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β-Dicarbonyls Facilitate Engineered Microbial Bromoform Biosynthesis

  • Thomas D. Loan
  • , Claudia E. Vickers
  • , Michael Ayliffe*
  • , Ming Luo*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Ruminant livestock produce around 24% of global anthropogenic methane emissions. Methanogenesis in the animal rumen is significantly inhibited by bromoform, which is abundant in seaweeds of the genus Asparagopsis. This has prompted the development of livestock feed additives based on Asparagopsis to mitigate methane emissions, although this approach alone is unlikely to satisfy global demand. Here we engineer a non-native biosynthesis pathway to produce bromoform in vivo with yeast as an alternative biological source that may enable sustainable, scalable production of bromoform by fermentation. β-dicarbonyl compounds with low pKa values were identified as essential substrates for bromoform production and enabled bromoform synthesis in engineered Saccharomyces cerevisiae expressing a vanadate-dependent haloperoxidase gene. In addition to providing a potential route to the sustainable biological production of bromoform at scale, this work advances the development of novel microbial biosynthetic pathways for halogenation.

Original languageEnglish
Pages (from-to)1492-1497
Number of pages6
JournalACS Synthetic Biology
Volume13
Issue number5
DOIs
Publication statusPublished - 17 May 2024
Externally publishedYes

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