Kirimura K, Yoda M, Usami S
Department of Applied Chemistry, School of Science and Engineering, Waseda University, Ohkubo 3-4-1, Shinjuku-ku, Tokyo 169-8555, Japan.
Curr Genet. 1999 Jan;34(6):472-7. doi: 10.1007/s002940050422.
A cDNA fragment encoding the mitochondrial alternative oxidase, the enzyme responsible for cyanide-insensitive and salicylhydroxamic acid (SHAM)-sensitive respiration, from the citric acid-producing fungus Aspergillus niger WU-2223L was cloned and expressed in Escherichia coli as a host strain. Synthetic primers were designed from the conserved nucleotide sequences of the alternative oxidase genes from higher plants and a yeast. The 210-bp DNA fragment was amplified by PCR with these primers using chromosomal DNA of WU-2223L as a template, and was employed to screen a cDNA library of A. niger. One full-length cDNA clone of 1.2 kb was obtained, and was sequenced to reveal that the clone contained an open reading frame (ORF-AOX1) encoding a polypeptide of 351 amino acids. The predicted amino-acid sequence exhibited 50%, 55%, and 52% homology to the alternative oxidases of Hansenula anomala, Neurospora crassa and Sauromatum guttatum, respectively. In the 5'-terminus region of the ORF-AOX1, a mitochondrial targeting motif was found. The whole open reading frame of ORF-AOX1 was ligated to plasmid pKK223-3 to construct the expression vector pKAOX1. The E. coli transformant harboring pKAOX1 showed cyanide-insensitive and SHAM-sensitive respiration, and expression was increased approximately two-fold by the addition of IPTG. These results indicated that the ORF-AOX1 encodes an alternative oxidase of A. niger.
从柠檬酸生产真菌黑曲霉WU-2223L中克隆出一个编码线粒体交替氧化酶的cDNA片段,该酶负责氰化物不敏感和水杨羟肟酸(SHAM)敏感的呼吸作用,并在大肠杆菌宿主菌株中进行表达。根据高等植物和酵母交替氧化酶基因的保守核苷酸序列设计合成引物。以WU-2223L的染色体DNA为模板,用这些引物通过PCR扩增出210bp的DNA片段,并用于筛选黑曲霉的cDNA文库。获得了一个1.2kb的全长cDNA克隆,并对其进行测序,结果显示该克隆包含一个编码351个氨基酸多肽的开放阅读框(ORF-AOX1)。预测的氨基酸序列与异常汉逊酵母、粗糙脉孢菌和斑龙芋的交替氧化酶分别具有50%、55%和52%的同源性。在ORF-AOX1的5'末端区域,发现了一个线粒体靶向基序。将ORF-AOX1的整个开放阅读框连接到质粒pKK223-3上,构建表达载体pKAOX1。携带pKAOX1的大肠杆菌转化体表现出氰化物不敏感和SHAM敏感的呼吸作用,添加IPTG后表达量增加约两倍。这些结果表明ORF-AOX1编码黑曲霉的一种交替氧化酶。