Chae Jong-Chan, Song Bongkeun, Zylstra Gerben J
Biotechnology Center for Agriculture and the Environment, School of Environmental and Biological Sciences, Rutgers University, New Brunswick, NJ 08901-8520, USA.
FEMS Microbiol Lett. 2008 Apr;281(2):203-9. doi: 10.1111/j.1574-6968.2008.01106.x. Epub 2008 Mar 18.
A metagenomic approach was taken to investigate the genetic basis for the ability of an anaerobic consortium to grow on either 4-chlorobenzoate or 4-bromobenzoate under denitrifying conditions. Degenerate PCR primers were designed for the family of 4-chlorobenzoyl-CoA dehalogenase genes. The primers were utilized to screen a metagenome library and two overlapping clones were identified which yield a PCR product. The complete sequence of one metagenome clone was determined and genes encoding 4-chlorobenzoyl-CoA ligase (FcbA) and 4-chlorobenzoyl-CoA dehalogenase (FcbB) were identified. Analysis of the ORFs present in the nucleotide sequence suggests that the metagenome clone originated from an uncultured denitrifying microorganism belonging to the Betaproteobacteria. Interestingly, unlike similar gene clusters reported in aerobes, a gene encoding 4-hydroxybenzoyl-CoA thioesterase was not present in the gene cluster. This suggests that 4-hydroxybenzoyl-CoA is further degraded via the anaerobic reduction pathway in the corresponding microorganism instead of through thioester hydrolysis to yield 4-hydroxybenzoate.
采用宏基因组学方法研究了一个厌氧菌群在反硝化条件下以4-氯苯甲酸或4-溴苯甲酸为底物生长的遗传基础。针对4-氯苯甲酰辅酶A脱卤酶基因家族设计了简并PCR引物。利用这些引物筛选宏基因组文库,鉴定出两个重叠克隆,它们产生了PCR产物。测定了一个宏基因组克隆的完整序列,并鉴定出编码4-氯苯甲酰辅酶A连接酶(FcbA)和4-氯苯甲酰辅酶A脱卤酶(FcbB)的基因。对核苷酸序列中存在的开放阅读框的分析表明,该宏基因组克隆来源于一种未培养的属于β-变形菌纲的反硝化微生物。有趣的是,与需氧菌中报道的类似基因簇不同,该基因簇中不存在编码4-羟基苯甲酰辅酶A硫酯酶的基因。这表明在相应的微生物中,4-羟基苯甲酰辅酶A是通过厌氧还原途径进一步降解的,而不是通过硫酯水解产生4-羟基苯甲酸。