地衣芽孢杆菌MY75菌株几丁质酶基因的异源表达及特性

【目的】地衣芽孢杆菌MY75菌株的几丁质酶基因的异源表达,并对表达蛋白的特性进行研究。【方法】制备MY75菌株培养上清粗蛋白,利用酶谱分析确定具有几丁质酶活的蛋白分子量。将该蛋白进行飞行时间质谱分析,确定其部分氨基酸序列,设计PCR引物对MY75菌株的几丁质酶基因进行克隆及异源表达。对表达蛋白的最适反应温度及pH,温度耐受性及金属离子对酶活力的影响等特性进行了研究,并测定了表达蛋白对真菌孢子萌发的抑制活性和对甜菜夜蛾幼虫的杀虫增效作用。【结果】酶谱分析证明MY75菌株培养上清液中仅含有一种55kDa的几丁质酶。将该编码基因chiMY克隆及序列分析后发现,基因长度为1797bp,编码599个氨基酸。在大肠杆菌中异源表达的几丁质酶ChiMY蛋白的分子量为67kDa。质谱分析证明,55kDa蛋白与67kDa蛋白序列相同。ChiMY最适pH和最适温度分别为7.0和50°C,为中性几丁质酶。Li+,Na+,和Mg2+离子对表达蛋白的酶活力具有促进作用,Mn2+,Cr3+,Zn2+和Ag+离子则能显著抑制酶活力,Cu2+和Fe3+离子完全抑制酶活性。生物测定的结果显示,异源表达的MY75几丁质酶能够抑制小麦赤霉及黑曲霉的孢子萌发,并且对苏云金芽孢杆菌的杀虫活力具有增效作用。【结论】地衣芽孢杆菌MY75菌株中仅有一种55kDa几丁质酶,其编码基因能够在大肠杆菌中大量表达,表达蛋白分子量与野生型蛋白之间有显著差异,由此证明MY75菌株中存在着几丁质酶的剪切加工过程。明确了地衣芽孢杆菌几丁质酶ChiMY具有抑制真菌活性及杀虫增效作用。上述全部研究结论在国内首次报道。

Heterogeneous expression of chitinase gene from Bacillus licheniformis MY75 and the characterization of expressed ChiMY

Abstract: Objective] To heterogeneously express the chitinase gene of Bacillus licheniformis strain MY75 in E. coli, and to characterize the recombinant chitinase ChiMY. Methods] The extracelluar crude protein from B. licheniformis MY75 was analyzed by zymogram analysis. The partial amino acid sequence of the protein owned chitinase activity was given by time-of-flight mass spectrometry (TOF-MS). Then the corresponding chitinase gene chiMY was cloned and heterogeneously expressed in E. coli. The optimum temperature and pH of the ChiMY, and the effect of various metal ions on chitinase activity were studied. The antifungal activity and the synergistic effect on insecticidal activity were demonstrated by bioassays. Results] A 55 kDa extracelluar protein produced by B. licheniformis MY75 exhibited chitinase activity in zymogram analysis. The chiMY gene was 1797 bp long and encoded a 599 amino acid protein. The molecular weight of the recombinant protein ChiMY over-expressed in E. coli was 67 kDa. The amino acid sequence of the 55 kDa extracelluar protein was proved identical to the 67 kDa ChiMY by the TOF-MS. The optimum temperature and pH were 50 °C and 7.0, respectively. The enzyme activity was improved by Li+, Na+ and Mg2+ and inhibited by Mn2+, Cr3+, Zn2+, and Ag+. Cu2+ and Fe3+ can inactivate the enzyme. The bioassays demonstrated the heterogeneous expressed ChiMY could inhibit the sporangia germination of G. saubinetii and A. niger. and reduce the LC50 (50 % lethal concentration) of the crystal protein of Bacillus thuringiensis against S. exigua by approximately 27 %. Conclusions] The B. licheniformis MY75 could produce a 55 kDa chitinase. The corresponding chitinase gene was over-expressed in E. coli. The molecular weight of heterogeneous expressed ChiMY showed significant different to the wild-type chitinase protein. This implicated the the protein processing of chitinase in the B. licheniformis MY75. The ChiMY also owned the antifungal activity and could improve the insecticidal activity of the Bacillus thuringiensis crystal protein against to S. exigua. This is the first report about the chitinase from B. licheniformis in China.