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Engineering Flocculation for Improved Tolerance and Production of d-Lactic Acid in Pichia pastoris .

Kittapong Sae-TangPornsiri BumrungthamWuttichai MhuantongVerawat ChampredaSutipa TanapongpipatXin-Qing ZhaoChen-Guang LiuWeerawat Runguphan
Published in: Journal of fungi (Basel, Switzerland) (2023)
d-lactic acid, a chiral organic acid, can enhance the thermal stability of polylactic acid plastics. Microorganisms such as the yeast Pichia pastoris , which lack the natural ability to produce or accumulate high amounts of d-lactic acid, have been metabolically engineered to produce it in high titers. However, tolerance to d-lactic acid remains a challenge. In this study, we demonstrate that cell flocculation improves tolerance to d-lactic acid and increases d-lactic acid production in Pichia pastoris . By incorporating a flocculation gene from Saccharomyces cerevisiae ( ScFLO1 ) into P. pastoris KM71, we created a strain (KM71-ScFlo1) that demonstrated up to a 1.6-fold improvement in specific growth rate at high d-lactic acid concentrations. Furthermore, integrating a d-lactate dehydrogenase gene from Leuconostoc pseudomesenteroides ( Lp DLDH) into KM71-ScFlo1 resulted in an engineered strain (KM71-ScFlo1-LpDLDH) that could produce d-lactic acid at a titer of 5.12 ± 0.35 g/L in 48 h, a 2.6-fold improvement over the control strain lacking ScFLO1 expression. Transcriptomics analysis of this strain provided insights into the mechanism of increased tolerance to d-lactic acid, including the upregulations of genes involved in lactate transport and iron metabolism. Overall, our work represents an advancement in the efficient microbial production of d-lactic acid by manipulating yeast flocculation.
Keyphrases
  • lactic acid
  • saccharomyces cerevisiae
  • recombinant human
  • single cell
  • stem cells
  • microbial community
  • gene expression
  • dna methylation
  • poor prognosis
  • genome wide identification
  • copy number