Metabolomic and genomic insights into Micromonospora carbonacea subsp. caeruleus for anti-colorectal compound

Tepakorn Kongsaya1,2, Nuttaporn Emthomya1,2, Chananan Ngamcharungchit1,2

  • 1Department of Biotechnology, Faculty of Science, Mahidol University, Bangkok, 10400, Thailand.

Insights

A novel marine bacterium, Micromonospora carbonacea subsp. caeruleus 2MTK254, produces a potent anticancer compound. This polycyclic tetramate macrolactam (PTM) shows high efficacy against colorectal cancer cells, offering new therapeutic potential.

Area of Science:

  • Marine Microbiology
  • Natural Products Chemistry
  • Cancer Research

Background:

  • Marine Micromonospora species are recognized for their anticancer compound production.
  • Colorectal cancer remains a significant global health challenge, necessitating novel therapeutic strategies.

Purpose of the Study:

  • To isolate and characterize novel marine Micromonospora strains.
  • To identify and evaluate anticancer compounds from these isolates.
  • To conduct genomic and metabolomic analyses for compound discovery.

Main Methods:

  • Polyphasic taxonomic analysis of isolated strain 2MTK254.
  • Metabolomic analysis using molecular networking.
  • Genomic analysis to identify biosynthetic gene clusters (BGCs).
  • In vitro anticancer activity assays against colorectal cancer cell lines.

Main Results:

  • A novel subspecies, Micromonospora carbonacea subsp. caeruleus 2MTK254, was identified.
  • The strain's crude extract exhibited significant anti-colorectal activity (66.03% inhibition).
  • A novel polycyclic tetramate macrolactam (PTM), P1, demonstrated potent inhibition (99.31%) against HCT-116 cells (IC50 = 0.125 µM).
  • Genome analysis revealed unique PTM BGCs associated with compound P1.

Conclusions:

  • Micromonospora carbonacea subsp. caeruleus 2MTK254 is a promising source of novel PTMs.
  • The identified PTM exhibits significant anti-colorectal cancer potential.
  • Further investigation into these PTMs could lead to new cancer therapeutics.