3.9 Article

Itaconic acid production is regulated by LaeA in Aspergillus pseudoterreus

期刊

出版社

ELSEVIER
DOI: 10.1016/j.mec.2022.e00203

关键词

Aspergillus pseudoterreus; Itaconic acid; laeA Process robustness; Multi-omics; Phosphate

资金

  1. U.S. Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy (EERE), Bioenergy Technologies Office (BETO) [DE-NL0030038]
  2. Office of Biological and Environmental Research [grid.436923.9]
  3. DOE [DE-AC05-76RLO 1830]
  4. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]

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The global regulator LaeA plays a crucial role in controlling secondary metabolism in diverse Aspergillus species. This study reveals its importance in regulating itaconic acid production in Aspergillus pseudoterreus. Overexpression of LaeA enhances itaconic acid yield by increasing the expression of key biosynthetic pathway enzymes and attenuating the expression of genes involved in phosphate acquisition and scavenging.
The global regulator LaeA controls secondary metabolism in diverse Aspergillus species. Here we explored its role in regulation of itaconic acid production in Aspergillus pseudoterreus. To understand its role in regulating metabolism, we deleted and overexpressed laeA, and assessed the transcriptome, proteome, and secreted metabolome prior to and during initiation of phosphate limitation induced itaconic acid production. We found that secondary metabolite clusters, including the itaconic acid biosynthetic gene cluster, are regulated by laeA and that laeA is required for high yield production of itaconic acid. Overexpression of LaeA improves itaconic acid yield at the expense of biomass by increasing the expression of key biosynthetic pathway enzymes and attenuating the expression of genes involved in phosphate acquisition and scavenging. Increased yield was observed in optimized conditions as well as conditions containing excess nutrients that may be present in inexpensive sugar containing feedstocks such as excess phosphate or complex nutrient sources. This suggests that global regulators of metabolism may be useful targets for engineering metabolic flux that is robust to environmental heterogeneity.

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