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与瘤胃细菌依赖钴胺素的丙酸生产相关的转录组学和蛋白质组学变化。

Transcriptomic and proteomic changes associated with cobalamin-dependent propionate production by the rumen bacterium .

机构信息

AgResearch Ltd, Grasslands Research Centre, Palmerston North, New Zealand.

School of Food Technology and Natural Sciences, Massey University, Palmerston North, New Zealand.

出版信息

mSystems. 2024 Nov 19;9(11):e0086424. doi: 10.1128/msystems.00864-24. Epub 2024 Oct 29.

Abstract

UNLABELLED

is an abundant rumen bacterium that produces propionate in a cobalamin (vitamin B)-dependent manner via the succinate pathway. However, the extent to which this occurs across ruminal 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. 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 B (cobalamin) can induce propionate production in the prominent rumen bacterium , 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 is controlled post-translationally.

摘要

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是一种丰富的瘤胃细菌,通过琥珀酸途径以钴胺素(维生素 B)依赖性方式产生丙酸盐。然而,这种情况在瘤胃和密切相关的细菌中发生的程度,以及钴胺素补充对丙酸盐途径基因和酶表达的影响尚未得到研究。为了评估这一点,我们筛选了 14 株菌株,发现几乎所有菌株在补充钴胺素时都会产生丙酸盐。选择 KHP1 进行进一步研究,包括完整基因组测序,以及在有和没有补充钴胺素的情况下培养 KHP1 培养物的比较转录组学和蛋白质组学。搜索完整的 KHP1 基因组以寻找钴胺素结合的核糖开关,预测到了四个,但没有一个与琥珀酸途径基因紧密相关,这些基因分散在许多基因组位点上。钴胺素补充导致 17.5%的基因表达差异,包括编码钴胺素依赖性甲基丙二酰辅酶 A 变位酶和一些甲基丙二酰辅酶 A 脱羧酶亚基的基因,但大多数丙酸盐生物合成途径基因没有差异表达。钴胺素补充对 KHP1 蛋白质组的影响要小得多,唯一差异丰富的丙酸盐途径酶是甲基丙二酰辅酶 A 变位酶,当补充钴胺素时其丰度更高。我们的结果表明,钴胺素补充不会导致整个丙酸盐生物合成途径的诱导,但始终会增加甲基丙二酰辅酶 A 变位酶在转录组和蛋白质组水平上的表达。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。

重要性

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底物,在营养方面发挥着关键作用。丙酸盐是主要的瘤胃发酵终产物,增加其产量是可取的,因为它对宿主葡萄糖产生和对温室气体产生的影响很重要。维生素 B(钴胺素)可以诱导主要的瘤胃细菌 产生丙酸盐,但尚不完全清楚钴胺素如何调节丙酸盐途径的活性。与预期相反,我们发现,在转录组和蛋白质组水平上,钴胺素补充对丙酸盐途径的表达几乎没有影响,该途径的依赖钴胺素的酶的基因表达略有上调。这些发现为调节丙酸盐产生的因素提供了新的见解,并表明 依赖钴胺素的丙酸盐产生受翻译后调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212e/11575231/48939c87b685/msystems.00864-24.f001.jpg

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