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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

邮发代号 80-973

2018 Impact Factor: 3.883

Frontiers of Environmental Science & Engineering  2014, Vol. 8 Issue (4): 539-546   https://doi.org/10.1007/s11783-013-0616-y
  本期目录
Multistep conversion of cresols by phenol hydroxylase and 2,3-dihydroxy-biphenyl 1,2-dioxygenase
Shengnan SHI1,Fang MA1,*(),Tieheng SUN1,Ang LI1,Jiti ZHOU2,Yuanyuan QU2,*()
1. State Key Laboratory of Urban Water Resource and Environment, School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090, China
2. Key Laboratory of Industrial Ecology and Environmental Engineering (Ministry of Education), School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024, China
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Abstract

A multistep conversion system composed of phenol hydroxylase (PHIND) and 2,3-dihydroxy-biphenyl 1,2-dioxygenase (BphCLA-4) was used to synthesize methylcatechols and semialdehydes from o- and m-cresol for the first time. Docking studies displayed by PyMOL predicted that cresols and methylcatechols could be theoretically transformed by this multistep conversion system. High performance liquid chromatography mass spectrometry (HPLC-MS) analysis also indicated that the products formed from multistep conversion were the corresponding 3-methylcatechol, 4-methylcatechol, 2-hydroxy-3-methyl-6-oxohexa-2,4-dienoic acid (2-hydroxy-3-methyl-ODA) and 2-hydroxy-5-methyl-6-oxohexa-2,4-dienoic acid (2-hydroxy-5-methyl-ODA). The optimal cell concentrations of the recombinant E. coli strain BL21 (DE3) expressing phenol hydroxylase (PHIND) and 2,3-dihydroxy-biphenyl 1,2-dioxygenase (BphCLA-4) and pH for the multistep conversion of o- and m-cresol were 4.0 (g·L-1 cell dry weight) and pH 8.0, respectively. For the first step conversion, the formation rate of 3-methylcatechol (0.29 μmol·L-1·min-1·mg-1 cell dry weight) from o-cresol was similarly with that of methylcatechols (0.28 μmol·L-1·min-1·mg-1 cell dry weight) from m-cresol by strain PHIND. For the second step conversion, strain BphCLA-4 showed higher formation rate (0.83 μmol·L-1·min-1·mg-1 cell dry weight) for 2-hydroxy-3-methyl-ODA and 2-hydroxy-5-methyl-ODA from m-cresol, which was 1.1-fold higher than that for 2-hydroxy-3-methyl-ODA (0.77 μmol·L-1·min-1·mg-1cell dry weight) from o-cresol. The present study suggested the potential application of the multistep conversion system for the production of chemical synthons and high-value products.

Key wordsmultistep conversion    cresols    phenol hydroxylase    2    3-dihydroxybiphenyl 1    2-dioxygenase    methylcatechols
收稿日期: 2012-12-29      出版日期: 2014-06-11
Corresponding Author(s): Fang MA   
 引用本文:   
. [J]. Frontiers of Environmental Science & Engineering, 2014, 8(4): 539-546.
Shengnan SHI,Fang MA,Tieheng SUN,Ang LI,Jiti ZHOU,Yuanyuan QU. Multistep conversion of cresols by phenol hydroxylase and 2,3-dihydroxy-biphenyl 1,2-dioxygenase. Front.Environ.Sci.Eng., 2014, 8(4): 539-546.
 链接本文:  
https://academic.hep.com.cn/fese/CN/10.1007/s11783-013-0616-y
https://academic.hep.com.cn/fese/CN/Y2014/V8/I4/539
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