Le Guen L, Santos R, Camadro J M
Département de Microbiologie, Institut Jacques-Monod, UMR 7592-CNRS-Universités Paris, France.
FEMS Microbiol Lett. 1999 Apr 1;173(1):175-82. doi: 10.1111/j.1574-6968.1999.tb13499.x.
The Escherichia coli hemK gene has been described as being involved in protoporphyrinogen oxidase activity; however, there is no biochemical evidence for this. In the context of characterizing the mechanisms of protoporphyrinogen oxidation in the yeast Saccharomyces cerevisiae, we investigated the yeast homolog of HemK, which is encoded by the ORF YNL063w, to find out whether it has any protoporphyrinogen oxidase activity and/or whether it modulates protoporphyrinogen oxidase activity. Phenotype analysis and enzyme activity measurements indicated that the yeast HemK homolog is not involved in protoporphyrinogen oxidase activity. Complementation assays in which the yeast HemK homolog is overproduced do not restore wild-type phenotypes in a yeast strain with deficient protoporphyrinogen oxidase activity. Protein sequence analysis of HemK-related proteins revealed consensus motif for S-adenosyl-methionine-dependent methyltransferase.
大肠杆菌hemK基因被认为与原卟啉原氧化酶活性有关;然而,目前尚无相关生化证据。在对酿酒酵母中原卟啉原氧化机制进行表征的背景下,我们研究了由开放阅读框YNL063w编码的HemK酵母同源物,以确定它是否具有原卟啉原氧化酶活性和/或是否调节原卟啉原氧化酶活性。表型分析和酶活性测量表明,酵母HemK同源物不参与原卟啉原氧化酶活性。在原卟啉原氧化酶活性缺陷的酵母菌株中,过量表达酵母HemK同源物的互补试验不能恢复野生型表型。对HemK相关蛋白的蛋白质序列分析揭示了S-腺苷甲硫氨酸依赖性甲基转移酶的共有基序。