Nicolaisen M, Frisvad J C, Rossen L
Biotechnological Institute, Technical University of Denmark, Lyngby, Denmark.
Lett Appl Microbiol. 1997 Sep;25(3):197-201. doi: 10.1046/j.1472-765x.1997.00005.x.
A Penicillium freii DNA fragment with similarity to the beta-keto-acyl synthase motif of the P. griseofulvum 6-methylsalicylic acid synthase encoding gene (MSAS) was identified by screening a cosmid library using a part of MSAS as the probe. Two exons of 93 and 849 bp, encoding a predicted polypeptide of 314 amino acids, and a molecular mass of 33.4 kDa, were identified (PfKS). PfKS was transcribed as a 1.6 kbp messenger. A region corresponding to the MSAS gene encoding essential enzyme activities for the assembly of a polyketide chain was absent in PfKS. Gene disruption experiments in P. freii with a truncated version of PfKS did not result in the detection of homologous integration events.
通过使用灰黄青霉6-甲基水杨酸合酶编码基因(MSAS)的一部分作为探针筛选黏粒文库,鉴定出了一个与灰黄青霉MSAS的β-酮酰基合酶基序具有相似性的弗氏青霉DNA片段。鉴定出了两个外显子,分别为93 bp和849 bp,编码一个预测的314个氨基酸的多肽,分子量为33.4 kDa(PfKS)。PfKS转录为一个1.6 kbp的信使RNA。PfKS中不存在与编码聚酮链组装必需酶活性的MSAS基因相对应的区域。用截短版本的PfKS对弗氏青霉进行基因破坏实验,未检测到同源整合事件。