首页> 外文期刊>International Biodeterioration & Biodegradation >Isolation and characterization of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) degrading bacteria and purification of PHBV depolymerase from newly isolated Bacillus sp. AF3
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Isolation and characterization of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) degrading bacteria and purification of PHBV depolymerase from newly isolated Bacillus sp. AF3

机译:聚(3-羟基丁酸酯-co-3-羟基戊酸酯)降解细菌的分离和鉴定以及从新分离的芽孢杆菌中纯化PHBV解聚酶。 AF3

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摘要

The contribution of bacteria, isolated from sewage sludge, towards the microbial degradation of poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) was studied. A microbial consortium was inoculated on mineral salt agar plates containing different concentrations of PHBV as a substrate. The PHBV degraders showed optimum depolymerase production at pH 7.0, 37DGC, and 0.4% substrate concentration during 2-5 weeks of incubation. Additional carbon sources like glucose, fructose, sucrose, lactose and nitrogen sources including yeast extract were used as co-metabolites. The highest degree of degradation of PHBV was observed in the presence of glucose. Among the surfactants, Tween 80, was found to be a good inducer for the release of extracellular depolymerase enzyme as compared to Tween 20. When the PHBV depolymerase activity of isolates present in the consortium was determined separately, it was found that the enzyme activity was higher in case of Bacillus sp. AF3. The purification steps included ammonium sulfate fractionation and gel permeation chromatography on Sephadex G-75. The enzyme has been purified to homogeneity as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and molecular weight was found to be approximately 37kDa.
机译:研究了从污水污泥中分离出来的细菌对聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV)微生物降解的贡献。将微生物财团接种在含有不同浓度的PHBV作为底物的无机盐琼脂平板上。在温育2-5周期间,PHBV降解剂在pH 7.0、37DGC和0.4%底物浓度下显示最佳解聚酶产生。其他碳源(如葡萄糖,果糖,蔗糖,乳糖和氮源,包括酵母提取物)被用作共代谢物。在葡萄糖存在下观察到最高的PHBV降解程度。在表面活性剂中,与Tween 20相比,发现Tween 80是释放细胞外解聚酶的良好诱导剂。当单独测定财团中存在的分离物的PHBV解聚酶活性时,发现该酶活性为。如果是芽孢杆菌,则更高。 AF3。纯化步骤包括硫酸铵分级分离和在Sephadex G-75上的凝胶渗透色谱。经十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)判断,该酶已纯化至均一,分子量约为37kDa。

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