Metabolic responses to Lactobacillus plantarum contamination or bacteriophage treatment in Saccharomyces cerevisiae using a GC-MS-based metabolomics approach

被引:10
|
作者
Cui, Feng-Xia [1 ,2 ,3 ]
Zhang, Rui-Min [1 ]
Liu, Hua-Qing [1 ]
Wang, Yan-Feng [1 ]
Li, Hao [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Key Lab Bioproc, Coll Life Sci & Technol, Beijing 100029, Peoples R China
[2] Chinese Acad Med Sci, Inst Med Plant Dev, Beijing 100193, Peoples R China
[3] Peking Union Med Coll, Beijing 100193, Peoples R China
来源
关键词
Saccharomyces cerevisiae; Bioethanol; Bacteriophage; Lactobacillus plantarum contamination; Metabolomics; BACTERIAL-CONTAMINATION; ETHANOL TOLERANCE; HYDROGEN-PEROXIDE; YEAST; ACID; GROWTH; MEMBRANE; CHITOSAN; STRAINS;
D O I
10.1007/s11274-015-1949-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bacteriophage can be used as a potential alternative agent for controlling Lactobacillus plantarum contamination during bioethanol production. However, how Saccharomyces cerevisiae respond against contaminative L. plantarum or added bacteriophage remains to be fully understood. In this study, gas chromatography-mass spectrometry and a multivariate analysis were employed to investigate the intracellular biochemical changes in S. cerevisiae cells that were elicited by L. plantarum contamination or bacteriophage treatment. The intracellular metabolite profiles originating from different groups were unique and could be distinguished with the aid of principal component analysis. Moreover, partial least-squares-discriminant analysis revealed a group classification and pairwise discrimination, and 13 differential metabolites with variable importance in the projection value greater than 1 were identified. The metabolic relevance of these compounds in the response of S. cerevisiae to L. plantarum contamination or bacteriophage treatment was discussed. Besides generating lactic acid and competing for nutrients or living space, L. plantarum contamination might also inhibit the growth of S. cerevisiae through regulating the glycolysis in S. cerevisiae. Moreover, increased concentrations of monounsaturated fatty acids secondary to bacteriophage treatment might lead to more membrane fluidity and promote the cell viability of S. cerevisiae.
引用
收藏
页码:2003 / 2013
页数:11
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