4.7 Article

Analyses of plantaricin Q7 synthesis by Lactobacillus plantarum Q7 based on comparative transcriptomics

期刊

FOOD CONTROL
卷 124, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.foodcont.2021.107909

关键词

L; plantarum Q7; Plantaricin Q7; Synthesis; Transcriptome; Heat shock protein; Induction

资金

  1. National Natural Science Foundation of China [31771988]
  2. Key program of Natural Science Foundation of Shandong province in China [ZR2020KC009]
  3. advantageous and characteristic discipline program of Heilongjiang Province in China [4]

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Plantaricin Q7, a bacteriocin with broad-spectrum antibacterial activity produced by Lactobacillus plantarum Q7, has shown low yield as the main obstacle to industrialization. Transcriptomics analysis revealed critical time points in Plantaricin Q7 synthesis, with key genes encoding ABC transporters, histidine protein kinase, and heat shock proteins playing crucial roles. Environmental induction, particularly with 2% NaCl, increased Plantaricin Q7 production by 33.33%, highlighting the potential importance of the groS gene in synthesis enhancement.
Plantaricin Q7 was a bacteriocin with broad-spectrum antibacterial activity and biosafety produced by Lactobacillus plantarum Q7. However, the low yield of plantaricin Q7 was the main limitation to its industrialization. To understand the plantaricin Q7 production at the level of transcription, the biosynthesis of plantaricin Q7 from L. plantarum Q7 was investigated by transcriptomics. It was found that there were four critical time points in plantaricin Q7 synthesis stage. Plantaricin Q7 entered the synthesis period at 2 h, and the largest synthesis rate was observed at 6 h. The highest production of plantaricin Q7 reached at 12 h, and the production began to decrease at 16 h. The transcriptomics results of GO function and KEGG pathway analyses at those four time points showed that oppD encoding ABC oligopeptide transporter, pedC encoding bacteriocin ABC transport accessory protein, agrC encoding histidine protein kinase, and groL as well as groS encoding heat shock protein and accessory protein played a key role in the synthesis of plantaricin Q7. In addition, clpL and clpP encoding protease could cause the degradation of plantaricin Q7. When environmental induction was used to regulate the express of the heat shock protein, plantaricin Q7 yield was increased by 33.33% when 2% NaCl as inducer, and groS was significantly up-regulated. It was suggested that groS could be a critical gene for the synthesis of plantaricin Q7. These findings provided new regulated targets to improve the production of bacteriocins.

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