Baumann B, Snozzi M, Zehnder A J, Van Der Meer J R
Swiss Federal Institute of Environmental Science and Technology, Dubendorf, Switzerland.
J Bacteriol. 1996 Aug;178(15):4367-74. doi: 10.1128/jb.178.15.4367-4374.1996.
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.
在反硝化副球菌的连续培养中,研究了从好氧生长条件转变为厌氧生长条件以及反之转变过程中反硝化活性的诱导和抑制情况。通过测量反硝化产物(亚硝酸盐、一氧化氮、一氧化二氮和氮气)的形成、硝酸盐、亚硝酸盐和一氧化二氮还原酶的个体mRNA水平以及用针对cd1型亚硝酸盐还原酶的多克隆抗体检测亚硝酸盐还原酶的浓度,来监测细胞的反硝化活性。从好氧呼吸转变为厌氧呼吸时,培养物进入一个不稳定的过渡阶段,在此期间反硝化途径被诱导。这个阶段的开始表现为各个反硝化酶的mRNA水平增加15至45倍。所有mRNA在短时间内积累,之后它们的总体浓度下降,达到一个略高于好氧稳态条件下观察到的值的稳定值。有趣的是,最早形成的mRNA是硝酸盐和一氧化二氮还原酶的mRNA。亚硝酸盐还原酶mRNA出现得明显更晚,这表明这三个基因的调控模式不同。与mRNA水平不同,亚硝酸盐还原酶蛋白的水平在厌氧期间缓慢增加,在转换后约30小时达到稳定值。所有反硝化中间产物都可以短暂观察到,但当达到新的厌氧稳态时,氮气是主要产物。当厌氧培养物转回好氧呼吸时,细胞的反硝化立即停止,尽管仍然存在足够的亚硝酸盐还原酶。我们可以观察到各个反硝化酶的mRNA水平略有下降,回到其好氧、未诱导的水平。在好氧期间,亚硝酸盐还原酶蛋白没有被积极降解。