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MrpA 在依赖乙酸盐的 Methanosarcina acetivorans 生长过程中的能量转换中发挥作用。

MrpA functions in energy conversion during acetate-dependent growth of Methanosarcina acetivorans.

机构信息

Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania, USA.

出版信息

J Bacteriol. 2013 Sep;195(17):3987-94. doi: 10.1128/JB.00581-13. Epub 2013 Jul 8.

Abstract

The role of the multisubunit sodium/proton antiporter (Mrp) of Methanosarcina acetivorans was investigated with a mutant deleted for the gene encoding the MrpA subunit. Antiporter activity was 5-fold greater in acetate-grown versus methanol-grown wild-type cells, consistent with the previously published relative levels of mrp transcript. The rate, final optical density, and dry weight/methane ratio decreased for the mutant versus wild type when cultured with a growth-limiting concentration of acetate. All growth parameters of the mutant or wild type were identical when grown with methanol in medium containing a growth-limiting Na(+) concentration of 1.04 M. The lag phase, growth rate, and final optical density for growth of the mutant were suboptimal compared to the wild type when cultured with acetate in medium containing either 0.54 or 1.04 M Na(+). The addition of 25 mM NaCl to resting cell suspensions stimulated ATP synthesis driven by a potassium diffusion potential. ATP synthesis was greater in wild-type than mutant cells grown with acetate, a trend that held for methanol-grown cells, albeit less pronounced. Both sodium and proton ionophores reduced ATP synthesis in the wild type grown with either substrate. The results indicated that the Mrp complex is essential for efficient ATP synthesis and optimal growth at the low concentrations of acetate encountered in the environment.

摘要

甲烷八叠球菌多亚基钠离子/质子反向转运体(Mrp)的作用,通过一个缺失编码 MrpA 亚基基因的突变体进行了研究。与甲醇生长的野生型细胞相比,乙酸盐生长的反向转运体活性高 5 倍,这与先前发表的 mrp 转录本的相对水平一致。当用生长受限浓度的乙酸盐培养时,与野生型相比,突变体的速率、最终光密度和干重/甲烷比降低。当用甲醇在含有生长受限的 1.04 M Na+浓度的培养基中培养时,突变体或野生型的所有生长参数均相同。与野生型相比,当用含有 0.54 或 1.04 M Na+的培养基中用乙酸盐培养时,突变体的迟滞期、生长速率和最终光密度均不理想。向静止细胞悬浮液中添加 25 mM NaCl 可刺激由钾扩散势驱动的 ATP 合成。与生长在乙酸盐中的突变体相比,在生长在乙酸盐中的野生型细胞中 ATP 合成更多,尽管趋势不太明显。在生长有两种底物的野生型细胞中,钠离子和质子载体都降低了 ATP 的合成。结果表明,Mrp 复合物对于在环境中遇到的低浓度乙酸盐的有效 ATP 合成和最佳生长是必不可少的。

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