Liu Wen-ping, Zeng Hong-mei, Liu Yan-feng, Yuan Jing-jing, Qiu De-wen
College of Plant Protection, Southwest University, Chongqing 400716, China.
Wei Sheng Wu Xue Bao. 2007 Aug;47(4):593-7.
A positive clone was screened from Alternaria tenuissima expression library. The result of sequencing and gene analysis indicated that the cloned DNA fragment has a complete ORF, which was named peaT2 (Protein Elicitor from Alternaria tenuissima 2) with the GenBank accession number EF212880. The gene was amplified by PCR and subcloned into the pPIC9K of Pichia pastoris expression system. The resulting recombinant plasmid pPIC9K/peaT2 was verified by sequencing and digested by Sac I. The linearized DNA was transformed into P. pastoris GS115 by electroporation. By means of MD and G418-YPD plates and PCR, the recombinant P. pastoris strains (his- mut+) were obtained. A recombinant clone cultivated on YPD plate with high concentration of G418 was randomly selected as expression strain. The protein expression was induced by methanol and analyzed by 12% SDS-PAGE. The results of SDS-PAGE and Western blot indicated that this gene was expressed successfully in P. pastoris with the induction of methanol. In BMMY culture medium, the expressed protein reached its maximum amount at 72h, whereas no corresponding protein was detected in the negative control. Bioassay was performed with the expressed protein. After soaking with the expressed protein for 8h, wheat seeds were cultured, the height of seedlings was measured after 24h, 36h, 48h, 7d, respectively, and the root length was measured after 7 days. The results showed that the expressed protein can promote seeding growth and root length obviously in appropriate concentration. It is revealed that PeaT2 can act as protein elicitor.
从细极链格孢菌表达文库中筛选出一个阳性克隆。测序和基因分析结果表明,克隆的DNA片段具有完整的开放阅读框,将其命名为peaT2(细极链格孢菌蛋白激发子2),GenBank登录号为EF212880。通过PCR扩增该基因,并亚克隆到毕赤酵母表达系统的pPIC9K中。对得到的重组质粒pPIC9K/peaT2进行测序验证,并用Sac I酶切。将线性化的DNA通过电穿孔法转化到毕赤酵母GS115中。通过MD和G418 - YPD平板以及PCR,获得了重组毕赤酵母菌株(his - mut +)。随机选择一株在高浓度G418的YPD平板上培养的重组克隆作为表达菌株。用甲醇诱导蛋白表达,并通过12% SDS - PAGE进行分析。SDS - PAGE和Western blot结果表明,该基因在甲醇诱导下在毕赤酵母中成功表达。在BMMY培养基中,表达的蛋白在72小时达到最大量,而阴性对照中未检测到相应蛋白。对表达的蛋白进行生物测定。用表达的蛋白浸泡小麦种子8小时后进行培养,分别在24小时、36小时、48小时、7天后测量幼苗高度,7天后测量根长。结果表明,表达的蛋白在适当浓度下能明显促进种子生长和根长。结果表明,PeaT2可作为蛋白激发子。