Establishment of a transgene expression system for the marine microalga Schizochytrium by 18S rDNA-targeted homologous recombination

Schizochytrium is an established candidate for commercial production of long chain polyunsaturated fatty acids (PUFAs) that are important in human health and aquaculture. Genetic engineering technology has been applied successfully to increase the metabolites in many organisms. In order to use genetic engineering technology to enhance lipid accumulation in Schizochytrium for economically feasible PUFAs production, the transgene expression system should be established first. In the present study, we investigated a novel transgene expression system in Schizochytrium by 18S rDNA-targeted homologous recombination. The targeting vector pBS-18S-ZeoR contains a portion of 18S rDNA from Schizochytrium and the Zeocin resistance gene (Streptoalloteichus hindustanus bleomycin gene, Sh ble gene) expression cassette. This targeting vector was transformed into Schizochytrium by electroporation and the transformants were then selected on Zeocin-containing plates. The exogenous Sh ble gene has been incorporated into the genome of Schizochytrium according to PCR amplification. More importantly, the majority of the transformants showed similar biomass and total lipid to the wild type strain. Our results suggest that the 18S rDNA is a suitable recombination site and this system could be used to introduce new functional genes into Schizochytrium.