiang CL, Xu LH, Li WJ (2009) Isolation, diversity, and antimicrobial activity of rare actinobacteria from medicinal plants of tropical rain forests in Xishuangbanna, China. Appl Environ Microbiol 75:6176–6186. doi: 10.1128/AEM.01034-09
Manivasagan P, Venkatesan J, Sivakumar K, Kim SK (2013) Marine actinobacterial metabolites: current status and future perspectives. Microbiol Res 168:311–332. doi: 10.1016/j.micres.2013.02.002
Subramani R, Aalbersberg W (2012) Marine actinomycetes: an ongoing source of novel bioactive metabolites. Microbiol Res 167:571–580. doi: 10.1016/j.micres.2012.06.005
Lee LH, Zainal N, Azman AS, Eng SK, Ab Mutalib NS, Yin WF, Chan KG (2014) Streptomyces pluripotens sp. nov., a bacteriocin-producing streptomycete that inhibits methicillin-resistant Staphylococcus aureus. Int J Syst Evol Microbiol 64:3297–3306. doi: 10.1099/ijs.0.065045-0
Ser HL, Ab Mutalib NS, Yin WF, Chan KG, Goh BH, Lee LH (2015) Evaluation of antioxidative and cytotoxic activities of Streptomyces pluripotens MUSC 137 isolated from mangrove soil in Malaysia. Front Microbiol 6:1398. doi: 10.3389/fmicb.2015.01398
Tan LTH, Ser HL, Yin WF, Chan KG, Lee LH, Goh BH (2015) Investigation of antioxidative and anticancer potentials of Streptomyces sp. MUM256 isolated from Malaysia mangrove soil. Front Microbiol 6:1316. doi: 10.3389/fmicb.2015.01316
Ser HL, Law JWF, Chaiyakunapruk N, Jacob SA, Palanisamy UD, Chan KG, Goh BH, Lee LH (2016) Fermentation conditions that affect clavulanic acid production in Streptomyces clavuligerus: a systematic review. Front Microbiol 7:522. doi: 10.3389/fmicb.2016.00522
Tan LTH, Chan KG, Lee LH, Goh BH (2016) Streptomyces bacteria as potential probiotics in aquaculture. Front Microbiol 7:79. doi: 10.3389/fmicb.2016.00079
Hong K, Gao AH, Xie QY, Gao H, Zhuang L, Lin HP, Yu HP, Li J, Yao XS, Goodfellow M, Ruan JS (2009) Actinomycetes for marine drug discovery isolated from mangrove soils and plants in China. Mar Drugs 7:24–44. doi: 10.3390/md7010024
Lee LH, Zainal N, Azman AS, Eng SK, Goh BH, Yin WF, Ab. Mutalib NS, Chan KG (2014a) Diversity and antimicrobial activities of actinobacteria isolated from tropical mangrove sediments in Malaysia. Sci World J 2014: Article ID: 698178
Hamedi J, Imanparast S, Mohammadipanah F (2015) Molecular, chemical and biological screening of soil actinomycete isolates in seeking bioactive peptide metabolites. Iran J Microbiol 7:23–30
Neha S, Sandeep S (2014) Microbial secondary metabolites as potential anti-infective agents. Int J Pharm Sci Rev Res 2:767–773
Azman AS, Othman I, Velu SS, Chan KG, Lee LH (2015) Mangrove rare actinobacteria: taxonomy, natural compound, and discovery of bioactivity. Front Microbiol 6:856. doi: 10.3389/fmicb.2015.00856
Tiwari K, Gupta RK (2012) Rare actinomycetes: a potential storehouse for novel antibiotics. Crit Rev Biotechnol 32:108–132. doi: 10.3109/07388551.2011.562482
Goodfellow M (2010) Selective isolation of Actinobacteria. In: Baltz RH, Davies J, Demain AL (eds) Manual of industrial microbiology and biotechnology. ASM, Washington, pp 13–27
Xu DB, Ye WW, Han Y, Deng ZX, Hong K (2014) Natural products from mangrove actinomycetes. Mar Drugs 12:2590–2613. doi: 10.3390/md12052590
Lee LH, Azman AS, Zainal N, Eng SK, Ab Mutalib NS, Yin WF, Chan KG (2014) Microbacterium mangrovi sp. nov., an amylolytic actinobacterium isolated from mangrove forest soil. Int J Syst Evol Microbiol 64:3513–3519. doi: 10.1099/ijs.0.062414-0
Lee LH, Azman AS, Zainal N, Yin WF, Mutalib NS, Chan KG (2015) Sinomonas humi sp. nov., an amylolytic actinobacterium isolated from mangrove forest soil. Int J Syst Evol Microbiol 65:996–1002. doi: 10.1099/ijs.0.000053
Azman AS, Zainal N, Ab Mutalib NS, Yin WF, Chan KG, Lee LH (2015) Monashia flava gen. nov., sp. nov., a novel actinobacterium of the family Intrasporangiaceae. Int J Syst Evol Microbiol. doi: 10.1099/ijsem.0.000753
Mangamuri UK, Vijayalakshmi M, Poda S, Manavathi B, Bhujangarao C, Venkateswarlu Y (2015) Bioactive metabolites produced by Pseudonocardia endophytica VUK-10 from mangrove sediments: isolation, chemical structure determination and bioactivity. J Microbiol Biotechnol 25:629–636
Janardhan A, Kumar AP, Viswanath B, Saigopal DVR, Narasimha G (2014) Production of bioactive compounds by actinomycetes and their antioxidant properties. Biotechnol Res Int 55:1897–1901
Williams PG, Buchanan GO, Feling RH, Kauffman CA, Jensen PR, Fenical W (2005) New cytotoxic salinosporamides from the marine Actinomycete Salinispora tropica. J Org Chem 70:6196–6203. doi: 10.1021/jo050511+
Lee LH, Cheah YK, Sidik SM, Ab Mutalib NS, Tang YL, Lin HP, Hong K (2012) Molecular characterization of Antarctic actinobacteria and screening for antibacterial metabolite production. World J Microbiol Biotechnol 28:2125–2137
Ser HL, Palanisamy UD, Yin WF, Chan KG, Goh BH, Lee LH (2016) Streptomyces malaysiense sp. nov.: a novel Malaysian mangrove soil actinobacterium with antioxidative activity and cytotoxic potential against human cancer cell lines. Sci Rep 6:24247. doi: 10.1038/srep24247
Wiegand I, Hilpert K, Hancock RE (2008) Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances. Nat Protoc 3:163–175. doi: 10.1038/nprot.2007.521
Supriady H, Kamarudin MNA, Chan CK, Goh BH, Kadir HA (2015) SMEAF attenuates the production of pro-inflammatory mediators through the inactivation of Akt-dependent NF-κB, p38 and ERK1/2 pathways in LPS-stimulated BV-2 microglial cells. J Funct Foods 17:434–448. doi: 10.1016/j.jff.2015.05.042
Ser HL, Zainal N, Palanisamy UD, Goh BH, Chan KG, Lee LH (2015) Streptomyces gilvigriseus sp. nov., a novel actinobaterium isolated from mangrove forest soil. Antonie Van Leeuwenhoek 107:1369–1378. doi: 10.1007/s10482-015-0431-5
Ocampo PS, Lazar V, Papp B, Arnoldini M, Wiesch PA, Busa-Fekete R, Fekete G, Pal C, Ackermann M, Bonhoeffer S (2014) Antagonism between bacteriostatic and bactericidal antibiotics is prevalent. Antimicrob Agents Chemother 58:4573–4582. doi: 10.1128/aac.02463-14
Pankey GA, Sabath LD (2004) Clinical relevance of bacteriostatic versus bactericidal mechanisms of action in the treatment of Gram-positive bacterial infections. Clin Infect Dis 38:864–870. doi: 10.1086/381972
Wu D, Yotnda P (2011) Induction and testing of hypoxia in cell culture. J Vis Exp 54:2899. doi: 10.3791/2899
Zhang Y-B, Wang X, Meister EA, Gong K-R, Yan S-C, Lu G-W, Ji X-M, Shao G (2014) The effects of CoCl(2) on HIF-1α protein under experimental conditions of autoprogressive hypoxia using mouse models. Int J Mol Sci 15:10999–11012. doi: 10.3390/ijms150610999
Grasselli F, Basini G, Bussolati S, Bianco F (2005) Cobalt chloride, a hypoxia-mimicking agent, modulates redox status and functional parameters of cultured swine granulosa cells. Reprod Fertil Dev 17:715–720
Yu X, Gao D (2013) Overexpression of cytoglobin gene inhibits hypoxic injury to SH-SY5Y neuroblastoma cells. Neural Regen Res 8:2198–2203. doi: 10.3969/j.issn.1673-5374.2013.23.010
Lee SG, Lee H, Rho HM (2001) Transcriptional repression of the human p53 gene by cobalt chloride mimicking hypoxia. FEBS Lett 507:259–263
Vengellur A, LaPres JJ (2004) The role of hypoxia inducible factor 1alpha in cobalt chloride induced cell death in mouse embryonic fibroblasts. Toxicol Sci 82:638–646. doi: 10.1093/toxsci/kfh278
Chow JM, Shen SC, Huan SK, Lin HY, Chen YC (2005) Quercetin, but not rutin and quercitrin, prevention of H2O2-induced apoptosis via anti-oxidant activity and heme oxygenase 1 gene expression in macrophages. Biochem Pharmacol 69:1839–1851. doi: 10.1016/j.bcp.2005.03.017
Shivapriya S, Ilango K, Agrawal A, Dubey GP (2014) Effect of Hippophae rhamnoides on cognitive enhancement via neurochemical modulation in scopolamine induced Sprague Dawley rats. Int J Pharm Sci Res 5:4153–4158
Triana-Vidal LE, Carvajal-Varona SM (2013) Protective effect of galantamine against oxidative damage using human lymphocytes: a novel in vitro model. Arch Med Res 44:85–92. doi: 10.1016/j.arcmed.2013.01.001
Facecchia K, Fochesato LA, Ray SD, Stohs SJ, Pandey S (2011) Oxidative toxicity in neurodegenerative diseases: role of mitochondrial dysfunction and therapeutic strategies. J Toxicol 2011:683728. doi: 10.1155/2011/683728
Powers SK, Jackson MJ (2008) Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiol Rev 88:1243–1276. doi: 10.1152/physrev.00031.2007
Konyalioglu S, Armagan G, Yalcin A, Atalayin C, Dagci T (2013) Effects of resveratrol on hydrogen peroxide-induced oxidative stress in embryonic neural stem cells. Neural Regen Res 8:485–495. doi: 10.3969/j.issn.1673-5374.2013.06.001
Kuljis RO (2010) Integrative understanding of emergent brain properties, quantum brain hypotheses, and connectome alterations in dementia are key challenges to conquer Alzheimer’s disease. Front Neurol 1:15. doi: 10.3389/fneur.2010.00015
Salkovic-Petrisic M (2008) Amyloid cascade hypothesis: is it true for sporadic Alzheimer’s disease. Period Biol 110:17–25
Wang P, Jiang S, Cui Y, Yue Z, Su C, Sun J, Sheng S, Tian J (2011) The n-terminal 5-MER peptide analogue P165 of amyloid precursor protein exerts protective effects on SH-SY5Y cells and rat hippocampus neuronal synapses. Neuroscience 173:169–178. doi: 10.1016/j.neuroscience.2010.10.069
Saxena G, Singh SP, Agrawal R, Nath C (2008) Effect of donepezil and tacrine on oxidative stress in intracerebral streptozotocin-induced model of dementia in mice. Eur J Pharmacol 581:283–289. doi: 10.1016/j.ejphar.2007.12.009
Stuchbury G, Munch G (2005) Alzheimer’s associated inflammation, potential drug targets and future therapies. J Neural Transm 112:429–453. doi: 10.1007/s00702-004-0188-x
Mandelkow E, von Bergen M, Biernat J, Mandelkow EM (2007) Structural principles of tau and the paired helical filaments of Alzheimer’s disease. Brain Pathol 17:83–90. doi: 10.1111/j.1750-3639.2007.00053.x
Samy DM, Ismail CA, Nassra RA, Zeitoun TM, Nomair AM (2016) Downstream modulation of extrinsic apoptotic pathway in streptozotocin-induced Alzheimer’s dementia in rats: erythropoietin versus curcumin. Eur J Pharmacol 770:52–60. doi: 10.1016/j.ejphar.2015.11.046
Karanja E, Boga H, Muigai A, Wamunyokoli F, Kinyua J, Nonoh J (2010) Growth characteristics and production of secondary metabolites from selected novel Streptomyces species isolated from selected Kenyan national parks. Sci Conf Proc, pp 51–80. http://journals.jkuat.ac.ke/index.php/jscp/article/view/672
Jog R, Pandya M, Nareshkumar G, Rajkumar S (2014) Mechanism of phosphate solubilization and antifungal activity of Streptomyces spp. isolated from wheat roots and rhizosphere and their application in improving plant growth. Microbiology 160:778–788. doi: 10.1099/mic.0.074146-0
Pereira D, Valentão P, Pereira J, Andrade P (2009) Phenolics: from chemistry to biology. Molecules 14:2202–2211. doi: 10.3390/molecules14062202
Han XZ, Shen T, Lou HX (2007) Dietary polyphenols and their biological significance. Int J Mol Sci 8:950–988. doi: 10.3390/i8090950
Baidez AG, Gomez P, Del Rio JA, Ortuno A (2007) Dysfunctionality of the xylem in Olea europaea L. plants associated with the infection process by Verticillium dahliae Kleb: role of phenolic compounds in plant defense mechanism. J Agric Food Chem 55:3373–3377. doi: 10.1021/jf063166
Veeriah S, Kautenburger T, Habermann N, Sauer J, Dietrich H, Will F, Pool-Zobel BL (2006) Apple flavonoids inhibit growth of HT29 human colon cancer cells and modulate expression of genes involved in the biotransformation of xenobiotics. Mol Carcinogen 45:164–174. doi: 10.1002/mc.20158
Owen RW, Giacosa A, Hull WE, Haubner R, Spiegelhalder B, Bartsch H (2000) The antioxidant/anticancer potential of phenolic compounds isolated from olive oil. Eur J Cancer 36:1235–1247. doi: 10.1016/S0959-8049(00)00103-9
Lenartowicz P, Kafarski P, Lipok J (2015) The overporoduction of 2,4-DTBP accompanying to the lack of available form of phosphorus during the biodegradative utilization of aminophosphonates by Aspergillus terreus. Biodegradation 26:65–76. doi: 10.1007/s10532-014-9716-z
Varsha KK, Devendra L, Shilpa G, Priya S, Pandey A, Nampoothiri KM (2015) 2,4-Di-tert-butyl phenol as the antifungal, antioxidant bioactive purified from a newly isolated Lactococcus sp. Int J Food Microbiol 11:44–50. doi: 10.1016/j.ijfoodmicro.2015.06.025
Dharni S, Sanchita Maurya A, Samad A, Srivastava SK, Sharma A, Patra DD (2014) Purification, characterization, and in vitro activity of 2,4-Di-tert-butylphenol from Pseudomonas monteilii PsF84: conformational and molecular docking studies. J Agric Food Chem 62:6138–6146. doi: 10.1021/jf5001138
Yogeswari S, Ramalakshmi S, Neelavathy R, Muthumary J (2012) Identification and comparative studies of different volatile fractions from Monochaetia kansensis by GCMS. Glob J Pharmacol 6:65–71
Premkumar T, Govindarajan S (2005) Antimicrobial study of pyrazine, pyrazole and imidazole carboxylic acids and their hydrazinium salts. World J Microbiol Biotech 21:479–480. doi: 10.1007/s11274-004-2041-7
Jia J, Zhang X, Hu YS, Wu Y, Wang QZ, Li NN, Wu CQ, Yu HX, Guo QC (2009) Protective effect of tetraethyl pyrazine against focal cerebral ischemia/reperfusion injury in rats: therapeutic time window and its mechanism. Thromb Res 123:727–730. doi: 10.1016/j.thromres.2008.11.004
Baldwin MV, Arikkatt SD, Sindhu TJ, Chanran M, Bhat AR, Krishnakumar K (2013) A review of biological potential of pyrazine and related heterocyclic compounds. World J Pharm Pharmaceut Sci 3:1124–1132
Ser HL, Tan LTH, Palanisamy UD, Abd Malek SN, Yin WF, Chan KG, Goh BH, Lee LH (2016) Streptomyces antioxidans sp. nov., a novel mangrove soil actinobacterium with antioxidative and neuroprotective potentials. Front Microbiol 7:899. doi: 10.3389/fmicb.2016.00899
Wang DH, Tao WY (2009) Antitumor activity in vitro and volatile components of metabolites from myxobacteria Stigmatella WXNXJ-B. Afr J Microbiol Res 3:755–760
Ser HL, Ab Mutalib NS, Yin WF, Chan KG, Goh BH, Lee LH (2015) Evaluation of antioxidative and cytotoxic activities of Streptomyces pluripotens MUSC 137 isolated from mangrove soil in Malaysia. Front Microbiol 6:1398. doi: 10.3389/fmicb.2015.01398
Sharma P, Kalita MC, Thakur D (2016) Broad spectrum antimicrobial activity of forest-derived soil Actinomycete, Nocardia sp. PB-52. Front Microbiol 7:347. doi: 10.3389/fmicb.2016.00347
Gopi M, Dhayanithi NB, Devi KN, Kumar TTA (2014) Marine natural product, Pyrrolo [1,2-a] pyrazine–1,4-dione, hexahydro-(C7H10N2O2) of antioxidant properties from Bacillus species at Lakshadweep archipelago. J Coast Life Med 2:632–637. doi: 10.12980/jclm.2.201414j40
Gohar YM, El-Naggar MMA, Soliman MK, Barakat KM (2010) Characterization of marine Burkholderia cepacia antibacterial agents. J Nat Prod 3:86–94
Yoon GY, Lee YS, Lee SY, Park RD, Hyun HN, Nam Y, Kim KY (2012) Effects on Meloidogyne incognita of chitinase, glucanase and a secondary metabolite from Streptomyces cacaoi GY525. Nematology 14:175–184. doi: 10.1163/138855411x584124
Manimaran M, Gopal JV, Kannabiran K (2015) Antibacterial activity of Streptomyces sp. VITMK1 isolated from mangrove soil of Pichavaram, Tamil Nadu, India. Proc Indian Acad Sci Sect B. doi: 10.1007/s40011-015-0619-5
Narasaiah BC, Leelavathi V, Sudhakar G, Mariyadasu P, Swapna G, Manne AK (2014) Isolation and structural confirmation of bioactive compounds produced by the strain Streptomyces albus CN-4. IOSR J Pharm Biol Sci 9:49–54. doi: 10.9790/3008-09654954
Melo IS, Santos SN, Rosa LH, Parma MM, Silva LJ, Queiroz SCN, Pellizari VH (2013) Isolation and biological activities of an endophytic Mortierella alpine strain from the Antarctic moss Schistidium antarctici. Extremophiles 18:15. doi: 10.1007/s00792-013-0588-7
Hong S, Moon BH, Yong Y, Shin SY, Lee YH, Lim Y (2008) Inhibitory effect against Akt of cyclic dipeptides isolated from Bacillus sp. J Microbiol Biotechnol 18:682–685
Narendhran S, Rajiv P, Vanathi P, Sivaraj R (2014) Spectroscopic analysis of bioactive compounds from Streptomyces cavouresis KU-V39: evaluation of antioxidant and cytotoxicity activity. Int J Pharm Pharmaceut Sci 6:322