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
[12]   PURIFICATION AND PROPERTIES OF PARA-CRESOL-(ACCEPTOR) OXIDOREDUCTASE (HYDROXYLATING), A FLAVOCYTOCHROME FROM PSEUDOMONAS-PUTIDA [J].
HOPPER, DJ ;
TAYLOR, DG .
BIOCHEMICAL JOURNAL, 1977, 167 (01) :155-162
[13]   OVERLAPPING SUBSTRATE SPECIFICITIES OF BENZALDEHYDE DEHYDROGENASE (THE XYLC GENE-PRODUCT) AND 2-HYDROXYMUCONIC SEMIALDEHYDE DEHYDROGENASE (THE XYLG GENE-PRODUCT) ENCODED BY TOL PLASMID PWWO OF PSEUDOMONAS-PUTIDA [J].
INOUE, J ;
SHAW, JP ;
REKIK, M ;
HARAYAMA, S .
JOURNAL OF BACTERIOLOGY, 1995, 177 (05) :1196-1201
[14]   areABC genes determine the catabolism of aryl esters in Acinetobacter sp strain ADP1 [J].
Jones, RM ;
Collier, LS ;
Neidle, EL ;
Williams, PA .
JOURNAL OF BACTERIOLOGY, 1999, 181 (15) :4568-4575
[15]   IMPROVED BROAD-HOST-RANGE PLASMIDS FOR DNA CLONING IN GRAM-NEGATIVE BACTERIA [J].
KEEN, NT ;
TAMAKI, S ;
KOBAYASHI, D ;
TROLLINGER, D .
GENE, 1988, 70 (01) :191-197
[16]   CLONING, SEQUENCING, AND EXPRESSION OF THE STRUCTURAL GENES FOR THE CYTOCHROME AND FLAVOPROTEIN SUBUNITS OF P-CRESOL METHYLHYDROXYLASE FROM 2 STRAINS OF PSEUDOMONAS-PUTIDA [J].
KIM, JH ;
FULLER, JH ;
CECCHINI, G ;
MCINTIRE, WS .
JOURNAL OF BACTERIOLOGY, 1994, 176 (20) :6349-6361
[17]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[18]  
MACKINTOSH RW, 1988, BIOCHEM J, V255, P653
[19]   RESOLUTION OF PARA-CRESOL METHYLHYDROXYLASE INTO CATALYTICALLY ACTIVE SUBUNITS AND RECONSTITUTION OF THE FLAVOCYTOCHROME [J].
MCINTIRE, W ;
SINGER, TP .
FEBS LETTERS, 1982, 143 (02) :316-318
[20]   ANAEROBIC DEGRADATION OF CRESOLS BY DENITRIFYING BACTERIA [J].
RUDOLPHI, A ;
TSCHECH, A ;
FUCHS, G .
ARCHIVES OF MICROBIOLOGY, 1991, 155 (03) :238-248