Schweizer M, Case M E, Dykstra C C, Giles N H, Kushner S R
Gene. 1981 Jun-Jul;14(1-2):23-32. doi: 10.1016/0378-1119(81)90145-1.
A 22.2-kb insert of Neurospora crassa DNA containing at least two of the genes from the inducible catabolic quinic acid pathway has been cloned into the cosmid vehicle pHC79 resulting in a recombinant plasmid, pMSK308. The qa-2+ locus (which encodes catabolic dehydroquinase) is functionally expressed in both Escherichia coli and qa-2 mutants of N. crassa transformed with pMSK308 plasmid DNA. Expression of the qa-3 gene (which encodes quinate dehydrogenase) is only detected upon reintroduction into N. crassa. Results were also obtained which suggested that the qa-4 gene, which maps between qa-2 and qa-3, may also be present on both pMSK308 and the previously described plasmid pVK88. Certain anomalies in the types of N. crassa transformants obtained with pMSK308 plasmid DNA were noted.
一段含有来自可诱导分解代谢奎尼酸途径至少两个基因的22.2 kb粗糙脉孢菌DNA片段已被克隆到黏粒载体pHC79中,得到重组质粒pMSK308。qa - 2 +基因座(编码分解代谢脱氢奎尼酸酶)在用pMSK308质粒DNA转化的大肠杆菌和粗糙脉孢菌的qa - 2突变体中均有功能表达。qa - 3基因(编码奎尼酸脱氢酶)的表达仅在重新导入粗糙脉孢菌后才能检测到。还获得了结果表明,位于qa - 2和qa - 3之间的qa - 4基因可能也存在于pMSK308和先前描述的质粒pVK88上。注意到用pMSK308质粒DNA获得的粗糙脉孢菌转化体类型存在某些异常。