The catabolism of 2,4-xylenol and p-cresol share the enzymes for the oxidation of para-methyl group in Pseudomonas putida NCIMB 9866

被引:103
作者
Chen, Yan-Fei [1 ,2 ]
Chao, Hongjun [1 ,2 ]
Zhou, Ning-Yi [1 ]
机构
[1] Chinese Acad Sci, Wuhan Inst Virol, Key Lab Agr & Environm Microbiol, Wuhan 430071, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
2,4-Xylenol; Catabolism; p-Cresol; Pseudomonas putida NCIMB 9866; BENZALDEHYDE DEHYDROGENASE; SUBSTRATE SPECIFICITIES; EXPRESSION; PLASMID; GENES; METHYLHYDROXYLASE; CLONING; FLAVOCYTOCHROME; IDENTIFICATION; PURIFICATION;
D O I
10.1007/s00253-013-5001-z
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
Pseudomonas putida NCIMB 9866 utilizes p-cresol or 2,4-xylenol as a sole carbon and energy source. Enzymes catalyzing the oxidation of the para-methyl group of p-cresol have been studied in detail. However, those responsible for the oxidation of the para-methyl group in 2,4-xylenol catabolism are still not reported. In this study, real-time quantitative PCR analysis indicated pchC- and pchF-encoded p-cresol methylhydroxylase (PCMH) and pchA-encoded p-hydroxybenzaldehyde dehydrogenase (PHBDD) in p-cresol catabolism were also likely involved in the catabolism of 2,4-xylenol. Enzyme activity assays and intermediate identification indicated that the PCMH and PHBDD catalyzed the oxidations of 2,4-xylenol to 4-hydroxy-3-methylbenzaldehyde and 4-hydroxy-3-methylbenzaldehyde to 4-hydroxy-3-methylbenzoic acid, respectively. Furthermore, the PCMH-encoding gene pchF was found to be necessary for the catabolism of 2,4-xylenol, whereas the PHBDD-encoding gene pchA was not essential for the catabolism by gene knockout and complementation. Analyses of the maximum specific growth rate (mu (m)) and specific activity of the gene-knockout strain to different intermediates revealed the presence of other enzyme(s) with PHBDD activity in strain 9866. However, PHBDD played a major role in the catabolism of 2,4-xylenol in contrast to the other enzyme(s).
引用
收藏
页码:1349 / 1356
页数:8
相关论文
共 23 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   BACTERIAL METABOLISM OF 2,4-XYLENOL [J].
CHAPMAN, PJ ;
HOPPER, DJ .
BIOCHEMICAL JOURNAL, 1968, 110 (03) :491-&
[3]   Organization and sequences of p-hydroxybenzaldehyde dehydrogenase and other plasmid-encoded genes for early enzymes of the p-cresol degradative pathway in Pseudomonas putida NCIMB 9866 and 9869 [J].
Cronin, CN ;
Kim, J ;
Fuller, JH ;
Zhang, XP ;
McIntire, WS .
DNA SEQUENCE, 1999, 10 (01) :7-17
[4]   pUCP-Nco and pUCP-Nde:: Escherichia-Pseudomonas shuttle vectors for recombinant protein expression in Pseudomonas [J].
Cronin, CN ;
McIntire, WS .
ANALYTICAL BIOCHEMISTRY, 1999, 272 (01) :112-115
[5]  
DEAN HF, 1989, FEMS MICROBIOL LETT, V61, P153, DOI 10.1016/0378-1097(89)90188-2
[6]   Maintenance of broad-host-range incompatibility group P and group Q plasmids and transposition of Tn5 in Bartonella henselae following conjugal plasmid transfer from Escherichia coli [J].
Dehio, C ;
Meyer, M .
JOURNAL OF BACTERIOLOGY, 1997, 179 (02) :538-540
[7]  
Dennis JJ, 1998, APPL ENVIRON MICROB, V64, P2710
[8]  
ELMANSI EMT, 1990, FEMS MICROBIOL LETT, V66, P147, DOI 10.1111/j.1574-6968.1990.tb03987.x
[9]   PURIFICATION AND PROPERTIES OF 4-HYDROXYISOPHTHALATE HYDROXYLASE FROM PSEUDOMONAS-PUTIDA NCIB-9866 [J].
ELMORSI, EA ;
HOPPER, DJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1977, 76 (01) :197-208
[10]   A broad-host-range Flp-FRT recombination system for site-specific excision of chromosomally-located DNA sequences:: application for isolation of unmarked Pseudomonas aeruginosa mutants [J].
Hoang, TT ;
Karkhoff-Schweizer, RR ;
Kutchma, AJ ;
Schweizer, HP .
GENE, 1998, 212 (01) :77-86