Bruinenberg P G, Evers M, Waterham H R, Kuipers J, Arnberg A C, AB G
Laboratory of Biochemistry, Groningen University, The Netherlands.
Biochim Biophys Acta. 1989 Jul 7;1008(2):157-67. doi: 10.1016/0167-4781(80)90003-2.
We have cloned the AMO gene, encoding the microbody matrix enzyme amine oxidase (EC 1.4.3.6) from the yeast Hansenula polymorpha. The gene was isolated by differential screening of a cDNA library, immunoselection, and subsequent screening of a H. polymorpha genomic library. The nucleotide sequence of a 3.6 kilobase stretch of DNA containing the amine oxidase (AMO) gene was determined. The AMO gene contains an open reading frame of 692 amino acids, with a relative molecular mass of 77,435. The 5' and 3' ends of the gene were mapped and show that the transcribed region measures 2134 nucleotides. The derived amino-acid sequence was confirmed by sequencing an internal proteolytic fragment of the purified protein. Amine oxidase contains the tripeptide sequence Ser-Arg-Leu, located 9 residues from the carboxy terminus, which may represent the topogenic signal for protein import into microbodies.
我们已经从多形汉逊酵母中克隆出了编码微体基质酶胺氧化酶(EC 1.4.3.6)的AMO基因。该基因是通过对cDNA文库进行差异筛选、免疫选择,随后对多形汉逊酵母基因组文库进行筛选而分离得到的。测定了包含胺氧化酶(AMO)基因的一段3.6千碱基DNA的核苷酸序列。AMO基因包含一个692个氨基酸的开放阅读框,相对分子质量为77435。对该基因的5'和3'末端进行了定位,结果表明转录区域长度为2134个核苷酸。通过对纯化蛋白的内部蛋白水解片段进行测序,证实了推导的氨基酸序列。胺氧化酶含有位于羧基末端9个残基处的三肽序列Ser-Arg-Leu,这可能代表了蛋白质导入微体的拓扑信号。