生物化学
裂解酶
亮氨酸
分解代谢
异戊酸盐
生物
辅酶A
突变体
酶
化学
基因
氨基酸
还原酶
发酵
丁酸盐
作者
Mauricio Nahuam Chávez-Avilés,Alma Laura Díaz-Pérez,Homero Reyes de la Cruz,Jesús Campos-Garcı́a
出处
期刊:Fems Microbiology Letters
[Oxford University Press]
日期:2009-05-07
卷期号:296 (1): 117-123
被引量:15
标识
DOI:10.1111/j.1574-6968.2009.01624.x
摘要
The enzymes involved in the catabolism of leucine are encoded by the liu gene cluster in Pseudomonas aeruginosa PAO1. A mutant in the liuE gene (ORF PA2011) of P. aeruginosa was unable to utilize both leucine/isovalerate and acyclic terpenes as the carbon source. The liuE mutant grown in culture medium with citronellol accumulated metabolites of the acyclic terpene pathway, suggesting an involvement of liuE in both leucine/isovalerate and acyclic terpene catabolic pathways. The LiuE protein was expressed as a His-tagged recombinant polypeptide purified by affinity chromatography in Escherichia coli. LiuE showed a mass of 33 kDa under denaturing and 79 kDa under nondenaturing conditions. Protein sequence alignment and fingerprint sequencing suggested that liuE encodes 3-hydroxy-3-methylglutaryl-coenzyme A lyase (HMG-CoA lyase), which catalyzes the cleavage of HMG-CoA to acetyl-CoA and acetoacetate. LiuE showed HMG-CoA lyase optimal activity at a pH of 7.0 and 37 degrees C, an apparent K(m) of 100 microM for HMG-CoA and a V(max) of 21 micromol min(-1) mg(-1). These results demonstrate that the liuE gene of P. aeruginosa encodes for the HMG-CoA lyase, an essential enzyme for growth in both leucine and acyclic terpenes.
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