Genomic and transcriptomic analysis of genes involved in exopolysaccharide biosynthesis by Streptococcus thermophilus IMAU20561 grown on different sources of nitrogen

Exopolysaccharides (EPSs), which are produced by lactic acid bacteria, have been found to improve the texture and functionality of fermented dairy products. In a previous study, four nitrogen sources were identified as affecting the yield, molecular weight and structure of EPSs produced by IMAU20561...

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Veröffentlicht in:Frontiers in microbiology 2024-01, Vol.14, p.1328824-1328824
Hauptverfasser: Wang, Yuenan, Peng, Qingting, Liu, Yang, Wu, Na, He, Yanyan, Cui, Xinrui, Dan, Tong
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Sprache:eng
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Zusammenfassung:Exopolysaccharides (EPSs), which are produced by lactic acid bacteria, have been found to improve the texture and functionality of fermented dairy products. In a previous study, four nitrogen sources were identified as affecting the yield, molecular weight and structure of EPSs produced by IMAU20561 in M17 medium. In this genomic and transcriptomics study, a novel gene cluster responsible for assembly of repeating units of EPS is reported. This cluster (22.3 kb), consisting of 24 open reading frames, is located in the chromosomal DNA. To explore the biosynthetic mechanisms in EPS, we completed RNA-seq analysis of IMAU20561 grown in four different nitrogen sources for 5 h (log phase) or 10 h (stationary phase). GO functional annotation showed that there was a significant enrichment of differentially expressed genes (DEGs) involved in: amino acid biosynthesis and metabolism; ribonucleotide biosynthesis and metabolism; IMP biosynthesis and metabolism; and phosphorus metabolism. KEGG functional annotation also indicated enrichment of DEGs involved in amino acid biosynthesis, glycolysis, phosphotransferase system, fructose, and mannose metabolism. Our findings provide a better understanding the genetic traits of , the biosynthetic pathways needed for the production of EPS, and a theoretical basis for screening dairy starter cultures.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2023.1328824