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Purification and Characterization of Alkaline Pectin Lyase from a Newly Isolated Bacillus clausii and Its Application in Elicitation of Plant Disease Resistance

机译:新分离的克劳氏芽孢杆菌碱性果胶裂解酶的纯化,鉴定及其在植物抗病性诱导中的应用

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摘要

Alkaline pectin lyase (PNL) shows potential as a biological control agent against several plant diseases. We isolated and characterized a new Bacillus clausii strain that can produce 4,180 U/g of PNL using sugar beet pulp as a carbon source and inducer. The PNL was purified to apparent homogeneity using ultrafiltration, ammonium sulfate fractionation, DEAE Sepharose Fast Flow, and Sephadex G-75 gel filtration. The purified PNL was found to be a monomeric protein with a molecular weight of 35 kDa, as determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). It demonstrated optimal activity with K (m) of 0.87 mg/ml at pH 10.0 and 60 A degrees C. The enzyme is stable in the pH range of 8.0-10.0 and temperature a parts per thousand currency sign40 A degrees C. Ca2+ was found to stimulate the enzymatic activity of the PNL by up to 410 %. Mass spectrometric results gave 38 % match coverage with pectate lyase from B. clausii KSM-K16 (gi|56961845). The PNL was found to elicit disease resistance in cucumber seedlings, suggesting that it may have applications in biocontrol and sustainable agriculture.
机译:碱性果胶裂解酶(PNL)显示出作为针对几种植物病害的生物防治剂的潜力。我们分离并鉴定了一种新的克劳氏芽孢杆菌菌株,该菌株可以用甜菜粕作为碳源和诱导剂生产4,180 U / g PNL。使用超滤,硫酸铵分级分离,DEAE Sepharose Fast Flow和Sephadex G-75凝胶过滤将PNL纯化至表观均匀性。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)测定,发现纯化的PNL是分子量为35kDa的单体蛋白。它在pH 10.0和60 A的温度下具有0.87 mg / ml的K(m)表现出最佳活性。该酶在8.0-10.0的pH范围内稳定,温度为每千货币单位百万分之40A。发现Ca2 +刺激PNL的酶促活性高达410%。质谱分析结果显示,克劳氏芽孢杆菌KSM-K16(gi | 56961845)的果胶酸裂合酶具有38%的匹配覆盖率。发现PNL在黄瓜幼苗中引起抗病性,表明它可能在生物防治和可持续农业中具有应用。

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