Catalytic transformation of HODAs using an efficient meta-cleavage product hydrolase-spore surface display system

被引:10
|
作者
Qu, Yuanyuan [1 ]
Wang, Jingwei [1 ]
Zhang, Zhaojing [1 ]
Shi, Shengnan [2 ]
Li, Duanxing [1 ]
Shen, Wenli [1 ]
Shen, E. [1 ]
Zhou, Jiti [1 ]
机构
[1] Dalian Univ Technol, Sch Environm Sci & Technol, Key Lab Ind Ecol & Environm Engn, Minist Educ, Dalian 116024, Peoples R China
[2] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
基金
中国国家自然科学基金;
关键词
Surface display system; meta-Cleavage product hydrolase; 2-Hydroxy-6-oxohexa-2,4-dienoic acid; (HODA); Catalytic transformation; ICE-NUCLEATION PROTEIN; D-NEURAMINIC ACID; BACILLUS-SUBTILIS; POLYCHLORINATED-BIPHENYLS; CELL-SURFACE; MICROBIAL-DEGRADATION; ESCHERICHIA-COLI; SERINE HYDROLASE; RESISTANCE; CONVERSION;
D O I
10.1016/j.molcatb.2014.02.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The accumulation of 2-hydroxy-6-oxohexa-2,4-dienoic acids (HODAs) in the process of aromatics transformation will hinder the mineralization rate. In this study, a novel type of biocatalyst, meta-cleavage product (MCP) hydrolase (MfphA and BphD) displayed on the surface of Bacillus subtilis 168 spores, was developed for the transformation of HODAs. The successful display of CotG-MfphA and CotG-BphD fusion protein on the surface of spore were confirmed by western blot analysis and activity measurement. The optimal transformation conditions by spore surface-displayed MfphA and BphD were found to be 70 C and pH 7. The thermal and pH stability analysis exhibited that spore surface-displayed MfphA and BphD were stable and retained more than 80% of relative activities even at 80 degrees C and pH 10. Meanwhile, recycling experiments showed that the conversion percentage of HODA by surface-displayed MfphA and BphD were not significantly decreased throughout the reutilization process, which still retained 45% and 70% at the tenth cycle, respectively. To the best of our knowledge, this is the first report concerning the B. subtilis 168 spore surface-displayed MCP hydrolases. The high activities and good recycle performance suggested that this novel biocatalyst system could serve as a suitable alternative for HODAs transformation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:204 / 210
页数:7
相关论文
共 5 条
  • [1] Insight into the catalytic mechanism of meta-cleavage product hydrolase BphD: a quantum mechanics/molecular mechanics study
    Li, Yanwei
    Zhang, Ruiming
    Du, Likai
    Zhang, Qingzhu
    Wang, Wenxing
    RSC ADVANCES, 2015, 5 (82) : 66591 - 66597
  • [2] Identification of an Acyl-Enzyme Intermediate in a meta-Cleavage Product Hydrolase Reveals the Versatility of the Catalytic Triad
    Ruzzini, Antonio C.
    Ghosh, Subhangi
    Horsman, Geoff P.
    Foster, Leonard J.
    Bolin, Jeffrey T.
    Eltis, Lindsay D.
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (10) : 4615 - 4624
  • [3] Improving the catalytic efficiency of a meta-cleavage product hydrolase (CumD) from Pseudomonas fluorescens IPO1
    Jun, So-Young
    Fushinobu, Shinya
    Nojiri, Hideaki
    Omori, Toshio
    Shoun, Hirofumi
    Wakagi, Takayoshi
    BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2006, 1764 (07): : 1159 - 1166
  • [4] The key role of a non-active-site residue Met148 on the catalytic efficiency of meta-cleavage product hydrolase BphD
    Zhou, Hao
    Qu, Yuanyuan
    Kong, Chunlei
    Shen, E.
    Wang, Jingwei
    Zhang, Xuwang
    Ma, Qiao
    Zhou, Jiti
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2013, 97 (24) : 10399 - 10411
  • [5] The key role of a non-active-site residue Met148 on the catalytic efficiency of meta-cleavage product hydrolase BphD
    Hao Zhou
    Yuanyuan Qu
    Chunlei Kong
    E. Shen
    Jingwei Wang
    Xuwang Zhang
    Qiao Ma
    Jiti Zhou
    Applied Microbiology and Biotechnology, 2013, 97 : 10399 - 10411