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以采集后适应培养0~24 h以及添加甲烷和硫化钠培养24~240 h的南海冷泉区深海贻贝(Bathymodiolus platifrons)为材料,取其鳃部,分析附生菌的多样性与适应性变化状况。共分离鉴定出贻贝附生菌270株,对菌株的16S r DNA进行聚类分析,结果表明所分离菌株主要分布在4个门,21个属,其中变形菌的数量最多且多样性高。分析发现原位新采集的贻贝鳃部附生菌的多样性较高,6 h后附生菌的多样性明显降低。分别添加甲烷和硫化钠对深海贻贝进行培养,甲烷组与碳代谢有关的假单胞菌的数量逐渐增多,且在甲烷组240 h中发现2株食烷菌属菌株。硫化钠组的芽孢杆菌属所占比例升高。此外还发现4株潜在的新种。本研究实现了深海冷泉区贻贝的实验室培养,并对贻贝鳃部附生菌群结构进行了分析,丰富了海洋极端环境微生物资源库,并为深入解析贻贝与其附生菌之间的相互作用关系奠定了基础。 相似文献
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Lipolytic enzymes, including esterases and lipases, represent a group of hydrolases that catalyze the cleavage and formation of ester bonds. A novel esterase gene, scsEst01, was cloned from a South China Sea sediment metagenome. The scsEst01 gene consisted of 921 bp encoding 307 amino acid residues. The predicted amino acid sequence shared less than 90% identity with other lipolytic enzymes in the NCBI nonredundant protein database. Scs Est01 was successfully co-expressed in E scherichia coli BL21(DE3) with chaperones(dnaK-dna J-grp E) to prevent the formation of inclusion bodies. The recombinant protein was purified on an immobilized metal ion affinity column containing chelating Sepharose charged with Ni2 +. The enzyme was characterized using p-nitrophenol butyrate as a substrate. Scs Est01 had the highest lipolytic activity at 35℃ and p H 8.0, indicative of a meso-thermophilic alkaline esterase. Scs Est01 was thermostable at 20℃. The lipolytic activity of scs Est01 was strongly increased by Fe2 +, Mn 2+ and 1% Tween 80 or Tween 20. 相似文献
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