Effects of S-adenosylmethionine on AfsKRS regulation in pristinamycin biosynthesis in Streptomyces pristinaespiralis

• Published in: Journal of general and applied microbiology Vol. 70; no. 2; p. 2024.03.002
• Main Authors: Jin, Qingchao, Wu, Zhige, Liu, Yan, Dong, Xinyan, Jin, Zhihua, Yang, Yu, Shen, Na
• Format: Journal Article
• Language: English
• Published: Japan Applied Microbiology, Molecular and Cellular Biosciences Research Foundation 01.01.2024; Japan Science and Technology Agency
• Subjects: AfsKRS system; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Biosynthesis; Gene Expression Regulation, Bacterial; Mutants; Mutation; Pristinamycin; Pristinamycin - biosynthesis; S-Adenosylmethionine; S-Adenosylmethionine - metabolism; Signal Transduction; Streptomyces; Streptomyces - genetics; Streptomyces - metabolism; Streptomyces pristinaespiralis; Streptomyces pristinaespiralis; pristinamycin; AfsKRS system; S-adenosylmethionine
• ISSN: 0022-1260; 1349-8037
• DOI: 10.2323/jgam.2024.03.002

In Streptomyces pristinaespiralis, AfsKRS system has differential regulation for PI and PII component biosynthesis of pristinamycin, but it is unknown whether S-adenosylmethionine (SAM) plays an important role in the AfsK-AfsR-AfsS signal transduction cascade during pristinamycin production. The possible target of exogenous SAM in the AfsKRS system and the biological role of SAM during the production of PI and PII were investigated using three mutantsΔafsK,ΔafsR andΔafsS defective in signal cascade pathway of AfsKRS. It was found that external SAM had a significant activation of PI production (1.85-fold increase) but had no obvious effect on PII production in the original strain F618 with the normal response of AfsKRS regulation. Addition of SAM resulted in a similar increase in pristinamycin yield in the mutant with defective afsK or afsR, but induced more crucial activation of PI biosynthesis than PII biosynthesis both in ΔafsK (1.65-fold and 1.15-fold increase respectively) and ΔafsR (1.27-fold and 1.09-fold increase respectively). Exogenous SAM only significantly enhanced PII production in ΔafsS (1.1-fold increase). These results could provide valuable insights into the regulatory function of the AfsKRS system in S. pristinaespiralis.