4.4 Article

Effects of tryptophan and phenylalanine on tryptophol production in Saccharomyces cerevisiae revealed by transcriptomic and metabolomic analyses

Journal

JOURNAL OF MICROBIOLOGY
Volume 60, Issue 8, Pages 832-842

Publisher

MICROBIOLOGICAL SOCIETY KOREA
DOI: 10.1007/s12275-022-2059-2

Keywords

Saccharomyces cerevisiae; tryptophol production; multiomic analysis; nitrogen catabolite repression; thiamine regulon gene thi4; transamination and decarboxylation

Categories

Funding

  1. National Natural Science Foundation of China [32060531, 31660451]
  2. Yunnan Fundamental Research Project [202101AT070279]
  3. Research Foundation for Advanced Talents of Jiangxi Normal University
  4. Key Scientific Research Project of China Tobacco Yunnan Industrial Co., Ltd. [2020XY01]

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The study found that tryptophan significantly promoted the production of tryptophol (TOL), but the output plateaued at a certain concentration, while phenylalanine reduced the stimulating effect of tryptophan. The effects of these two amino acids on TOL production were related to the transamination and decarboxylation of the Ehrlich pathway.
Tryptophol (TOL) is a metabolic derivative of tryptophan (Trp) and shows pleiotropic effects in humans, plants and microbes. In this study, the effect of Trp and phenylalanine (Phe) on TOL production in Saccharomyces cerevisiae was determined, and a systematic interpretation of TOL accumulation was offered by transcriptomic and metabolomic analyses. Trp significantly promoted TOL production, but the output plateaued (231.02-266.31 mg/L) at Trp concentrations >= 0.6 g/L. In contrast, Phe reduced the stimulatory effect of Trp, which was strongly dependent on the Phe concentration. An integrated genomic, transcriptomic, and metabolomic analysis revealed that the effect of Trp and Phe on TOL production was mainly related to the transamination and decarboxylation of the Ehrlich pathway. Additionally, other genes, including thiamine regulon genes (this), the allantoin catabolic genes dal1, dal2, dal4, and the transcriptional activator gene aro80, may play important roles. These findings were partly supported by the fact that the thi4 gene was involved in TOL production, as shown by heterologous expression analysis. To the best of our knowledge, this novel biological function of thi4 in S. cerevisiae is reported here for the first time. Overall, our findings provide insights into the mechanism of TOL production, which will contribute to TOL production using metabolic engineering strategies.

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