A Novel Esterase from a Marine Metagenomic Library Exhibiting Salt Tolerance Ability

被引:27
作者
Fang, Zeming [1 ,2 ]
Li, Jingjing [1 ,2 ]
Wang, Quan [1 ,2 ]
Fang, Wei [1 ,2 ]
Peng, Hui [1 ,2 ]
Zhang, Xuecheng [1 ,2 ]
Xiao, Yazhong [1 ,2 ]
机构
[1] Anhui Univ, Sch Life Sci, Hefei 230601, Anhui, Peoples R China
[2] Anhui Prov Engn Technol Res Ctr Microorganisms &, Hefei 230601, Anhui, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Esterase; marine metagenome; salt tolerance; BIOTECHNOLOGICAL APPLICATIONS; LIPASE; IDENTIFICATION; EXPRESSION; ENZYMES; CLONING; GENE; CLASSIFICATION; BIOCATALYSTS; SEDIMENTS;
D O I
10.4014/jmb.1311.11071
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A putative lipolytic enzyme gene, named as est9x, was obtained from a marine microbial metagenome of the South China Sea. Sequence analysis showed that Est9X shares lower than 27% sequence identities with the characterized lipolytic enzymes, but possesses a catalytic triad highly conserved in lipolytic enzymes of the alpha/beta hydrolase superfamily. By phylogenetic tree construction, Est9X was grouped into a new lipase/esterase family. To understand Est9X protein in depth, it was recombinantly expressed, purified, and biochemically characterized. Within potential hydrolytic activities, only lipase/esterase activity was detected for Est9X, confirming its identity as a lipolytic enzyme. When using p-nitrophenol esters with varying lengths of fatty acid as substrates, Est9X exhibited the highest activity to the C2 substrate, indicating it is an esterase. The optimal activity of Est9X occurred at a temperature of 65 degrees C, and Est9X was pretty stable below the optimum temperature. Distinguished from other salt-tolerant esterases, Est9X's activity was tolerant to and even promoted by as high as 4 M NaCl. Our results imply that Est9X is a unique esterase and could be a potential candidate for industrial application under extreme conditions.
引用
收藏
页码:771 / 780
页数:10
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