Lin Xiaohua, Ke Chongrong, Wu Bisha, Zheng Yongbiao, Li Li, Chen Youqiang, Huang Jianzhong
Engineering Research Center of Industrial Microbiology, Ministry of Education, Fujian Normal University, Fuzhou 350108, China.
Sheng Wu Gong Cheng Xue Bao. 2011 Apr;27(4):572-8.
Construction and ethanol production effects of SNF4 gene knockout in Saccharomyces cerevisiae were described in this paper. For knockout of SNF4 gene in S. cerevisiae YS2, a PCR-amplified disruption cassette was used, encoding the short flanking homologous regions to the SNF4 gene and Kan(r) as selectable marker. The SNF4 gene disruption cassette was transformed into S. cerevisiae YS2 through LiAc/SS Carrier DNA/PEG. The positive transformants were grown on G418 plates and verified by PCR. The Kan(r) marker was rescued by transforming plasmid pSH65 into positive transformants and inducing expression of Cre recombinase in galactose-containing medium. Lastly, the YS2-deltaSNF4 strain, in which SNF4 allele gene were completely knocked out, was obtained by repeating the same procedure. The result of anaerobic fermentation showed that ethanol production of the SNF4 gene knockout strain had increased by 7.57 percent as compared with the original strain YS2. The experiment indicated ethanol production could be improved significantly with the approach ofSNF4 gene knockout by Cre-LoxP system.
本文描述了酿酒酵母中SNF4基因敲除的构建及其对乙醇生产的影响。为了敲除酿酒酵母YS2中的SNF4基因,使用了PCR扩增的破坏盒,其编码与SNF4基因短侧翼同源的区域以及作为选择标记的卡那霉素抗性基因(Kan(r))。通过醋酸锂/单链载体DNA/聚乙二醇(LiAc/SS Carrier DNA/PEG)将SNF4基因破坏盒转化到酿酒酵母YS2中。阳性转化子在G418平板上生长,并通过PCR进行验证。通过将质粒pSH65转化到阳性转化子中并在含半乳糖的培养基中诱导Cre重组酶的表达,去除了Kan(r)标记。最后,通过重复相同的程序获得了SNF4等位基因被完全敲除的YS2-ΔSNF4菌株。厌氧发酵结果表明,与原始菌株YS2相比,SNF4基因敲除菌株的乙醇产量提高了7.57%。该实验表明,通过Cre-LoxP系统敲除SNF4基因的方法可以显著提高乙醇产量。