Institute for Microbiology, Technische Universität Braunschweig, Braunschweig, Germany.
J Bacteriol. 2013 Oct;195(20):4769-77. doi: 10.1128/JB.00860-13. Epub 2013 Aug 23.
Anaerobic growth and survival are integral parts of the life cycle of many marine bacteria. To identify genes essential for the anoxic life of Dinoroseobacter shibae, a transposon library was screened for strains impaired in anaerobic denitrifying growth. Transposon insertions in 35 chromosomal and 18 plasmid genes were detected. The essential contribution of plasmid genes to anaerobic growth was confirmed with plasmid-cured D. shibae strains. A combined transcriptome and proteome approach identified oxygen tension-regulated genes. Transposon insertion sites of a total of 1,527 mutants without an anaerobic growth phenotype were determined to identify anaerobically induced but not essential genes. A surprisingly small overlap of only three genes (napA, phaA, and the Na(+)/Pi antiporter gene Dshi_0543) between anaerobically essential and induced genes was found. Interestingly, transposon mutations in genes involved in dissimilatory and assimilatory nitrate reduction (napA, nasA) and corresponding cofactor biosynthesis (genomic moaB, moeB, and dsbC and plasmid-carried dsbD and ccmH) were found to cause anaerobic growth defects. In contrast, mutation of anaerobically induced genes encoding proteins required for the later denitrification steps (nirS, nirJ, nosD), dimethyl sulfoxide reduction (dmsA1), and fermentation (pdhB1, arcA, aceE, pta, acs) did not result in decreased anaerobic growth under the conditions tested. Additional essential components (ferredoxin, cccA) of the anaerobic electron transfer chain and central metabolism (pdhB) were identified. Another surprise was the importance of sodium gradient-dependent membrane processes and genomic rearrangements via viruses, transposons, and insertion sequence elements for anaerobic growth. These processes and the observed contributions of cell envelope restructuring (lysM, mipA, fadK), C4-dicarboxylate transport (dctM1, dctM3), and protease functions to anaerobic growth require further investigation to unravel the novel underlying adaptation strategies.
厌氧生长和存活是许多海洋细菌生命周期的重要组成部分。为了鉴定对狄氏弧菌(Dinoroseobacter shibae)乏氧反硝化生长至关重要的基因,我们筛选了转座子文库,以鉴定在厌氧反硝化生长中受到损伤的菌株。在 35 个染色体基因和 18 个质粒基因中检测到转座子插入。用质粒消除的狄氏弧菌菌株证实了质粒基因对厌氧生长的重要贡献。联合转录组和蛋白质组学方法鉴定了氧张力调节基因。总共确定了 1527 个没有厌氧生长表型的突变体的转座子插入位点,以鉴定厌氧诱导但不是必需的基因。在必需基因和诱导基因之间仅发现三个基因(napA、phaA 和 Na(+)/Pi 反向转运蛋白基因 Dshi_0543)的重叠非常小。有趣的是,参与异化和同化硝酸盐还原(napA、nasA)和相应辅助因子生物合成(基因组 moaB、moeB 和 dsbC 以及质粒携带的 dsbD 和 ccmH)的基因中的转座子突变被发现导致厌氧生长缺陷。相比之下,突变厌氧诱导基因编码用于随后的反硝化步骤(nirS、nirJ、nosD)、二甲基亚砜还原(dmsA1)和发酵(pdhB1、arcA、aceE、pta、acs)所需的蛋白质不会导致在测试条件下厌氧生长减少。还鉴定了厌氧电子传递链和中心代谢(pdhB)的其他必需成分(铁氧还蛋白、cccA)。另一个惊喜是,钠离子梯度依赖的膜过程和通过病毒、转座子和插入序列元件的基因组重排对厌氧生长的重要性。这些过程以及观察到的细胞包膜重构(lysM、mipA、fadK)、C4-二羧酸转运(dctM1、dctM3)和蛋白酶功能对厌氧生长的贡献需要进一步研究,以揭示新的潜在适应策略。