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Catabolism of N-acetylneuraminic acid, a fitness function of the food-borne lactic acid bacterium Lactobacillus sakei, involves two newly characterized proteins

机译:N-乙酰神经氨酸的分解代谢是食源性乳酸菌清酒乳杆菌的适应性函数,涉及两种新表征的蛋白质

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摘要

In silico analysis of the genome sequence of the meat-borne lactic acid bacterium (LAB) Lactobacillus sakei 23K has revealed a repertoire of potential functions related to the adaptation of this bacterium to the meat environment. Among these functions, the ability to use N-acetyl-neuraminic acid (NANA) as a carbon source could provide a competitive advantage for growth on meat in which this amino sugar is present. In this work, we proposed to analyze the functionality of a gene cluster encompassing nanTEAR and nanK (nanTEAR-nanK). We established that this cluster encoded a pathway allowing transport and early steps of the catabolism of NANA in this genome. We also demonstrated that this cluster was absent from the genome of other L. sakei strains that were shown to be unable to grow on NANA. Moreover, L. sakei 23K nanA, nanT, nanK, and nanE genes were able to complement Escherichia coli mutants. Construction of different mutants in L. sakei 23K nanR, nanT, and nanK and the double mutant L. sakei 23K (nanA-nanE) made it possible to show that all were impaired for growthon NANA. In addition, two genes located downstream from nanK, lsa1644 and lsa1645, are involved in the catabolism of sialic acid in L. sakei 23K, as a L. sakei 23K lsa1645 mutant was no longer able to grow on NANA. All these results demonstrate that the gene cluster nanTEAR-nanK-lsa1644-lsa1645 is indeed involved in the use of NANA as an energy source by L. sakei.
机译:在对肉源性乳酸菌 (LAB) 清酒乳杆菌 23K 的基因组序列进行计算机分析时,揭示了与该细菌适应肉类环境相关的一系列潜在功能。在这些功能中,使用N-乙酰神经氨酸(NANA)作为碳源的能力可以为存在这种氨基糖的肉类的生长提供竞争优势。在这项工作中,我们提出分析包含nanTEAR和nanK(nanTEAR-nanK)的基因簇的功能。我们确定该簇编码了一条通路,允许该基因组中NANA分解代谢的运输和早期步骤。我们还证明,该簇在其他被证明无法在NANA上生长的L. sakei菌株的基因组中不存在。此外,清酒乳杆菌23K nanA、nanT、nanK和nanE基因能够互补大肠杆菌突变体。在清酒乳杆菌 23K nanR、nanT 和 nanK 中构建不同的突变体以及双突变体清酒乳杆菌 23K (nanA-nanE) 可以证明它们在 NANA 上的生长受损。此外,位于 nanK 下游的两个基因 lsa1644 和 lsa1645 参与了 L. sakei 23K 中唾液酸的分解代谢,因为 L. sakei 23K lsa1645 突变体不再能够在 NANA 上生长。所有这些结果都表明,基因簇nanTEAR-nanK-lsa1644-lsa1645确实参与了清酒乳杆菌利用NANA作为能量来源。

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