【摘要】 为寻找高效低毒的抗真菌药物,利用PCR技术扩增了编码人嗜铬粒蛋白N端18-76、18-66和31-76位氨基酸(CGA18-76、CGA18-66和CGA31-76)的DNA片段,将之克隆进枯草杆菌诱导型表达载体pSBPTQ,获得3种重组质粒pSC18-76、pSC18-66和pSC31-76,转化枯草杆菌DB1342。SDS-PAGE分析结果显示:经蔗糖诱导后,CGA18-76、CGA18-66和CGA31-76片段分别在枯草杆菌工程菌中获得表达,产物分泌到细胞外。表达量分别为5.6 mg/L、5.3 mg/L和5.6 mg/L。利用孔穴琼脂扩散法检测表达产物的抗真菌活性,并与CGA1-76进行比较,发现CGA18-76、CGA18-66和CGA31-76对烟曲霉菌、黄曲霉菌、石膏样小孢子菌和白念珠菌均有抑制作用,并以CGA31-76对白念珠菌的抑制作用为最强,CGA18-66对除白念珠菌之外的另3种测试真菌的抑制作用较强,而CGA18-76对测试真菌的抑制作用最弱。更多还原

【Abstract】 To find antifungal compounds with low toxicity to mammalian cells,the DNA fragments encoding the N terminal 18-76,18-66,and 31-76 amino acid sequences(CGA18-76,CGA18-66,and CGA31-76) of human CGA were amplified by PCR technique.The amplified DNA fragments were cloned into the Bacillus subtilis inducible expression vector pSBPTQ and the resultant plasmids pSC18-76,pSC18-66,and pSC31-76 were then transformed into B.subtilis strain DB1342 competent cells respectively.SDS-PAGE results showed that CGA18-76,CGA18-66 and CGA31-76 were expressed by sucrose induction and secreted into the medium with a yield of 5.6 mg/L, 5.3 mg/L and 5.6 mg/L respectively.The antifungal activity of the expressed products was examined and compared with CGA1-76.The results demonstrate that all four fragments CGA1-76,GA18-76,CGA18-66 and CGA31-76 inhibit the growth of A.fumigatus,A.flavus,M.gypseum and C.albican,while CGA31-76 has the highest inhibition activity specifically on C.albican,and CGA18-66 shows the strongest inhibition on these fungi except C.albican,and CGA18-76 shows the weakest inhibition on these fungi.更多还原