Propionate metabolism in Desulfurella acetivorans.

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2025-02-12 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1545849
Eugenio Pettinato, Thomas M Steiner, Eric A Cassens, Thomas Geisberger, Christian Seitz, Simone König, Wolfgang Eisenreich, Ivan A Berg
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Abstract

Desulfurella acetivorans is a strictly anaerobic sulfur-reducing deltaproteobacterium that can grow heterotrophically by oxidation of acetate or autotrophically with molecular hydrogen. Here we show that D. acetivorans possesses a putative operon encoding enzymes of the methylcitrate cycle of propionate oxidation and demonstrate that this bacterium is capable of propionate growth. However, activities of the methylcitrate cycle enzymes could not be detected in extracts of propionate-grown cells, and experiments with [U-13C3]propionate and comparative proteomic analysis of acetate- and propionate-grown cells suggested that the methylcitrate cycle is not active during propionate growth. Instead, propionyl-CoA assimilation proceeds via its carboxylation to methylmalonyl-CoA, which is further converted to succinyl-CoA. The latter is directed to the tricarboxylic acid (TCA) cycle, where it is converted to oxaloacetate and condenses with acetyl-CoA (produced by decarboxylation of another oxaloacetate molecule) to form citrate, which is oxidized in the TCA cycle. These results highlight the uncertainty of genomic predictions in the analysis of microbial metabolic pathways and the need for their experimental confirmation.

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活性脱硫草丙酸代谢。
Desulfurella acetivorans是一种严格厌氧的硫还原三角洲变形菌,可以通过醋酸氧化异养生长或与分子氢自养生长。在这里,我们证明了D. acetivorans具有一个假定的操纵子编码丙酸氧化甲基柠檬酸循环的酶,并证明了这种细菌能够丙酸生长。然而,在丙酸盐培养的细胞提取物中没有检测到甲基柠檬酸循环酶的活性,用[U-13C3]丙酸盐进行的实验以及乙酸和丙酸盐培养的细胞的比较蛋白质组学分析表明,甲基柠檬酸循环在丙酸盐生长过程中没有活性。相反,丙酰辅酶a的同化过程通过羧基化转化为甲基丙二酰辅酶a,甲基丙二酰辅酶a进一步转化为琥珀酰辅酶a。后者被引导到三羧酸(TCA)循环,在那里它被转化为草酰乙酸,并与乙酰辅酶a(由另一种草酰乙酸分子脱羧产生)缩合形成柠檬酸盐,柠檬酸盐在TCA循环中被氧化。这些结果突出了微生物代谢途径分析中基因组预测的不确定性以及对其实验证实的必要性。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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