Three genes encoding AfsK, AfsR, AfsS homologues in were studied, respectively, to investigate regulatory role of AfsKRS system for pristinamycin biosynthesis. Transcription change and gene inactivation analysis indicated that these genes had active transcription and positive regulation for the improvement of pristinamycin production in . The analysis of AfsKRS-defective mutagenesis indicated that there might be a positive correlation between the product of and pristinamycin I biosynthesis, and a negative correlation to pristinamycin II biosynthesis. However, both and might have negative correlation to pristinamycin I production and positive correlation to pristinamycin II production. The effects on pristinamycin production of AfsKRS disruptants by protein kinase inhibitor K252a indicated that AfsR, both not AfsK and AfsS, was the inhibition target of K252a in , and AfsR should serve as a pleiotropic regulator to have differential regulation on biosynthesis of pristinamycin I and II components. Based on above study, it might be deduced that different signal transduction patterns via AfsK, AfsR, AfsS of AfsKRS system should be involved in respective regulation for biosynthesis of pristinamycin I and II in . In conclusion, the investigation could give some valuable clues for exploring furtherly regulatory function of AfsKRS system in .
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http://dx.doi.org/10.1007/s13205-021-02933-2 | DOI Listing |
J Pharm Biomed Anal
December 2024
Research and Development Center, Zhejiang Medicine Co. Ltd., Shaoxing 312000, China. Electronic address:
The aim of this study was to develop and fully validate a sensitive and rapid ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for simultaneous quantification of pristinamycin ⅠA (PⅠA) and pristinamycin ⅡA (PⅡA) in plasma of beagle dogs after oral administration of pristinamycin tablets. PⅠA, PⅡA and quinupristin (internal standard, IS) were separated on an Agilent Eclipse Plus C column (2.1 mm × 100 mm, 3.
View Article and Find Full Text PDFJ Gen Appl Microbiol
September 2024
School of Biological and chemical Engineering, NingboTech University.
Prep Biochem Biotechnol
October 2022
Laboratoire Réactions et Génie des Procédés, UMR 7274, CNRS, Vandoeuvre Cedex, France.
Pristinamycin biosynthesis using and date sirup (DS) as substrates was optimized before scale-up. DS was filter sterilized as heat sterilization primes Maillard reactions having negative effects on antibiotic production. Multilinear regression modeling (MLR) predicted optimum medium composition, specifying components with positive and negative effects on production.
View Article and Find Full Text PDFEmerg Microbes Infect
December 2021
National Laboratory for Screening New Microbial Drugs, Institute of Medicinal Biotechnology, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
The emergence of drug-resistant tuberculosis (TB) constitutes a major challenge to TB control programmes. There is an urgent need to develop effective anti-TB drugs with novel mechanisms of action. Aspartate-semialdehyde dehydrogenase (ASADH) is the second enzyme in the aspartate metabolic pathway.
View Article and Find Full Text PDF3 Biotech
September 2021
School of Biological and Chemical Engineering, College of Innovation and Entrepreneurship, NingboTech University, Ningbo, 315100 China.
Three genes encoding AfsK, AfsR, AfsS homologues in were studied, respectively, to investigate regulatory role of AfsKRS system for pristinamycin biosynthesis. Transcription change and gene inactivation analysis indicated that these genes had active transcription and positive regulation for the improvement of pristinamycin production in . The analysis of AfsKRS-defective mutagenesis indicated that there might be a positive correlation between the product of and pristinamycin I biosynthesis, and a negative correlation to pristinamycin II biosynthesis.
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