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Characterizing the new bacterial isolates of high yielding exopolysaccharides under hypersaline conditions

机译:在高盐条件下表征高产胞外多糖的新细菌分离株

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摘要

The ability of plant growth promoting bacteria (PGPR) to survive under salinity stress has important implications on the growth of their host plants. The production of different biochemicals by the bacteria including exopolysaccharides (EPS) may determine their survival as well as their alleviating effects under stress. However, one important approach, which deserves more attention, is the performance of PGPR under stressed conditions such as hypersaline conditions. Accordingly, the objectives of this study were: 1) the isolation and characterization of new bacterial isolates of high yielding EPS from a hypersaline soil, and 2) the investigation of EPS structure in the presence of salt. Samples of soil were spread on nutrient agar +/- %5 NaCl to determine the salt tolerant colonies with the maximum tolerable salt concentrations (MTC). Among the isolates of "salt tolerant bacteria" (STB), six isolates had the potential to produce EPS. According to 16S rDNA gene sequencing, three salt tolerant EPS-producing isolates were identified as Bacillus aerius ATHM35, Arthrobacter luteolus ATHM 36, and Halomonas eurihalina ATHM 37. It is the first time that Bacillus aerius and Arthrobacter luteolus have been isolated from hypersaline soils. The biochemical analyses indicated that the isolates were able to produce a wide range of products including enzymes such as urease, lactose, oxidase and catalase. With increasing salt concentration the production of EPS by the isolates significantly (P 0.05) increased. H. eurihalina showed the MTC of 25% and produced the highest amounts of EPS (0.277 gL(-1)) significantly higher than the other isolates. The FTIR spectrum of EPSs showed they are heteropolysaccharides containing the functional groups of hydroxyl, alkyne, amides and carboxyl, and the absorption peaks related to sugar units. These new salt-tolerant isolates of high yielding EPS are suitable biotechnological candidates for agricultural and environmental applications. (C) 2018 Elsevier Ltd. All rights reserved.
机译:植物生长促进细菌(PGPR)在盐分胁迫下生存的能力对其寄主植物的生长具有重要意义。细菌产生的不同生物化学物质包括胞外多糖(EPS)可能决定其生存力以及在压力下的缓解作用。但是,一种值得更多关注的重要方法是PGPR在压力条件下(例如高盐条件)的性能。因此,本研究的目标是:1)从高盐分土壤中分离和鉴定高产EPS的新型细菌分离株,以及2)在盐存在下研究EPS结构。将土壤样品铺在营养琼脂+/-%5 NaCl上,以确定具有最大耐盐浓度(MTC)的耐盐菌落。在“耐盐细菌”(STB)的分离物中,有六个分离物具有产生EPS的潜力。根据16S rDNA基因测序,鉴定出三种耐盐的EPS产生菌,分别为铜绿芽孢杆菌ATHM35,黄杆菌节杆菌ATHM 36和盐藻嗜盐杆菌ATHM37。这是首次从高盐渍土中分离出铜绿芽孢杆菌和黄杆菌。生化分析表明,分离物能够产生多种产物,包括诸如脲酶,乳糖,氧化酶和过氧化氢酶的酶。随着盐浓度的增加,分离物的EPS产量显着增加(P <0.05)。 H. eurihalina显示MTC为25%,并产生最高数量的EPS(0.277 gL(-1)),明显高于其他分离株。 EPS的FTIR光谱表明它们是含有羟基,炔烃,酰胺和羧基官能团的杂多糖,其吸收峰与糖单元有关。这些新的高产EPS耐盐分离株是适合农业和环境应用的生物技术候选物。 (C)2018 Elsevier Ltd.保留所有权利。

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