Ellington M J K, Richardson D J, Ferguson S J
Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Centre for Metalloprotein Spectroscopy and Biology, School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ, UK.
Microbiology (Reading). 2003 Apr;149(Pt 4):941-948. doi: 10.1099/mic.0.26090-0.
Rhodobacter capsulatus N22DNAR(+) possesses a periplasmic nitrate reductase and is capable of reducing nitrate to nitrite under anaerobic conditions. In the absence of light this ability cannot support chemoheterotrophic growth in batch cultures. This study investigated the effect of nitrate reduction on the growth of R. capsulatus N22DNAR(+) during multiple light-dark cycles of anaerobic photoheterotrophic/dark chemoheterotrophic growth conditions in carbon-limited continuous cultures. The reduction of nitrate did not affect the photoheterotrophic growth yield of R. capsulatus N22DNAR(+). After a transition from photoheterotrophic to dark chemoheterotrophic growth conditions, the reduction of nitrate slowed the initial washout of a R. capsulatus N22DNAR(+) culture. Towards the end of a period of darkness nitrate-reducing cultures maintained higher viable cell counts than non-nitrate-reducing cultures. During light-dark cycling of a mixed culture, the strain able to reduce nitrate (N22DNAR(+)) outcompeted the strain which was unable to reduce nitrate (N22). The evidence indicates that the periplasmic nitrate reductase activity supports slow growth that retards the washout of a culture during anaerobic chemoheterotrophic conditions, and provides a protonmotive force for cell maintenance during the dark period before reillumination. This translates into a selective advantage during repeated light-dark cycles, such that in mixed culture N22DNAR(+) outcompetes N22. Exposure to light-dark cycles will be a common feature for R. capsulatus in its natural habitats, and this study shows that nitrate respiration may provide a selective advantage under such conditions.
荚膜红细菌N22DNAR(+)具有周质硝酸还原酶,能够在厌氧条件下将硝酸盐还原为亚硝酸盐。在无光条件下,这种能力无法支持分批培养中的化学异养生长。本研究调查了在碳限制连续培养的厌氧光异养/黑暗化学异养生长条件的多个明暗循环过程中,硝酸盐还原对荚膜红细菌N22DNAR(+)生长的影响。硝酸盐的还原不影响荚膜红细菌N22DNAR(+)的光异养生长产量。从光异养生长条件转变为黑暗化学异养生长条件后,硝酸盐的还原减缓了荚膜红细菌N22DNAR(+)培养物的初始洗脱。在黑暗期接近尾声时,能够还原硝酸盐的培养物比不能还原硝酸盐的培养物保持更高的活细胞数。在混合培养的明暗循环过程中,能够还原硝酸盐的菌株(N22DNAR(+))比不能还原硝酸盐的菌株(N22)更具竞争力。证据表明,周质硝酸还原酶活性支持缓慢生长,在厌氧化学异养条件下减缓培养物的洗脱,并在重新光照前的黑暗期为细胞维持提供质子动力。这在重复的明暗循环过程中转化为一种选择优势,使得在混合培养中N22DNAR(+)比N22更具竞争力。对于荚膜红细菌来说,暴露于明暗循环将是其自然栖息地中的一个常见特征,本研究表明,在这种条件下硝酸盐呼吸可能提供一种选择优势。