Litcius/Paper detail

Deletion of Plasma Membrane Malate Transporters Increased Lipid Accumulation in the Oleaginous Fungus <i>Mucor circinelloides</i> WJ11

Junhuan Yang, José Tomás Cánovas-Márquez, Pengcheng Li, Shaoqi Li, Junchao Niu, Xiuwen Wang, Yusuf Nazir, Sergio López‐García, Victoriano Garre, Yuanda Song

2021Journal of Agricultural and Food Chemistry24 citationsDOI

Abstract

Malate as an important intermediate metabolite, its subcellular location, and concentration have a significant impact on fungal lipid metabolism. Previous studies showed that the mitochondrial malate transporter plays an important role in lipid accumulation in Mucor circinelloides by manipulating intracellular malate concentration. However, the role of plasma membrane malate transporters in oleaginous fungi remains unexplored. Therefore, in this work, two plasma membrane malate transporters “2-oxoglutarate:malate antiporters” (named SoDIT-a and SoDIT-b) of M. circinelloides WJ11 were deleted, and the consequences in growth capacity, lipid accumulation, and metabolism were analyzed. The results showed that deletion of sodit-a or/and sodit-b reduced the extracellular malate, confirming that the products of both genes participate in malate transportation. In parallel, the lipid contents in mutants increased approximately 10–40% higher than that in the control strain, suggesting that the defect in plasma membrane malate transport results in an increase of malate available for lipid biosynthesis. Furthermore, transcriptional analysis showed that the expression levels of multiple key genes involved in the lipid biosynthesis were also increased in the knockout mutants. To the best of our knowledge, this is the first report that demonstrated the association between plasma membrane malate transporters and lipid accumulation in M. circinelloides.

Topics & Concepts

Mucor circinelloidesFungusTransporterMucorBiologyChemistryBiochemistryFilamentous fungusBotanyEnzymeGeneAspergillusMicrobial Metabolic Engineering and BioproductionEnzyme Catalysis and ImmobilizationMitochondrial Function and Pathology