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首页> 外文期刊>Revista Brasileira de Parasitologia Veterinária >Proteolytic action of the crude extract ofDuddingtonia flagrans on cyathostomins (Nematoda: Cyathostominae) in coprocultures
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Proteolytic action of the crude extract ofDuddingtonia flagrans on cyathostomins (Nematoda: Cyathostominae) in coprocultures

机译:鞭毛鞭毛藻粗提物对共培养中的寄宿生蛋白(线虫:Cyathostominae)的蛋白水解作用。

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摘要

The objective of this study was to examine the action of the crude extract of Duddingtonia flagrans (isolates AC001 and CG722) on infective larvae (L3) of cyathostomins in coprocultures and to confirm its proteolytic activity by means of a zymogram. The following groups were formed in coprocultures: Group 1: 10 mL of crude extract of D. flagrans (AC001); group 2: 10 mL of crude extract of AC001 with 10 mM of Ca2+; group 3: 10 mL of crude extract of D. flagrans (CG722); group 4: 10 mL of crude extract of CG722 with 10 mM of Ca2+; and group 5: control group (distilled water). The third-stage larvae (L3) were obtained after eight days. The crude extract of D. flagrans was effective in reducing the number of L3, with the following percentage reductions: group 1, 49.5%; group 2, 52.5%; group 3, 36.8%; and group 4, 57.7%; in relation to the control group (p 0.05). The proteolytic activity of the crude extract was confirmed through the zymogram. The results from this study confirmed that the crude extract of the fungusD. flagrans could be used for controlling cyathostomin L3, and suggested that at least one protease of approximately 38 kDa was present.
机译:这项研究的目的是检查鞭毛杜德通氏菌的粗提物(分离物AC001和CG722)对共培养中含寄主蛋白的感染性幼虫(L3)的作用,并通过酶谱确认其蛋白水解活性。在共培养物中形成以下几组:第1组:10 mL鞭毛粗提物(AC001);第2组:10 mL AC001粗提取物和10 mM Ca2 +;第3组:10 mL鞭毛粗提物(CG722)的粗提物;第4组:10 mL CG722粗提液和10 mM Ca2 +;第5组:对照组(蒸馏水)。八天后获得第三阶段的幼虫(L3)。 D.鞭毛的粗提物可有效减少L3的数量,减少百分比如下:第1组,49.5%;第二组,52.5%;第三组,36.8%;第4组,占57.7%;相对于对照组(p> 0.05)。通过酶谱图证实了粗提取物的蛋白水解活性。这项研究的结果证实了真菌D的粗提物。鞭毛可用于控制cyathostomin L3,并提示存在至少一种约38 kDa的蛋白酶。

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