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克隆油菜GDSL脂肪酶基因BnLIP1,实现该基因在原核系统中重组表达,为研究其功能奠定基础。采用TRIzol法提取总RNA,通过RT-PCR法扩增BnLIP1编码序列,构建原核表达载体pEL1并转化大肠杆菌,IPTG诱导表达后通过SDS-PAGE检测目的蛋白。根据GenBank报道的序列设计引物,从萌发的油菜种子黄化幼苗中成功克隆到BnLIP1的编码序列,长度为1170bp。将该编码序列构建到原核表达载体pET32a( )并与标签序列融合,在E.coliBL21菌株中成功表达了与标签蛋白融合的BnLIP1蛋白,大小约为61kDa。首次实现了油菜GDSL脂肪酶基因在原核系统中的表达,为GDSL脂肪酶Bn-LIP1蛋白的分离纯化及活性研究奠定了基础。 相似文献
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克隆油菜GDSL脂肪酶基因BnLIP1,实现该基因在原核系统中重组表达,为研究其功能奠定基础。采用TRIzol法提取总RNA,通过RT-PCR法扩增BnLIP1编码序列,构建原核表达载体pEL1并转化大肠杆菌,IPTG诱导表达后通过SDS-PAGE检测目的蛋白。根据GenBank报道的序列设计引物,从萌发的油菜种子黄化幼苗中成功克隆到BnLIP1的编码序列,长度为1170bp。将该编码序列构建到原核表达载体pET32a( )并与标签序列融合,在E.coliBL21菌株中成功表达了与标签蛋白融合的BnLIP1蛋白,大小约为61kDa。首次实现了油菜GDSL脂肪酶基因在原核系统中的表达,为GDSL脂肪酶Bn-LIP1蛋白的分离纯化及活性研究奠定了基础。 相似文献
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A major esterase (designated OsEST1) showing high activity using 1-naphthyl acetate as a substrate was identified from rice bran and purified approximately 239-fold to near-homogeniety. The purified enzyme migrated as a single polypeptide band on native and SDS-polyacrylamide gels and had a molecular mass of 25 kDa under denaturing conditions. Analysis of its tryptic peptides by MALDI-TOF-MS and subsequent data mining identified a corresponding cDNA OsEST1 consisting of 714 nucleotides and encoding a 238 amino acid protein. Analysis of its primary sequence indicated that OsEST1 is a GDSL-motif carboxylester hydrolase belonging to the SGNH protein subfamily in containing the putative catalytic triad of Ser11, Asp187, and His190. OsEST1 showed the highest catalytic activity at approximately pH 8.0–8.5 and at 45 °C with Km and Vmax values for 1-naphthyl acetate of 172 μM and 63.7 μmol/min/mg protein, respectively. However, OsEST1 showed no activity with triacylglycerol. Alignment of the primary sequence of OsEST1 and other rice GDSL-motif esterases/lipases showed that OsEST1 aligns with a specific family of plant SGNH esterases involved in response to dehydration and cuticle formation. These results suggest that OsEST1 is not a lipase but an esterase activity which has some other function in rice, especially during seed development. 相似文献
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