摘要
通过对黑曲霉N2 5植酸酶phyA基因PCR扩增 ,获得了一条长约 1 6kb的特异性PCR产物 ,并进行了酶切鉴定。然后在pUC1 8质粒中构建了含有目的基因片段的克隆质粒pFNP 1。DNA序列测定表明 ,目的基因片段含有植酸酶phyA基因的完整序列 ,phyA基因全长1 50 6bp,其中包含一段长 1 0 2bp的内含子 ,编码 467个氨基酸 ,5’端有一段编码 1 9个氨基酸的信号肽序列。黑曲霉N2 5与产植酸酶酶活最高的天然黑曲霉标准菌株NRRL31 35的植酸酶phyA基因 (GenBankAccession :M94550 )相比较 ,其同源性为 96 746% ,编码的氨基酸序列同源性为 97 64%。将黑曲霉N2 5植酸酶phyA基因序列及其相应的氨基酸序列在国际基因库中注册 (注册号分别为 :AF2 1 881 3,AAF2 5481 1 ) ,此基因是目前中国在国际基因库中注册的第一个植酸酶phyA基因。
The phyA encoding phytase of Aspergillus niger N25 was amplified by the polymerase chain reaction (PCR) with primers designed according to the sequences of the phyA in GenBank.The amplified fragment was cloned and sequenced.The results show that:the coding region is 1506bp in size,includes a 102bp intron,and encodes a peptide of 476 amino acid residues,in which there is a signal peptide with 19 amino acids and a mature peptide of 448 amino acids.Comparison of this sequence with the phyA of the natural A.niger NRRL3135 (GenBank Accession:M94550),the most highly secreting\|phytase strain,shows that the nucleotide homology is as high as 96.746%,and the amino acid homology comes up to 97.64%.The phyA of A.niger N25 strain in this paper is appropriate to be used to construct the phytase gene\|engineering bacteria.The phyA and its amino acid sequence have been accessed by GenBank (Accession:AF218813,AAF25481.1).
出处
《微生物学报》
CAS
CSCD
北大核心
2001年第3期310-314,共5页
Acta Microbiologica Sinica
基金
"九五"国家重点科技攻关项目 ( 96 0 0 9 0 2 0 6)&&
