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铜绿假单胞菌142编码卤代苯甲酸氧解邻位脱卤的ohb基因的克隆、表达及核苷酸序列

Cloning, expression, and nucleotide sequence of the Pseudomonas aeruginosa 142 ohb genes coding for oxygenolytic ortho dehalogenation of halobenzoates.

作者信息

Tsoi T V, Plotnikova E G, Cole J R, Guerin W F, Bagdasarian M, Tiedje J M

机构信息

Center for Microbial Ecology, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

Appl Environ Microbiol. 1999 May;65(5):2151-62. doi: 10.1128/AEM.65.5.2151-2162.1999.

Abstract

We have cloned and characterized novel oxygenolytic ortho-dehalogenation (ohb) genes from 2-chlorobenzoate (2-CBA)- and 2,4-dichlorobenzoate (2,4-dCBA)-degrading Pseudomonas aeruginosa 142. Among 3,700 Escherichia coli recombinants, two clones, DH5alphaF'(pOD22) and DH5alphaF'(pOD33), converted 2-CBA to catechol and 2,4-dCBA and 2,5-dCBA to 4-chlorocatechol. A subclone of pOD33, plasmid pE43, containing the 3,687-bp minimized ohb DNA region conferred to P. putida PB2440 the ability to grow on 2-CBA as a sole carbon source. Strain PB2440(pE43) also oxidized but did not grow on 2,4-dCBA, 2,5-dCBA, or 2,6-dCBA. Terminal oxidoreductase ISPOHB structural genes ohbA and ohbB, which encode polypeptides with molecular masses of 20,253 Da (beta-ISP) and 48,243 Da (alpha-ISP), respectively, were identified; these proteins are in accord with the 22- and 48-kDa (as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis) polypeptides synthesized in E. coli and P. aeruginosa parental strain 142. The ortho-halobenzoate 1,2-dioxygenase activity was manifested in the absence of ferredoxin and reductase genes, suggesting that the ISPOHB utilized electron transfer components provided by the heterologous hosts. ISPOHB formed a new phylogenetic cluster that includes aromatic oxygenases featuring atypical structural-functional organization and is distant from the other members of the family of primary aromatic oxygenases. A putative IclR-type regulatory gene (ohbR) was located upstream of the ohbAB genes. An open reading frame (ohbC) of unknown function that overlaps lengthwise with ohbB but is transcribed in the opposite direction was found. The ohbC gene codes for a 48,969-Da polypeptide, in accord with the 49-kDa protein detected in E. coli. The ohb genes are flanked by an IS1396-like sequence containing a putative gene for a 39,715-Da transposase A (tnpA) at positions 4731 to 5747 and a putative gene for a 45,247-Da DNA topoisomerase I/III (top) at positions 346 to 1563. The ohb DNA region is bordered by 14-bp imperfect inverted repeats at positions 56 to 69 and 5984 to 5997.

摘要

我们从降解2-氯苯甲酸(2-CBA)和2,4-二氯苯甲酸(2,4-dCBA)的铜绿假单胞菌142中克隆并鉴定了新型氧解邻位脱卤(ohb)基因。在3700个大肠杆菌重组体中,两个克隆,DH5alphaF'(pOD22) 和DH5alphaF'(pOD33),将2-CBA转化为儿茶酚,将2,4-dCBA和2,5-dCBA转化为4-氯儿茶酚。pOD33的一个亚克隆,质粒pE43,包含3687 bp的最小化ohb DNA区域,赋予恶臭假单胞菌PB2440以2-CBA作为唯一碳源生长的能力。菌株PB2440(pE43) 也能氧化2,4-dCBA、2,5-dCBA或2,6-dCBA,但不能在其上生长。鉴定出末端氧化还原酶ISPOHB结构基因ohbA和ohbB,它们分别编码分子量为20253 Da(β-ISP)和48243 Da(α-ISP)的多肽;这些蛋白质与在大肠杆菌和铜绿假单胞菌亲本菌株142中合成的22 kDa和48 kDa(通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定)多肽一致。邻卤苯甲酸1,2-双加氧酶活性在没有铁氧化还原蛋白和还原酶基因的情况下表现出来,这表明ISPOHB利用了异源宿主提供的电子传递成分。ISPOHB形成了一个新的系统发育簇,其中包括具有非典型结构-功能组织的芳香加氧酶,并且与初级芳香加氧酶家族的其他成员相距较远。一个假定的IclR型调节基因(ohbR)位于ohbAB基因的上游。发现了一个功能未知的开放阅读框(ohbC),它与ohbB在长度上重叠,但转录方向相反。ohbC基因编码一种48969 Da的多肽,与在大肠杆菌中检测到的49 kDa蛋白质一致。ohb基因两侧是一个IS1396样序列,在4731至5747位含有一个假定的39715 Da转座酶A(tnpA)基因,在346至1563位含有一个假定的45247 Da DNA拓扑异构酶I/III(top)基因。ohb DNA区域在56至69位和5984至5997位由14 bp的不完全反向重复序列界定。

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