Cordero Otero R, Gaillardin C
Laboratoire de Génétique Moléculaire et Cellulaire INRA-CNRS, Institut National Agronomique Paris-Grignon, Centre de Biotechnologies Agro Industrielles, Thiverval-Grignon, France.
Appl Microbiol Biotechnol. 1996 Sep;46(2):143-8. doi: 10.1007/s002530050796.
The yeast Yarrowia lipolytica was shown to be sensitive to the aminoglycoside antibiotic hygromycin B. Spontaneous resistants appeared at a frequency of (2-5) x 10(-7) in media containing 100 mg/l drug. In order to develop a new selective marker for the transformation of this yeast, we constructed new plasmids expressing the Escherichia coli hygromycin-resistance gene (hph) under the control of the promoter and terminator sequences of the strongly expressed XPR2 gene of Y. lipolytica. Direct selection of hygromycin-B-resistant transformants on complete medium was very efficient and resulted in transformation frequencies comparable to those observed with conventional auxotrophic markers. This new marker can be used for integrating single copies of plasmid and for gene disruption and provides a convenient tag for genetic studies.
已证明解脂耶氏酵母对氨基糖苷类抗生素潮霉素B敏感。在含有100 mg/l该药物的培养基中,自发抗性出现的频率为(2 - 5)×10(-7)。为了开发一种用于该酵母转化的新选择标记,我们构建了新质粒,其在解脂耶氏酵母强表达的XPR2基因的启动子和终止子序列控制下表达大肠杆菌潮霉素抗性基因(hph)。在完全培养基上直接选择潮霉素B抗性转化体非常有效,其转化频率与使用传统营养缺陷型标记所观察到的频率相当。这种新标记可用于整合质粒单拷贝和基因敲除,并为遗传研究提供了一个方便的标签。