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Improvement of Chitinase Production by Bacillus thuringiensis NM101-19 for Antifungal Biocontrol through Physical Mutation

机译:通过物理突变,通过物理突变提高胰蛋白酶胰蛋白盐杆菌的胰蛋白酶生成的胰蛋白酶生成

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摘要

Chitinase is one of the most important enzymes due to its diversity and a variety of potential uses. This study is an attempt to enhance chitinase production for antifungal biocontrol by subjecting Bacillus thuringiensis NM101-19 strain grown on shrimp shell wastes to various doses of gamma irradiation. Six mutants (BM-4, BM-6, BM-8, BM-12, BM-15, and BM-17) obtained at gamma ray doses of 40, 60, 80, 100, 120 and 140 Gy, respectively produced higher levels of chitinolytic activities in comparision to the wild-type strain. The BM-15 mutant strain showed the highest chitinase production (65.41 U/mL) which was 2.60 times more than the wild type (25.11 U/mL). Biocontrol efficacy of the mutants was statistically superior to the wild-type strain against all tested phytopathogens. Random amplified polymorphic DNA (RAPD) and inter simple sequence repeat (ISSR) PCR techniques, with five primers for each, were used in order to detect the variation in DNA profile between the mutant and wild-type strains in response to gamma-radiation treatments. RAPD and ISSR analysis indicated the appearance and disappearance of DNA polymorphic bands at different gamma ray doses. The results confirmed that the mutagenesis technique is a potent strategy to enhance the chitinase activity for industrial and agricultural purposes.
机译:Chitinase是由于其多样性和各种潜在用途导致的最重要的酶之一。该研究是通过在虾壳废弃物上生长的枯枝芽孢杆菌芽孢杆菌,增强对抗真菌生物控制的几丁质酶生产。在40,60,80,100,120和140Gy的γ射线剂量下获得六个突变体(BM-4,BM-6,BM-8,BM-12,BM-12,BM-17),分别产生更高野生型菌株比较的几丁质活性水平。 BM-15突变菌株显示出最高的几丁质酶生产(65.41u / ml),比野生型(25.11u / ml)多2.60倍。突变体的生物控制效果与所有测试的植物病变统计学上优于野生型菌株。随机扩增的多晶型DNA(RAPD)和单一简单的序列重复(ISSR)PCR技术,每种引物有五种引物,以检测突变体和野生型菌株之间的DNA曲线变异,响应于γ-辐射处理。 RAPD和ISSR分析表明DNA多晶段在不同γ射线剂量下的外观和消失。结果证实,诱变技术是增强工业和农业目的的几丁质酶活性的有效策略。

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