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荧光假单胞菌IP01中异丙苯降解基因的分析

Analysis of cumene (isopropylbenzene) degradation genes from Pseudomonas fluorescens IP01.

作者信息

Habe H, Kasuga K, Nojiri H, Yamane H, Omori T

机构信息

Biotechnology Research Center, University of Tokyo, Japan.

出版信息

Appl Environ Microbiol. 1996 Dec;62(12):4471-7. doi: 10.1128/aem.62.12.4471-4477.1996.

Abstract

We obtained the DNA fragments encoding 2-hydroxy-6-oxo-7-methylocta-2,4-dienoic acid (HOMODA) hydrolase in the cumene (isopropylbenzene) degrader Pseudomonas fluorescens strain IP01 via PCR using two synthesized oligonucleotides corresponding to the conserved regions within known meta-cleavage compound hydrolases. Following colony hybridization using the amplified DNA as a probe, a 4.5-kb HindIII fragment was isolated from P. fluorescens IP01. After determining the nucleotide sequence of this fragment, three open reading frames (ORF11 [cumH], ORF12 [cumD], and ORF13) were identified. The deduced amino acid sequence of ORF12 showed homology with meta-cleavage compound hydrolases encoded by the tod, dmp, xyl, and bph operons. Although the product of ORF12 was found to exhibit HOMODA and 2-hydroxy-6-oxohepta-2,4-dienoic acid (HOHDA) hydrolase activities, it did not exhibit 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid (HOPDA) hydrolase activity. The deduced amino acid sequence of ORF11 showed 40.4% homology with the sequence of todX in Pseudomonas putida F1 (Y. Wang, M. Ralings, D. T. Gibson, D. Labbé, H. Bergeron, R. Brousseau, and P. C. K. Lau, Mol. Gen. Genet. 246:570-579, 1995). The nucleotide sequence of ORF13 and its flanking region showed strong homology (91.0%) with IS52 from Pseudomonas savastanoi (Y. Yamada, P.-D. Lee, and T. Kosuge, Proc. Natl. Acad. Sci. USA 83:8263-8267, 1982). By characterization of cumH and cumD, the entire cum gene cluster from the cumene-degrader P. fluorescens IP01 (cumA1A2A3A4BCEGFHD) has been identified.

摘要

我们使用与已知间位裂解化合物水解酶保守区域相对应的两条合成寡核苷酸,通过聚合酶链反应(PCR)从异丙苯降解菌荧光假单胞菌IP01菌株中获得了编码2-羟基-6-氧代-7-甲基辛-2,4-二烯酸(HOMODA)水解酶的DNA片段。以扩增的DNA为探针进行菌落杂交后,从荧光假单胞菌IP01中分离出一个4.5kb的HindIII片段。在确定该片段的核苷酸序列后,鉴定出三个开放阅读框(ORF11 [cumH]、ORF12 [cumD]和ORF13)。ORF12推导的氨基酸序列与由tod、dmp、xyl和bph操纵子编码的间位裂解化合物水解酶具有同源性。虽然发现ORF12的产物具有HOMODA和2-羟基-6-氧代庚-2,4-二烯酸(HOHDA)水解酶活性,但它不具有2-羟基-6-氧代-6-苯基己-2,4-二烯酸(HOPDA)水解酶活性。ORF11推导的氨基酸序列与恶臭假单胞菌F1中todX的序列具有40.4%的同源性(Y. Wang、M. Ralings、D. T. Gibson、D. Labbé、H. Bergeron、R. Brousseau和P. C. K. Lau,《分子遗传学与普通遗传学》246:570-579,1995)。ORF13及其侧翼区域的核苷酸序列与番茄溃疡病菌IS52具有很强的同源性(91.0%)(Y. Yamada、P.-D. Lee和T. Kosuge,《美国国家科学院院刊》83:8263-8267,1982)。通过对cumH和cumD的表征,已鉴定出异丙苯降解菌荧光假单胞菌IP01完整的cum基因簇(cumA1A2A3A4BCEGFHD)。

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