瘤胃木兰氏菌产生丙酸盐与钴胺素依赖性相关的转录组和蛋白质组变化

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-10-29 DOI:10.1128/msystems.00864-24
Sam C Mahoney-Kurpe, Nikola Palevich, Dragana Gagic, Patrick J Biggs, Peter M Reid, Ianina Altshuler, Phillip B Pope, Graeme T Attwood, Christina D Moon
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引用次数: 0

摘要

反刍木兰氏菌是一种丰富的瘤胃细菌,它以依赖钴胺(维生素 B12)的方式通过琥珀酸途径产生丙酸盐。然而,这种情况在瘤胃木兰氏菌和密切相关的细菌中发生的程度,以及补充钴胺素对丙酸盐途径基因和酶表达的影响还有待研究。为了评估这一点,我们筛选了 14 个菌株,发现几乎所有菌株在补充钴胺素时都会产生丙酸盐。我们选择了 X. ruminicola KHP1 进行进一步研究,包括对其进行全基因组测序,以及对添加和不添加钴胺素的 KHP1 培养物进行转录组学和蛋白质组学比较。在完整的 KHP1 基因组中搜索了与钴胺素结合的核糖开关,预测出了四个,但没有一个与任何琥珀酸通路基因密切相关,这些基因分散在许多基因组位点上。补充钴胺素导致 17.5% 的基因差异表达,包括编码依赖钴胺素的甲基丙二酰-CoA 突变酶和一些甲基丙二酰-CoA 脱羧酶亚基的基因,但大多数丙酸酯生物合成途径基因没有差异表达。补充钴胺素对 KHP1 蛋白体组的影响要小得多,唯一表达量不同的丙酸酯途径酶是甲基丙二酰-CoA 突变酶,在补充钴胺素时,该酶的表达量更高。我们的研究结果表明,补充钴胺素不会诱导整个丙酸酯生物合成途径,但会持续增加甲基丙二酰-CoA 突变酶在转录组和蛋白质组水平的表达。与预测的钴胺素核糖开关附近的基因相比,观察到的丙酸盐途径基因差异表达的幅度较小:在反刍动物中,瘤胃微生物群落通过发酵饲料为宿主动物提供重要的能量基质,在营养方面发挥着至关重要的作用。丙酸盐是瘤胃发酵的主要终产物,鉴于其在宿主葡萄糖生产中的重要性以及对温室气体生产的影响,提高丙酸盐的产量是可取的。维生素 B12(钴胺素)能诱导重要的瘤胃细菌 Xylanibacter ruminicola 产生丙酸盐,但钴胺素如何调节丙酸盐途径的活性还不完全清楚。与预期相反,我们发现在转录组和蛋白质组水平上,补充钴胺素对丙酸盐途径的表达几乎没有影响,只是该途径中钴胺素依赖酶的编码基因略有上调。这些发现为丙酸盐生产的调控因素提供了新的见解,并表明反刍动物X.依赖钴胺素的丙酸盐生产是由翻译后控制的。
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Transcriptomic and proteomic changes associated with cobalamin-dependent propionate production by the rumen bacterium Xylanibacter ruminicola.

Xylanibacter ruminicola is an abundant rumen bacterium that produces propionate in a cobalamin (vitamin B12)-dependent manner via the succinate pathway. However, the extent to which this occurs across ruminal Xylanibacter and closely related bacteria, and the effect of cobalamin supplementation on the expression of propionate pathway genes and enzymes has yet to be investigated. To assess this, we screened 14 strains and found that almost all strains produced propionate when supplemented with cobalamin. X. ruminicola KHP1 was selected for further study, including complete genome sequencing, and comparative transcriptomics and proteomics of KHP1 cultures grown with and without supplemented cobalamin. The complete KHP1 genome was searched for cobalamin-binding riboswitches and four were predicted, though none were closely located to any of the succinate pathway genes, which were dispersed at numerous genomic loci. Cobalamin supplementation led to the differential expression of 17.5% of genes, including genes encoding the cobalamin-dependent methylmalonyl-CoA mutase and some methylmalonyl-CoA decarboxylase subunits, but most propionate biosynthesis pathway genes were not differentially expressed. The effect of cobalamin supplementation on the KHP1 proteome was much less pronounced, with the only differentially abundant propionate pathway enzyme being methylmalonyl-CoA mutase, which had greater abundance when supplemented with cobalamin. Our results demonstrate that cobalamin supplementation does not result in induction of the entire propionate biosynthesis pathway, but consistently increased expression of methylmalonyl-CoA mutase at transcriptome and proteome levels. The magnitude of the differential expression of propionate pathway genes observed was minor compared to that of genes proximate to predicted cobalamin riboswitches.

Importance: In ruminants, the rumen microbial community plays a critical role in nutrition through the fermentation of feed to provide vital energy substrates for the host animal. Propionate is a major rumen fermentation end-product and increasing its production is desirable given its importance in host glucose production and impact on greenhouse gas production. Vitamin B12 (cobalamin) can induce propionate production in the prominent rumen bacterium Xylanibacter ruminicola, but it is not fully understood how cobalamin regulates propionate pathway activity. Contrary to expectation, we found that cobalamin supplementation had little effect on propionate pathway expression at transcriptome and proteome levels, with minor upregulation of genes encoding the cobalamin-dependent enzyme of the pathway. These findings provide new insights into factors that regulate propionate production and suggest that cobalamin-dependent propionate production by X. ruminicola is controlled post-translationally.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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