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
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.
MüllerJ A, GalushkoA S, KapplerA, SchinkB. Anaerobic degradation of m-cresol by Desulfobacterium cetonicum is initiated by formation of 3-hydroxybenzylsuccinate. Archives of Microbiology, 1999, 172(5): 287-294 doi: 10.1007/s002030050782 pmid: 10550470
2
LondryK L, FedorakP M, SuflitaJ M. Anaerobic degradation of m-Cresol by a sulfate-reducing bacterium. Applied and Environmental Microbiology, 1997, 63(8): 3170-3175 pmid: 16535673
3
TallurP N, MegadiV B, KamanavalliC M, NinnekarH Z. Biodegradation of p-cresol by Bacillus sp. strain PHN 1. Current Microbiology, 2006, 53(6): 529-533 doi: 10.1007/s00284-006-0309-x pmid: 17106800
4
KnackmussH J. Biochemistry and practical implications of organohalide degradation. In: KlugM J, ReddyC A, eds. Current Perspectives in Microbial. Washington, D C: American Society for Microbiology, 1984, 687-693
5
DagleyS, GibsonD T. The bacterial degradation of catechol. The Biochemical Journal, 1965, 95(2): 466-474 pmid: 14340096
6
CoulombelL, NolanL C, NikodinovicJ, DoyleE M, O’ConnorK E. Biotransformation of 4-halophenols to 4-halocatechols using Escherichia coli expressing 4-hydroxyphenylacetate 3-hydroxylase. Applied Microbiology and Biotechnology, 2011, 89(6): 1867-1875 doi: 10.1007/s00253-010-2969-5 pmid: 21057945
7
QuY Y, ShiS N, QiaoM, KongC L, ZhouH, ZhangX W, ZhouJ T. Multistep conversion of para-substituted phenols by phenol hydroxylase and 2,3-dihydroxy-biphenyl 1,2-dioxygenase. Applied Biochemistry and Biotechnology, 2013, 169(7): 2064-2075. doi: 10.1007/s12010-013-0112-7 pmid: 19140028
8
TaoY, FishmanA, BentleyW E, WoodT K. Oxidation of benzene to phenol, catechol, and 1,2,3-trihydroxybenzene by toluene 4-monooxygenase of Pseudomonas mendocina KR1 and toluene 3-monooxygenase of Ralstonia pickettii PKO1. Applied and Environmental Microbiology, 2004, 70(7): 3814-3820 doi: 10.1128/AEM.70.7.3814-3820.2004 pmid: 15240250
9
RobertsS J, MorrisJ C, DobsonR C J, GerrardJ A. The preparation of (S)-aspartate semi-aldehyde appropriate for use in biochemical studies. Bioorganic & Medicinal Chemistry Letters, 2003, 13(2): 265-267 doi: 10.1016/S0960-894X(02)00923-X pmid: 12482436
10
ParalesR E, BruceN C, SchmidA, WackettL P. Biodegradation, biotransformation, and biocatalysis (b3). Applied and Environmental Microbiology, 2002, 68(10): 4699-4709 doi: 10.1128/AEM.68.10.4699-4709.2002 pmid: 12324310
11
GarikipatiS V, McIverA M, PeeplesT L. Whole-cell biocatalysis for 1-naphthol production in liquid-liquid biphasic systems. Applied and Environmental Microbiology, 2009, 75(20): 6545-6552 doi: 10.1128/AEM.00434-09 pmid: 19700554
12
PollardD J, WoodleyJ M. Biocatalysis for pharmaceutical intermediates: the future is now. Trends in Biotechnology, 2007, 25(2): 66-73 doi: 10.1016/j.tibtech.2006.12.005 pmid: 17184862
AzeradR. Editorial overview: better enzyme for green chemistry. Current Opinion in Biotechnology, 2001, 12(6): 533-534 doi: 10.1016/S0958-1669(01)00259-2
15
StraathofA J J, PankeS, SchmidA. The production of fine chemicals by biotransformations. Current Opinion in Biotechnology, 2002, 13(6): 548-556 doi: 10.1016/S0958-1669(02)00360-9 pmid: 12482513
16
SelinheimoE, GasparettiC, MattinenM L, SteffensenC L, BuchertJ, KruusK. Comparison of substrate specificity of tyrosinases from Trichoderma reesei and Agaricus bisporus. Enzyme and Microbial Technology, 2009, 44(1): 1-10 doi: 10.1016/j.enzmictec.2008.09.013
17
SazinskyM H, DuntenP W, McCormickM S, DiDonatoA, LippardS J. X-ray structure of a hydroxylase-regulatory protein complex from a hydrocarbon-oxidizing multicomponent monooxygenase, Pseudomonas sp. OX1 phenol hydroxylase. Biochemistry, 2006, 45(51): 15392-15404 doi: 10.1021/bi0618969 pmid: 17176061
18
EltisL D, HofmannB, HechtH J, LünsdorfH, TimmisK N. Purification and crystallization of 2,3-dihydroxybiphenyl 1,2-dioxygenase. The Journal of Biological Chemistry, 1993, 268(4): 2727-2732 pmid: 8428946
19
WuZ L, PodustL M, GuengerichF P. Expansion of substrate specificity of cytochrome P450 2A6 by random and site-directed mutagenesis. The Journal of Biological Chemistry, 2005, 280(49): 41090-41100 doi: 10.1074/jbc.M508182200 pmid: 16215230
20
MorrisG M, Lim-WilbyM. Molecular docking. Methods in Molecular Biology (Clifton, N.J.), 2008, 443(1064-3745): 365-382 doi: 10.1007/978-1-59745-177-2_19 pmid: 18446297
21
MaF, ShiS N, SunT H, LiA, ZhouJ T, QuY Y. Biotransformation of benzene and toluene to catechols by phenol hydroxylase from Arthrobacter sp. W1. Applied Microbiology and Biotechnology, 2013, 97(11): 5097-5103 doi: 10.1007/s00253-012-4301-z pmid: 22854893
22
CarliellC M, BarclayS J, NaidooN, BuckleyC A, MulhollandD A, SeniorE. Microbial decolorization of a reactive azo dye under anaerobic conditions. Water SA, 1995, 21(1): 61-69