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插入突变在氢化酶 vhc 和 frc 操纵子编码的甲烷球菌中硒自由氢化酶。

Insertional Mutations in the Hydrogenase vhc and frc Operons Encoding Selenium-Free Hydrogenases in Methanococcus voltae.

出版信息

Appl Environ Microbiol. 1995 May;61(5):1770-5. doi: 10.1128/aem.61.5.1770-1775.1995.

Abstract

Methanococcus voltae, which contains four different gene groups that encode [NiFe]-hydrogenases, was transformed with integration vectors to achieve polar inactivation of two of the four hydrogenase operons that encode the selenium-free enzymes Vhc and Frc. Transformants which were selected by their acquired puromycin resistance showed site-specific insertions in either the vhc or frc operon by single crossover events. Southern hybridization revealed tandem integrations of whole vectors in the vhc operon, whereas only one vector copy was found in the frc operon. Northern (RNA) hybridizations showed a pac transcript of defined size, indicating strong termination in front of the hydrogenase genes downstream. In spite of the apparent abolition of expression of selenium-free hydrogenases through these polar insertions, they were not lethal to cells upon growth in selenium-deprived minimal medium, which we had previously shown to strongly induce transcription of the respective operons in M. voltae. Instead, like wild-type control cultures, transformants responded to selenium deprivation only with a reduction in growth rate. We conclude that loss of the potential to express a selenium-free hydrogenase can nevertheless be balanced by very small amounts of selenium hydrogenases under laboratory conditions in which the hydrogen supply is not likely to be a limiting growth factor.

摘要

产甲烷球菌(Methanococcus voltae)包含四个不同的基因群,这些基因群编码[NiFe]-氢化酶,该细菌通过整合载体进行转化,以实现对编码不含硒酶 Vhc 和 Frc 的四个氢化酶操纵子中的两个的极性失活。通过获得的嘌呤霉素抗性选择的转化体通过单交叉事件显示出在 vhc 或 frc 操纵子中发生了特异性插入。Southern 杂交显示 vhc 操纵子中整个载体的串联整合,而在 frc 操纵子中仅发现一个载体副本。Northern(RNA)杂交显示出具有明确定义大小的 pac 转录物,表明在下游氢化酶基因前有强烈的终止。尽管通过这些极性插入明显消除了不含硒氢化酶的表达,但在我们之前曾表明在缺硒最小培养基中强烈诱导相应操纵子转录的情况下,它们对细胞并没有致死性。相反,与野生型对照培养物一样,转化体仅在生长速率降低时才对硒缺乏作出反应。我们得出结论,在实验室条件下,尽管潜在的表达不含硒氢化酶的能力丧失,但在氢气供应不太可能成为限制生长因素的情况下,仍可以通过非常少量的硒氢化酶来平衡。

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