首页> 美国卫生研究院文献>Journal of Bacteriology >Dynamics of denitrification activity of Paracoccus denitrificans in continuous culture during aerobic-anaerobic changes.
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Dynamics of denitrification activity of Paracoccus denitrificans in continuous culture during aerobic-anaerobic changes.

机译:有氧-无氧变化期间连续培养过程中反硝化副球菌反硝化活性的动力学。

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摘要

Induction and repression of denitrification activity were studied in a continuous culture of Paracoccus denitrificans during changes from aerobic to anaerobic growth conditions and vice versa. The denitrification activity of the cells was monitored by measuring the formation of denitrification products (nitrite, nitric oxide, nitrous oxide, and dinitrogen), individual mRNA levels for the nitrate, nitrite, and nitrous oxide reductases, and the concentration of the nitrite reductase enzyme with polyclonal antibodies against the cd1-type nitrite reductase. On a change from aerobic to anaerobic respiration, the culture entered an unstable transition phase during which the denitrification pathway became induced. The onset of this phase was formed by a 15- to 45-fold increase of the mRNA levels for the individual denitrification enzymes. All mRNAs accumulated during a short period, after which their overall concentration declined to reach a stable value slightly higher than that observed under aerobic steady-state conditions. Interestingly, the first mRNAs to be formed were those for nitrate and nitrous oxide reductase. The nitrite reductase mRNA appeared significantly later, suggesting different modes of regulation for the three genes. Unlike the mRNA levels, the level of the nitrite reductase protein increased slowly during the anaerobic period, reaching a stable value about 30 h after the switch. All denitrification intermediates could be observed transiently, but when the new anaerobic steady state was reached, dinitrogen was the main product. When the anaerobic cultures were switched back to aerobic respiration, denitrification of the cells stopped at once, although sufficient nitrite reductase was still present. We could observe that the mRNA levels for the individual denitrification enzymes decreased slightly to their aerobic, uninduced levels. The nitrite reductase protein was not actively degraded during the aerobic period.
机译:在有氧至无氧生长条件下(反之亦然)的过程中,在反硝化副球菌连续培养中研究了反硝化活性的诱导和抑制。通过测量反硝化产物(亚硝酸盐,一氧化氮,一氧化二氮和二氧化氮)的形成,硝酸盐,亚硝酸盐和一氧化二氮还原酶的个别mRNA水平以及亚硝酸盐还原酶的浓度,来监测细胞的反硝化活性。带有针对cd1型亚硝酸还原酶的多克隆抗体。在从有氧呼吸到无氧呼吸的变化中,培养物进入不稳定的过渡阶段,在此期间反硝化途径被诱导。该阶段的开始是通过单个反硝化酶的mRNA水平增加15到45倍而形成的。所有mRNA均在短时间内积累,此后它们的总浓度下降至稳定值,该值略高于有氧稳态条件下观察到的值。有趣的是,首先形成的mRNA是硝酸盐和一氧化二氮还原酶的mRNA。亚硝酸还原酶mRNA的出现时间较晚,这表明这三个基因的调控方式不同。与mRNA水平不同,亚硝酸还原酶蛋白的水平在厌氧期间缓慢增加,在切换后约30小时达到稳定值。可以短暂观察到所有反硝化中间体,但是当达到新的厌氧稳态时,主要成分为二氮。当厌氧培养物切换回有氧呼吸时,尽管仍然存在足够的亚硝酸还原酶,但细胞的反硝化立即停止。我们可以观察到,各个反硝化酶的mRNA水平略微降低至有氧,未诱导水平。在有氧期间,亚硝酸还原酶蛋白没有被主动降解。

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