AI Article Synopsis

  • Aspergillus terreus is recognized for producing important substances like lovastatin and itaconic acid, and researchers aim to enhance their production through genetic engineering.
  • A whole genome sequence of A. terreus ATCC 20541 reveals 10,410 predicted protein-coding genes and highlights unique genetic features, including a specific lovastatin biosynthetic gene cluster only found in this strain.
  • The study analyzes the diversity of carbohydrate-active enzymes (CAZymes), cytochrome P450s (CYPs), and secondary metabolites across eleven A. terreus strains, showing distinct patterns that could guide future research on beneficial secondary metabolites and their gene clusters.

Article Abstract

Aspergillus terreus is well-known for lovastatin and itaconic acid production with biomedical and commercial importance. The mechanisms of metabolite formation have been extensively studied to improve their yield through genetic engineering. However, the combined repertoire of carbohydrate-active enzymes (CAZymes), cytochrome P450s (CYP) enzymes, and secondary metabolites (SMs) in the different A. terreus strains has not been well studied yet, especially with respect to the presence of biosynthetic gene clusters (BGCs). Here we present a 30 Mb whole genome sequence of A. terreus ATCC 20541 in which we predicted 10,410 protein-coding genes. We compared the CAZymes, CYPs enzyme, and SMs across eleven A. terreus strains, and the results indicate that all strains have rich pectin degradation enzyme and CYP52 families. The lovastatin BGC of lovI was linked with lovF in A. terreus ATCC 20541, and the phenomenon was not found in the other strains. A. terreus ATCC 20541 lacked a non-ribosomal peptide synthetase (AnaPS) participating in acetylaszonalenin production, which was a conserved protein in the ten other strains. Our results present a comprehensive analysis of CAZymes, CYPs enzyme, and SM diversities in A. terreus strains and will facilitate further research in the function of BGCs associated with valuable SMs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814666PMC
http://dx.doi.org/10.1038/s41598-022-27311-7DOI Listing

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