MCR1 participates in:
Ergosterol biosynthesis: Electron transfer to cytochrome b5 for sterol desaturation .
Oxidative stress response: Overexpression enhances resistance to hydrolysate inhibitors (e.g., furfural) by accelerating furaldehyde reduction .
Fatty acid metabolism: Supports PUFA biosynthesis in M. alpina via NADH-dependent electron transport .
Expression systems: Successfully expressed in E. coli (limited solubility) and Pichia pastoris .
Purification methods:
Biotechnological applications: Engineered S. cerevisiae strains with MCR1 overexpression show improved ethanol production rates in lignocellulose hydrolysates .
Mitochondrial dynamics: Incomplete outer membrane arrest sorts MCR1 to dual submitochondrial compartments, suggesting regulatory crosstalk between translocation machineries .
No direct studies on Candida albicans MCR1 exist in the reviewed literature. Current insights derive from homologous systems, highlighting the need for C. albicans-specific investigations to resolve its role in pathogenicity or antifungal resistance.
KEGG: cal:CAALFM_C602040WA