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This study was triggered by the characterization of a 9‐kDa LTP from \u003Cjats:italic>Capsicum annuum\u003C\u002Fjats:italic> seeds that we call \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub>. \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub> was repurified, and in the last chromatographic purification step, propanol was used as the solvent in place of acetonitrile to maintain the protein's biological activity. Bidimensional electrophoresis of the 9‐kDa band, which corresponds to the purified \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub>, showed the presence of three isoforms with isoelectric points (pIs) of 6.0, 8.5 and 9.5. Circular dichroism (CD) analysis suggested a predominance of \u003Cjats:italic>α\u003C\u002Fjats:italic>‐helices, as expected for the structure of an LTP family member. LTPs immunorelated to \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub> from \u003Cjats:italic>C. annuum\u003C\u002Fjats:italic> were also detected by western blotting in exudates released from \u003Cjats:italic>C. annuum\u003C\u002Fjats:italic> seeds and also in other \u003Cjats:italic>Capsicum\u003C\u002Fjats:italic> species. The tissue and subcellular localization of \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub> indicated that it was mainly localized within dense vesicles. In addition, isolated \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub> exhibited antifungal activity against \u003Cjats:italic>Colletotrichum lindemunthianum\u003C\u002Fjats:italic>, and especially against \u003Cjats:italic>Candida tropicalis\u003C\u002Fjats:italic>, causing several morphological changes to the cells including the formation of pseudohyphae. \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub> also caused the yeast plasma membrane to be permeable to the dye SYTOX green, as verified by fluorescence microscopy. We also found that \u003Cjats:italic>Ca\u003C\u002Fjats:italic>‐LTP\u003Cjats:sub>1\u003C\u002Fjats:sub> is able to inhibit mammalian \u003Cjats:italic>α\u003C\u002Fjats:italic>‐amylase activity in vitro.\u003C\u002Fjats:p>",{"EN":505},"Characterisation, immunolocalisation and antifungal activity of a lipid transfer protein from chili pepper (\u003Ci>Capsicum annuum\u003C\u002Fi>) seeds with novel \u003Ci>α\u003C\u002Fi>‐amylase inhibitory 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However, two examples of environmental stresses that drastically regulate soybean growth are low light and high‐temperature. Emerging evidence suggests a possible interconnection between these two environmental stimuli. Low light and high‐temperature as individual factors have been reported to regulate plant hypocotyl elongation. However, their interactive signal effect on soybean growth and development remains largely unclear. Here, we report that gibberellins (GAs) and auxin are required for soybean hypocotyl elongation under low light and high‐temperature interaction. Our analysis indicated that low light and high‐temperature interaction enhanced the regulation of soybean hypocotyl elongation and that the endogenous GA\u003Cjats:sub>3\u003C\u002Fjats:sub>, GA\u003Cjats:sub>7\u003C\u002Fjats:sub>, indole‐3‐acetic acid (IAA), and indole‐3‐pyruvate (IPA) contents significantly increased. Again, analysis of the effect of exogenous phytohormones and biosynthesis inhibitors treatments showed that exogenous GA, IAA, and paclobutrazol (PAC), 2, 3, 5,‐triiodobenzoic acid (TIBA) treatments significantly regulated soybean seedlings growth under low light and high‐temperature interaction. Further qRT‐PCR analysis showed that the expression level of GA biosynthesis pathway genes (\u003Cjats:italic>GmGA3ox1, GmGA3ox2\u003C\u002Fjats:italic> and \u003Cjats:italic>GmGA3\u003C\u002Fjats:italic>) and auxin biosynthesis pathway genes (\u003Cjats:italic>GmYUCCA3\u003C\u002Fjats:italic>, \u003Cjats:italic>GmYUCCA5\u003C\u002Fjats:italic> and \u003Cjats:italic>GmYUCCA7\u003C\u002Fjats:italic>) significantly increased under (i) low light and high‐temperature interaction and (ii) exogenous GA and IAA treatments. 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H., 1984, Storage Carbohydrates in Vascular Plants. Distribution, Physiology and Metabolism, 75",{},{"id":24,"text":2070,"url":24,"identifiers":2388},{"doi":2070},{"id":24,"text":2390,"url":24,"identifiers":2391},"10.1104\u002Fpp.76.1.45",{"doi":2390},{"id":24,"text":2393,"url":24,"identifiers":2394},"10.1007\u002FBF00398269",{"doi":2393},{"id":24,"text":2396,"url":24,"identifiers":2397},"10.1007\u002FBF00027291",{"doi":2396},{"id":24,"text":2399,"url":24,"identifiers":2400},"10.1111\u002Fj.1365-3040.1985.tb01203.x",{"doi":2399},{"id":24,"text":2402,"url":24,"identifiers":2403},"10.1111\u002Fj.1399-3054.1983.tb02769.x",{"doi":2402},{"id":24,"text":2405,"url":24,"identifiers":2406},"Wareing P. F., 1975, Photosynthesis and Productivity in Different Environments, 481",{},{"id":24,"text":2079,"url":24,"identifiers":2408},{"doi":2079},{"id":24,"text":2082,"url":24,"identifiers":2410},{"doi":2082},{"id":24,"text":2085,"url":24,"identifiers":2412},{"doi":2085},{"id":24,"text":2414,"url":24,"identifiers":2415},"10.1007\u002FBF00027290",{"doi":2414},{"id":24,"text":2417,"url":24,"identifiers":2418},"Wolswinkel P., 1985, Turgor‐sensitive transport in developing seeds of legumes, Plant Physiol., 77",{},{"id":24,"text":2420,"url":24,"identifiers":2421},"Wolswinkel P., 1985, Biology and Control of Parasitic Weeds. Alectra, Orobanche and Cuscuta",{},{"id":24,"text":2088,"url":24,"identifiers":2423},{"doi":2088},{"id":24,"text":2091,"url":24,"identifiers":2425},{"doi":2091},{"id":24,"text":1910,"url":24,"identifiers":2427},{"doi":1910},{"id":24,"text":2429,"url":24,"identifiers":2430},"10.1093\u002Fjxb\u002F36.3.359",{"doi":2429},{"id":24,"text":2432,"url":24,"identifiers":2433},"Wolswinkel P., 1985, Effect of potassium on sucrose and amino acid release from the seed coat of developing seeds of Pisum sativum, Ann. Bot., 56, 35, 10.1093\u002Foxfordjournals.aob.a086992",{"doi":2434},"10.1093\u002Foxfordjournals.aob.a086992",{"id":24,"text":2094,"url":24,"identifiers":2436},{"doi":2094},{"id":24,"text":2438,"url":24,"identifiers":2439},"10.1104\u002Fpp.75.1.13",{"doi":2438},{"id":24,"text":2441,"url":24,"identifiers":2442},"10.1104\u002Fpp.64.5.837",{"doi":2441},{"id":24,"text":2444,"url":24,"identifiers":2445},"Zamski E., 1984, Turgor regulation of sucrose transport in sugarbeet taproot tissue, Plant Physiol., 75",{},{"id":2447,"createTime":2448,"updateTime":2448,"relativeEntities":2449,"slug":2450,"properties":2451,"entityType":262,"verifyStatus":263,"verifyTime":2448,"verifyNote":264,"syncStatus":23,"languages":2463,"translateLanguages":24,"viewCount":25,"primaryUrl":2464,"fullTextUrl":24,"authors":2465,"publicationType":326,"publisherRelationship":2485,"citationCount":162,"citationInfo":2522,"publishDate":2524,"publishYear":2525,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":2526,"isForceReanalyzing":490},"70cdbbb6-7cb2-4436-8f9e-4bd8c9da7506","2024-10-10T22:39:54.233+00:00",[],"Sucrose-release-from-soybean-leaf-slices",{"mag":2452,"keywords":2454,"openalex":2455,"abstract":2457,"title":2459,"doi":2461},{"VOID":2453},"2041032722",{},{"VOID":2456},"W2041032722",{"EN":2458},"\u003Cjats:p>The release of photosynthate from leaf slices of soybean [\u003Cjats:italic>Glycine max\u003C\u002Fjats:italic> (L.) Merr. cv. Ransom II], to a bathing medium was studied to ascertain how \u003Cjats:italic>p\u003C\u002Fjats:italic>‐chloromercuribenzenesulfonic acid (PCMBS) can both stimulate and inhibit sucrose release. Soybean leaf slices released photosynthate to a bathing medium at a rate that was approximately linear with time. The photosynthate released was about 20% ionic and 80% non‐ionic, and sucrose represented about 75% of the total. Removal of Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> from the medium increased the rate of release of all fractions, but amino acid release showed the largest increase. Sucrose was released at a rate estimated to be about 20% of the normal transport rate in intact leaves. The rate of sucrose uptake from 5 m\u003Cjats:italic>M\u003C\u002Fjats:italic> sucrose into soybean leaf slices was optimum at pH 6.3, and the rate of sucrose release was lowest at the same pH. However, sucrose uptake was found to be insignificant during release experiments. Sucrose release, but not amino acid release, was inhibited 75% by 1 m\u003Cjats:italic>M\u003C\u002Fjats:italic> PCMBS.\u003C\u002Fjats:p>\u003Cjats:p>The data support two components of sucrose release in leaves. The first is insensitive to the addition of PCMBS. This component probably represents leakage from phloem tissue. The second component is inhibited by PCMBS and probably represents release from the mesophyll. By comparing sucrose release from leaf slices of 12 different species of plants, 2 groups were found. In the first group, sucrose release was inhibited between 60 and 80% by PCMBS, and in the second group between 0% and 40%. The difference in the two groups can be explained by a relative difference in the size of the two components of sucrose release for each species.\u003C\u002Fjats:p>",{"EN":2460},"Sucrose release from soybean leaf slices",{"VOID":2462},"10.1111\u002Fj.1399-3054.1986.tb02427.x",[266],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1399-3054.1986.tb02427.x",[2466],{"id":2467,"sortIndex":25,"researcher":24,"roles":2468,"affiliations":2469,"properties":2480},"bde18581-e704-4391-b1e3-8981b8135ff9",[],[2470],{"id":2471,"sortIndex":25,"affiliation":2472,"properties":24},"adb76757-4ba0-4956-b543-6f6db053520f",{"id":2473,"createTime":2474,"updateTime":2474,"relativeEntities":2475,"slug":2476,"properties":2477,"entityType":77,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25},"44440b79-01e2-4256-a332-4522cb20eda2","2024-10-10T22:39:54.255+00:00",[],"U-S-Dept-of-Agriculture-Agricultural-Research-Service-Depts-of-Crop-Science-and-Botany-3127-Ligon-Street-North-Carolina-State-Univ-Raleigh-NC-27607-USA-",{"title":2478},{"EN":2479},"U. 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metabolic profile analysis will aid in the fundamental understanding of physiology. Here, we present a possible analysis workflow. Initially, the procedure to transform raw data into a data matrix containing relative metabolite levels for each sample is described. Given that, because of experimental issues in the technical equipment, the levels of some metabolites cannot be universally determined or that different experiments need to be compared, missing value estimation and normalization are presented as helpful preprocessing steps. Regression methods are presented in this review as tools to relate metabolite levels with other physiological properties like biomass and gene expression. As the number of measured metabolites often exceeds the number of samples, dimensionality reduction methods are required. Two of these methods are discussed in detail in this review. Throughout this article, practical examples illustrating the application of the aforementioned methods are given. We focus on the uncovering the relationship between metabolism and growth‐related properties.\u003C\u002Fjats:p>",{"EN":2582},"Metabolite profile analysis: from raw data to regression and 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in a variety of plant\u002Fpathogen systems. In particular, two species, hydrogen peroxide (H\u003Cjats:sub>2\u003C\u002Fjats:sub>O\u003Cjats:sub>2\u003C\u002Fjats:sub>) and the superoxide radical anion O\u003Cjats:sub>2\u003C\u002Fjats:sub>\u003Cjats:sup>−\u003C\u002Fjats:sup> have received considerable attention. H\u003Cjats:sub>2\u003C\u002Fjats:sub>O\u003Cjats:sub>2\u003C\u002Fjats:sub> and O\u003Cjats:sub>2\u003C\u002Fjats:sub>\u003Cjats:sup>−\u003C\u002Fjats:sup>, while acting directly as antimicrobial agents, may also serve as second messengers or catalysts in plants to activate a more diverse set of defense responses. Some of the better studied downstream responses promoted by AOS are (1) the cross‐linking of cell wall proteins, (2) the induction of defense‐related genes, (3) the stimulation of phytoalexin biosynthesis and (4) promotion of the hypersensitive response (HR).\u003C\u002Fjats:p>\u003Cjats:p>A useful model for studying the oxidative burst in plants is the neutrophil NADPH ox‐idase complex, the primary source of AOS production in mammals. Several of the subunits of the neutrophil NADPH oxidase complex have been immunologically identified in plants. Furthermore, many of the components known to be involved in the signal transduction pathway in neutrophils have also been found to play a role in the oxidative burst in plants. Just as various ligands activate the oxidase complex in neutrophils, several ligands (elicitors or pathogens) also lead to induction of the oxidative burst in plant cells. The similarities between the neutrophil and plant oxidative bursts will be elaborated in this review.\u003C\u002Fjats:p>\u003Cjats:p>Following stimulation with elicitors, different signal transduction pathways are activated in plants, depending on the source of elicitor used. While the identities and chronologies of the major intermediates in these pathways remain largely unknown, there is strong evidence at least for participation of phospholipases, H\u003Cjats:sup>+\u003C\u002Fjats:sup>\u002FK\u003Cjats:sup>+\u003C\u002Fjats:sup> exchange, Ca\u003Cjats:sup>2+\u003C\u002Fjats:sup> influxes, protein kinases and phosphatases, and GTP binding proteins. 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This study monitored seasonal changes in photosynthesis and photoprotection in an evergreen oak (\u003Cjats:italic>Cyclobalanopsis helferiana\u003C\u002Fjats:italic>) from one of these valleys for four years during which usual and abnormal drought occurred. In general, during the study period with decreasing xylem water potential (Ψx), photosynthetic gas exchange, quantum yield of photosystem II (PSII) photochemistry and activities of most of the measured antioxidant enzymes decreased, while activities of the xanthophyll cycle and associated non‐photochemical energy dissipation and glutathione peroxidase (GP) (EC 1.11.1.9) increased. In a fairly severe chill period, high concentration of reactive oxygen species induced high activities of most of the antioxidant enzymes and relatively stronger decrease in gas exchange. In the most severe dry period, even when predawn Ψx decreased down to −4 MPa, considerable Pn (maximum photosynthetic rate) (4 μmol m\u003Cjats:sup>–2\u003C\u002Fjats:sup> s\u003Cjats:sup>–1\u003C\u002Fjats:sup>) was still maintained in midmorning. At this time, most of the antioxidant enzyme activities decreased to the lowest values, whereas the xanthophyll cycle and associated non‐photochemical energy dissipation and GP activities increased to their highest levels. High predawn antheraxanthin and zeaxanthin contents were observed in the severe and very severe drought periods. Superoxide dismutase maintained high and fairly constant activity (1500–1800 U mg\u003Cjats:sup>−1\u003C\u002Fjats:sup> protein) and predawn maximum photochemistry efficiency of PSII was always above 0.8 throughout the whole study period. These results indicated that the photosynthetic apparatus of the oak leaves was highly capable of maintaining its function under the multiple stresses in different seasons in the present valley‐savanna.\u003C\u002Fjats:p>",{"EN":3216},"Photosynthesis, non‐photochemical pathways and activities of antioxidant enzymes in a resilient evergreen oak under different climatic conditions from a valley‐savanna in Southwest China",{"VOID":3218},"19121100",{"VOID":3220},"10.1111\u002Fj.1399-3054.2008.01171.x","Author affiliation is blank",[266],"https:\u002F\u002Fonlinelibrary.wiley.com\u002Fdoi\u002F10.1111\u002Fj.1399-3054.2008.01171.x",[3225,3236,3247,3258],{"id":3226,"sortIndex":151,"researcher":24,"roles":3227,"affiliations":3228,"properties":3229},"71b8d5fe-1410-44d6-ab7d-198b84a2d55d",[],[],{"openalex":3230,"orcid":3232,"title":3234},{"VOID":3231},"A5100778696",{"VOID":3233},"https:\u002F\u002Forcid.org\u002F0000-0002-6413-6703",{"EN":3235},"Hongcheng 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