Metzger M H, Hollenberg C P
Institut für Mikrobiologie, Heinrich-Heine-Universität, Düsseldorf, Germany.
Appl Microbiol Biotechnol. 1994 Nov;42(2-3):319-25. doi: 10.1007/BF00902736.
The gene TKT from P. stipitis, encoding the enzyme transketolase (EC 2.2.1.1), was cloned from a genomic library by hybridization with a S. cerevisiae TKT1-gene-specific probe. The nucleotide sequence determined contains an open-reading frame of 2085 base pairs (bp) encoding a protein of 695 amino acids with a predicted molecular mass of 75113 Da. The TKT gene was actively expressed in S. cerevisiae when placed under the control of the homologous PDC1(-15) promoter and could complement a S. cerevisiae tkt deletion. The TKT protein was immunologically detectable using S. cerevisiae transketolase-specific antiserum. Overexpression of the P. stipitis TKT gene in a xylose-utilizing S. cerevisiae XYL1/XYL2 integrant led to a drastically extended generation time during growth on xylose minimal medium under aerobic conditions.
来自树干毕赤酵母的编码转酮醇酶(EC 2.2.1.1)的TKT基因,通过与酿酒酵母TKT1基因特异性探针杂交,从基因组文库中克隆得到。测定的核苷酸序列包含一个2085个碱基对(bp)的开放阅读框,编码一个695个氨基酸的蛋白质,预测分子量为75113 Da。当TKT基因置于同源PDC1(-15)启动子的控制下时,它在酿酒酵母中能活跃表达,并且可以互补酿酒酵母tkt缺失。使用酿酒酵母转酮醇酶特异性抗血清可通过免疫检测到TKT蛋白。树干毕赤酵母TKT基因在利用木糖的酿酒酵母XYL1/XYL2整合体中的过表达,导致在有氧条件下于木糖基本培养基上生长期间的代时大幅延长。