首页> 美国卫生研究院文献>Journal of Bacteriology >Reduction of the amount of periplasmic hydrogenase in Desulfovibrio vulgaris (Hildenborough) with antisense RNA: direct evidence for an important role of this hydrogenase in lactate metabolism.
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Reduction of the amount of periplasmic hydrogenase in Desulfovibrio vulgaris (Hildenborough) with antisense RNA: direct evidence for an important role of this hydrogenase in lactate metabolism.

机译:用反义RNA减少寻常脱硫弧菌(希尔登伯勒)中周质氢化酶的量:直接证明这种氢化酶在乳酸代谢中的重要作用。

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摘要

To establish the function of the periplasmic Fe-only hydrogenase in the anaerobic sulfate reducer Desulfovibrio vulgaris (Hildenborough), derivatives with a reduced content of this enzyme were constructed by introduction of a plasmid that directs the synthesis of antisense RNA complementary to hydrogenase mRNA. It was demonstrated that the antisense RNA technique allowed specific suppression of the synthesis of this hydrogenase in D. vulgaris by decreasing the amount of hydrogenase mRNA but did not result in the complete elimination of the enzyme, as is usual with most conventional mutagenesis techniques. The hydrogenase content in these antisense RNA-producing D. vulgaris clones was two- to threefold lower than in the parental strain when the strains were grown in batch cultures with lactate as a substrate and sulfate as a terminal electron acceptor. Under these conditions, several differences in growth parameters were measured between the hydrogenase-suppressed clones and wild-type D. vulgaris: growth rates of the clones decreased two- to threefold, and at excess lactate, growth yields were reduced by 20%. Furthermore, the amount of hydrogen measured in the culture headspaces was reduced three- to fivefold for the clones. These observations indicate that this hydrogenase has an important function during growth on lactate and is involved in hydrogen production from protons and electrons originating from at least one of the two oxidation reactions in the conversion of lactate to acetate. The implications for the energy metabolism of D. vulgaris are discussed.
机译:为了确定厌氧硫酸盐还原剂Desulfovibrio vulgaris(Hildenborough)中仅含铁质质的加氢酶的功能,通过引入质粒来构建该酶含量降低的衍生物,该质粒指导合成与加氢酶mRNA互补的反义RNA。事实证明,反义RNA技术可通过减少氢化酶mRNA的量来特异性抑制寻常小球藻中该氢化酶的合成,但并不能像大多数常规诱变技术一样完全消除该酶。当这些菌株在以乳酸为底物,硫酸盐为末端电子受体的分批培养中生长时,这些反义的产生RNA的寻常双歧杆菌克隆中的氢化酶含量比亲本菌株低2-3倍。在这些条件下,测量了氢化酶抑制的克隆和野生型D. D.寻常的生长参数的几个差异:克隆的生长速度降低了2到3倍,而乳酸过量时,生长产量降低了20%。此外,对于克隆,在培养顶空中测得的氢气量减少了三到五倍。这些观察结果表明,该加氢酶在乳酸上的生长过程中具有重要的功能,并且参与了从乳酸到乙酸的转化中两个氧化反应中至少一个的质子和电子产生的氢。讨论了对普通小球藻能量代谢的影响。

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