Marietou Angeliki, Røy Hans, Jørgensen Bo B, Kjeldsen Kasper U
Center for Geomicrobiology, Department of Bioscience, Aarhus University, Aarhus, Denmark.
Front Microbiol. 2018 Mar 2;9:309. doi: 10.3389/fmicb.2018.00309. eCollection 2018.
The first step in the sulfate reduction pathway is the transport of sulfate across the cell membrane. This uptake has a major effect on sulfate reduction rates. Much of the information available on sulfate transport was obtained by studies on assimilatory sulfate reduction, where sulfate transporters were identified among several types of protein families. Despite our growing knowledge on the physiology of dissimilatory sulfate-reducing microorganisms (SRM) there are no studies identifying the proteins involved in sulfate uptake in members of this ecologically important group of anaerobes. We surveyed the complete genomes of 44 sulfate-reducing bacteria and archaea across six phyla and identified putative sulfate transporter encoding genes from four out of the five surveyed protein families based on homology. We did not find evidence that ABC-type transporters (SulT) are involved in the uptake of sulfate in SRM. We speculate that members of the CysP sulfate transporters could play a key role in the uptake of sulfate in thermophilic SRM. Putative CysZ-type sulfate transporters were present in all genomes examined suggesting that this overlooked group of sulfate transporters might play a role in sulfate transport in dissimilatory sulfate reducers alongside SulP. Our analysis highlights several targets for further molecular studies in order to understand this key step in the metabolism of SRMs.
硫酸盐还原途径的第一步是硫酸盐跨细胞膜的转运。这种摄取对硫酸盐还原速率有重大影响。关于硫酸盐转运的许多现有信息是通过对同化性硫酸盐还原的研究获得的,在这些研究中,在几种蛋白质家族类型中鉴定出了硫酸盐转运蛋白。尽管我们对异化性硫酸盐还原微生物(SRM)的生理学了解越来越多,但尚无研究鉴定出参与这一具有重要生态意义的厌氧菌群中硫酸盐摄取的蛋白质。我们调查了六个门中44种硫酸盐还原细菌和古菌的完整基因组,并基于同源性从五个被调查的蛋白质家族中的四个中鉴定出了假定的硫酸盐转运蛋白编码基因。我们没有发现证据表明ABC型转运蛋白(SulT)参与SRM中硫酸盐的摄取。我们推测,CysP硫酸盐转运蛋白成员可能在嗜热SRM的硫酸盐摄取中起关键作用。在所有检测的基因组中都存在假定的CysZ型硫酸盐转运蛋白,这表明这一被忽视的硫酸盐转运蛋白组可能在异化性硫酸盐还原菌的硫酸盐转运中与SulP一起发挥作用。我们的分析突出了几个进一步进行分子研究的靶点,以便了解SRM代谢中的这一关键步骤。