Rapid Identification of γ-Butyrolactone Signalling Molecules in Diverse Actinomycetes Using Resin-Assisted Isolation and Chemoenzymatic Synthesis

26 December 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Actinomycetes are prolific producers of secondary metabolites with diverse chemical structures and bioactivities. Secondary metabolism in actinomycetes is regulated by signalling molecules, often termed “bacterial hormones.” In Streptomyces griseus, the γ-butyrolactone (GBL) A-factor (1) acts as a critical regulator of secondary metabolism, including antibiotic streptomycin production. The widespread presence of afsA, the gene encoding A-factor synthase, suggests that GBL compounds constitute a major class of signalling molecules in actinomycetes. However, the identification of GBLs has been limited by the requirement for large-scale actinomycete cultures. This study introduces two methodologies for the rapid identification of natural GBLs. First, a resin-assisted culture method combined with MS-guided screening enabled the isolation and structural determination of GBLs (2–5) from smaller-scale cultures. Second, a chemoenzymatic synthesis method for GBLs was developed, involving a one-pot system with three in vitro enzymatic reactions. Using isolated and synthesized GBLs (10a–10l), HR-LCMS analysis was conducted on 31 strains across 10 genera of actinomycetes. Synthesized GBLs were identified in nearly half of the tested strains, including genera where GBLs were detected for the first time. The absolute configurations of the GBLs were analysed using chiral HPLC, leading to the discovery of a (3S)-form GBL (11), an enantiomer of known GBLs. This study revealed the widespread distribution and structural diversity of GBLs among actinomycetes, providing insights into their regulatory roles and potential for activating secondary metabolism that support the discovery of new natural products.

Keywords

Actinomycete
LCMS
NMR
Structural determination
signalling molecule
chemoenzymatic synthesis
γ-butyrolactone

Supplementary materials

Title
Description
Actions
Title
Supplementary Information
Description
Experimental procedures, DNA and Protein Sequences, NMR data, LCMS chromatograms, MS spectra, CD spectra, chiral HPLC chromatograms and docking models.
Actions
Title
Supplementary Data
Description
NMR spectra of isolated natural products, synthesized substrates, and enzymatic products.
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.