摘要
参考Hartingsveldt已发表的NRRL3135植酸酶 (phyA)基因序列 ,设计并合成了一对引物 ,应用PCR技术 ,以土曲霉CCTCCAF 930 44总DNA为模板 ,扩增出了不包括假定的信号肽序列的phyA基因 ,并将其克隆到PMD18-T载体上 ,测定了其核苷酸序列 ,并推导了其氨基酸序列 .该基因全长为 1433bp ,与已发表的NRRL3135的phyA基因的同源性为 97% ,编码一个含 45
Phytase catalyzes the hydrolysis of phytate(myo-inositol hexakisphosphate)to phosphate and myo-inositol, thereby improving the bioavailability of phytate phosphorus in plant foods and reducing phosphorus pollution of animal waste. A phytase gene from the A.terrus strain CCTCC 93044 was cloned by PCR and sequenced. The PCR primers were designed based on the published sequence of NRRL 3135 phyA. The phytase gene we cloned comprises 1 433 nucleotides without the putative signal sequence and encodes a polypeptide of 458 amino acids. The phytase gene shows 97% identity to the NRRL 3135 PhyA. It was planned to express this gene in yeast.
出处
《湖北大学学报(自然科学版)》
CAS
2001年第2期174-177,共4页
Journal of Hubei University:Natural Science