Project name: Yarrowia lipolytica strain:W29

Description: Engineering a new metabolic function in a microbial host can be limited by the availability of the relevant co-factor. For instance, in Yarrowia lipolytica, the expression of a functional nitrate reductase is precluded by the absence of Molybdenum cofactor (Moco) biosynthesis. In this study, we demonstrated that the core Moco biosynthesis pathway from Ogataea parapolymorpha associated with the expression of a high affinity molybdate transporter could lead to the synthesis of Moco in Y. lipolytica. This was achieved by coupling Moco biosynthesis to the Moco-dependent nitrate assimilation pathway of the same donor O. parapolymorpha. In addition to 11 heterologous genes, fast growth on nitrate required adaptive laboratory evolution which, resulted in up to 100-fold increase in nitrate reductase activity and in up to 4-fold increase in growth rate. Genome sequencing of evolved isolates revealed the presence of a limited number of non-synonymous mutations or small insertions/deletions in annotated coding sequences. This study that builds up on a previous work establishing Moco synthesis in S. cerevisiae demonstrated that the Moco pathway could be successfully transferred in very distant yeasts and, potentially, to any other genera, which would enable the expression of new enzyme families and expand the nutrients range used by industrial yeasts.

Data type: raw sequence reads

Sample scope: Multiisolate

Relevance: Industrial

Last updated: 2021-02-25