Improving penicillin biosynthesis in Penicillium chrysogenum by glyoxalase overproduction

Christian Q. Scheckhuber, Marten Veenhuis, Ida J. van der Klei*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

6 Citations (Scopus)
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Abstract

Genetic engineering of fungal cell factories mainly focuses on manipulating enzymes of the product pathway or primary metabolism. However, despite the use of strong promoters or strains containing the genes of interest in multiple copies, the desired strongly enhanced enzyme levels are often not obtained.

Here we present a novel strategy to improve penicillin biosynthesis by Penicillium chrysogenum by reducing reactive and toxic metabolic by-products, 2-oxoaldehydes. This was achieved by overexpressing the genes encoding glyoxalase I and II, which resulted in a 10% increase in penicillin titers relative to the control strain.

The protein levels of two key enzymes of penicillin biosynthesis, isopenicillin N synthase and isopenicillin N acyltransferase, were increased in the glyoxalase transformants, whereas their transcript levels remained unaltered. These results suggest that directed intracellular reduction of 2-oxoaldehydes prolongs the functional lifetime of these enzymes. (C) 2013 Elsevier Inc. All rights reserved.

Original languageEnglish
Pages (from-to)36-43
Number of pages8
JournalMetabolic Engineering
Volume18
DOIs
Publication statusPublished - Jul-2013

Keywords

  • Glyoxalase
  • Glycation
  • Isopenicillin N synthase
  • Isopenicillin N acyltransferase
  • Methylglyoxal
  • 2-Oxoaldehyde
  • ISOPENICILLIN-N-SYNTHASE
  • PROTEIN
  • INVOLVEMENT
  • MODEL
  • GENE

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