首页> 外文OA文献 >Two Novel Alkane Hydroxylase-Rubredoxin Fusion Genes Isolated from a Dietzia Bacterium and the Functions of Fused Rubredoxin Domains in Long-Chain n-Alkane Degradation▿
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Two Novel Alkane Hydroxylase-Rubredoxin Fusion Genes Isolated from a Dietzia Bacterium and the Functions of Fused Rubredoxin Domains in Long-Chain n-Alkane Degradation▿

机译:拟南芥细菌中分离出的两个新的烷烃羟化酶-Rubredoxin融合基因及其融合的rubredoxin域在长链正构烷烃降解中的功能▿

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摘要

Two alkane hydroxylase-rubredoxin fusion gene homologs (alkW1 and alkW2) were cloned from a Dietzia strain, designated DQ12-45-1b, which can grow on crude oil and n-alkanes ranging in length from 6 to 40 carbon atoms as sole carbon sources. Both AlkW1 and AlkW2 have an integral-membrane alkane monooxygenase (AlkB) conserved domain and a rubredoxin (Rd) conserved domain which are fused together. Phylogenetic analysis showed that these two AlkB-fused Rd domains formed a novel third cluster with all the Rds from the alkane hydroxylase-rubredoxin fusion gene clusters in Gram-positive bacteria and that this third cluster was distant from the known AlkG1- and AlkG2-type Rds. Expression of the alkW1 gene in DQ12-45-1b was induced when cells were grown on C8 to C32 n-alkanes as sole carbon sources, but expression of the alkW2 gene was not detected. Functional heterologous expression in an alkB deletion mutant of Pseudomonas fluorescens KOB2Δ1 suggested the alkW1 could restore the growth of KOB2Δ1 on C14 and C16 n-alkanes and induce faster growth on C18 to C32 n-alkanes than alkW1ΔRd, the Rd domain deletion mutant gene of alkW1, which also caused faster growth than KOB2Δ1 itself. In addition, the artificial fusion of AlkB from the Gram-negative P. fluorescens CHA0 and the Rds from both Gram-negative P. fluorescens CHA0 and Gram-positive Dietzia sp. DQ12-45-1b significantly increased the degradation of C32 alkane compared to that seen with AlkB itself. In conclusion, the alkW1 gene cloned from Dietzia species encoded an alkane hydroxylase which increased growth on and degradation of n-alkanes up to C32 in length, with its fused rubredoxin domain being necessary to maintain the functions. In addition, the fusion of alkane hydroxylase and rubredoxin genes from both Gram-positive and -negative bacteria can increase the degradation of long-chain n-alkanes (such as C32) in the Gram-negative bacterium.
机译:从Dietzia菌株DQ12-45-1b中克隆了两个烷烃羟化酶-氧化还原酶融合基因同源物(alkW1和alkW2),它们可以在原油和长度为6至40个碳原子的正构烷烃上生长,作为唯一的碳源。 AlkW1和AlkW2都具有融合在一起的整体膜烷烃单加氧酶(AlkB)保守域和rubredoxin(Rd)保守域。系统发育分析表明,这两个AlkB融合的Rd结构域形成了一个新的第三簇,其中所有Rds来自革兰氏阳性细菌中的烷烃羟化酶-rubredoxin融合基因簇,并且该第三簇与已知的AlkG1和AlkG2型相距很远。路数当细胞作为唯一碳源在C8至C32正构烷烃上生长时,诱导了DQ12-45-1b中alkW1基因的表达,但未检测到alkW2基因的表达。在荧光假单胞菌KOB2Δ1的alkB缺失突变体中的功能异源表达表明,相比于alkW1的Rd域缺失突变基因alkW1ΔRd,alkW1可以恢复K14和C16正构烷烃上KOB2Δ1的生长,并诱导C18至C32正构烷烃的生长更快。 ,其生长速度也快于KOB2Δ1本身。另外,来自革兰氏阴性假单胞菌CHA0的AlkB和来自革兰氏阴性假单胞菌CHA0和革兰氏阳性的Dietzia sp。的Rds的人工融合。与AlkB本身相比,DQ12-45-1b显着增加了C32烷烃的降解。总之,从Dietzia物种克隆的alkW1基因编码了一种烷烃羟化酶,该酶可增加正链烷烃的生长和降解直至C32的长度,其融合的氧化还原蛋白结构域对于维持功能是必不可少的。此外,革兰氏阳性和阴性细菌中烷烃羟化酶和rubredoxin基因的融合可以增加革兰氏阴性细菌中长链正构烷烃(例如C32)的降解。

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