Overexpression of Riboflavin Excretase Enhances Riboflavin Production in the Yeast Candida famata

Methods Mol Biol. 2021:2280:31-42. doi: 10.1007/978-1-0716-1286-6_3.

Abstract

Many microorganisms are capable of riboflavin oversynthesis and accumulation in a medium, suggesting that they efficiently excrete riboflavin. The mechanisms of riboflavin efflux in microorganisms remain elusive. Candida famata are representatives of a group of so-called flavinogenic yeast species that overproduce riboflavin (vitamin B2) in response to iron limitation. The riboflavin overproducers of this yeast species have been obtained by classical mutagenesis and metabolic engineering. Overproduced riboflavin accumulates in the cultural medium rather than in the cells suggesting existence of the special mechanisms involved in riboflavin excretion. The appropriate protein and gene have not been identified in yeasts till recently. At the same time, the gene BCRP (breast cancer resistance protein) has been identified in mammal mammary glands. Several homologs of the mammal BCRP gene encoding putative riboflavin efflux protein (excretase) were identified in the flavinogenic yeasts Debaryomyces hansenii and C. famata. Here we evaluate the yeast homologs of BCRP with respect to improvement of a riboflavin production by C. famata. The closest homologs from D. hansenii or C. famata were expressed under the control of TEF1 promoter of these yeasts in the wild-type and riboflavin-overproducing strains of C. famata. Resulted transformants overexpressed the corresponding genes (designated as DhRFE and CfRFE) and produced 1.4- to 6-fold more riboflavin as compared to the corresponding parental strains. They also were characterized by overexpression of RIB1 and RIB6 genes which encode the first and the last structural enzymes of riboflavin synthesis and exhibited elevated specific activity of GTP cyclohydrolase II. Thus, overexpression of yeast homolog of mammal gene BCRP may be useful to increase the riboflavin yield in a riboflavin production process using a recombinant overproducing C. famata strain or other flavinogenic microorganisms.

Keywords: BCRP (breast cancer resistance protein) gene; Candida famata yeast; Riboflavin biosynthesis; Riboflavin excretion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 2 / genetics*
  • Candida / genetics
  • Candida / growth & development*
  • Candida / metabolism
  • Cloning, Molecular
  • Culture Media / chemistry
  • Fungal Proteins / genetics
  • Gene Expression Regulation, Fungal
  • Metabolic Engineering / methods*
  • Peptide Elongation Factor 1 / genetics
  • Promoter Regions, Genetic
  • Riboflavin / biosynthesis*
  • Up-Regulation

Substances

  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • Culture Media
  • Fungal Proteins
  • Peptide Elongation Factor 1
  • Riboflavin