Expansion of EasyClone-MarkerFree toolkit for Saccharomyces cerevisiae genome with new integration sites

被引:16
作者
Babaei, Mahsa [1 ]
Sartori, Luisa [1 ]
Karpukhin, Alexey [2 ]
Abashkin, Dmitrii [2 ]
Matrosova, Elena [2 ]
Borodina, Irina [1 ]
机构
[1] Tech Univ Denmark, Novo Nordisk Fdn Ctr Biosustainabil, Kemitorvet Bldg 220, DK-2800 Lyngby, Denmark
[2] Ajinomoto Genet Res Inst, Moscow, Russia
关键词
chromosomal integration; CRISPR-Cas9; genome editing; metabolic engineering; CHROMOSOMAL INTEGRATION; EXPRESSION; GENES;
D O I
10.1093/femsyr/foab027
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biotechnological production requires genetically stable recombinant strains. To ensure genomic stability, recombinant DNA is commonly integrated into the genome of the host strain. Multiple genetic tools have been developed for genomic integration into baker's yeast Saccharomyces cerevisiae. Previously, we had developed a vector toolkit EasyClone-MarkerFree for stable integration into eleven sites on chromosomes X, XI, and XII of S. cerevisiae. The markerless integration was enabled by CRISPR-Cas9 system. In this study, we have expanded the kit with eight additional intergenic integration sites located on different chromosomes. The integration efficiency into the new sites was above 80%. The expression level of green fluorescence protein (gfp) for all eight sites was similar or above XI-2 site from the original EasyClone-MarkerFree toolkit. The cellular growth was not affected by the integration into any of the new eight locations. The eight-vector expansion kit is available from AddGene.
引用
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页数:6
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