Chaetoceros, the most
abundant genus
of marine planktonic diatoms, can be used in mariculture. An effective
genetic transformation system with a short transformation period was
established in Chaetoceros muelleri by electroporation in our previous study. In this study, a sequence-specific
clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9
vector applicable for C. muelleri was
constructed, and the expressions of sgRNA, resistance gene, and Cas9 gene were driven by the endogenous promoters U6, acetyl-CoA acetyltransferase, and fucoxanthin chlorophyll a/c binding protein, respectively,
in the vector. Nitrate reductase (NR) and urease (URE) genes were edited
in C. muelleri, and the NR knockout and NR/URE double-knockout
lines displayed the strict auxotrophic phenotype. In addition, the
DNA double-strand break was repaired by homologous recombination when
a donor DNA was introduced. CRISPR/Cas9 technology was successfully
applied to C. muelleri with an editing
efficiency of up to 86%, providing a molecular tool for the study
of basic biology in C. muelleri and
its synthetic biology applications.
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