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通过 NMR 光谱学对包括“Big Six”在内的 8 株大肠杆菌菌株的代谢特征进行分析,并对选定菌株的酸性反应进行研究。

Metabolic characterisation of eight Escherichia coli strains including "Big Six" and acidic responses of selected strains revealed by NMR spectroscopy.

机构信息

Department of Food Science and Technology, National University of Singapore, Singapore, 117542, Singapore; National University of Singapore (Suzhou) Research Institute, 377 Lin Quan Street, Suzhou Industrial Park, Suzhou, Jiangsu, 215123, PR China.

Setsco Services Pte., Ltd., Singapore, 608925, Singapore.

出版信息

Food Microbiol. 2020 Jun;88:103399. doi: 10.1016/j.fm.2019.103399. Epub 2019 Dec 11.

Abstract

The metabolic diversity of Escherichia coli strains (non-pathogenic E. coli ATCC 25922, and pathogenic E. coli O157:H7, O26:H11, O45:H2, O103:H11, O111, O121:H19, and O145) was tested using nuclear magnetic resonance. Based on two representative two-dimensional H-C spectra, 38 metabolites were identified in E. coli intracellular samples. Principal component analysis indicated that metabolites including lysine, arginine, α-ketoglutaric acid, adenosine, and fumaric acid were responsible for the separation of E. coli ATCC 25922. Relatively large metabolic differences between ATCC 25922 and the pathogenic strains were recoded. The most varied pairwise group (ATCC 25922 vs. O26:H11) was further analysed. The screened metabolites and enrichment pathway tests revealed different amino acid metabolism and higher requirement for energy production in the pathogenic strains. The acidic responses of the selected strains were further tested. The in vitro and in vivo inactivation kinetics, morphological changes, and protein leakage showed higher acid tolerance of E. coli O26:H11. Metabolic analysis of the two strains under acidic stress revealed alternative metabolites and pathways in the two groups. Pathogenic O26:H11 was characterised by higher energy production and amino acid metabolism (lysine and glutamic acid). Real-time PCR tests confirmed that glutamic acid dependent decarboxylase/antiporter system was the major acid resistance mechanism.

摘要

使用核磁共振技术测试了大肠杆菌菌株(非致病性大肠杆菌 ATCC 25922 和致病性大肠杆菌 O157:H7、O26:H11、O45:H2、O103:H11、O111、O121:H19 和 O145)的代谢多样性。基于两个有代表性的二维 H-C 图谱,在大肠杆菌细胞内样本中鉴定出 38 种代谢物。主成分分析表明,包括赖氨酸、精氨酸、α-酮戊二酸、腺苷和富马酸在内的代谢物是导致 ATCC 25922 大肠杆菌分离的原因。ATCC 25922 和致病性菌株之间的代谢差异较大。进一步分析了差异最大的两两分组(ATCC 25922 与 O26:H11)。筛选出的代谢物和富集途径测试表明,致病性菌株中的氨基酸代谢和能量产生要求更高。进一步测试了所选菌株的酸性反应。体外和体内失活动力学、形态变化和蛋白质渗漏表明,O26:H11 大肠杆菌具有更高的耐酸性。在酸性应激下对两种菌株的代谢分析揭示了两组中替代的代谢物和途径。致病性 O26:H11 的特点是更高的能量产生和氨基酸代谢(赖氨酸和谷氨酸)。实时 PCR 测试证实,谷氨酸依赖的脱羧酶/逆向转运蛋白系统是主要的耐酸机制。

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