Rebhika Lusiana, Achmad Toto Poernomo, Achmad Syahrani
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引用次数: 0
摘要
在全世界,心血管疾病(cvd)是导致死亡的主要原因。对于心血管疾病的治疗,微生物纤溶酶被高度认为是一种新的治疗候选者。本研究旨在测定真菌源小孢子根霉(Rhizopus microsporus var. oligosporus) FNCC 6010对向日葵(Helianthus annuus)种子和菜豆(Phaseolus vulgaris)种子发酵后产生的纤溶蛋白酶活性。采用固态发酵法发酵,初始pH为5,培养温度为33±1℃,培养时间为24小时。提取发酵后的种子得到上清液作为粗酶。蛋白水解活性测定采用脱脂乳琼脂(SMA)平板法获得蛋白水解指数,纤溶活性测定采用纤维蛋白-琼脂糖平板法获得纤溶指数。结果表明,小孢子镰刀菌发酵的黄芪和黄芪种子粗酶具有纤溶酶活性,蛋白酶水解指数分别为2.64±0.01和2.23±0.04。纤溶指数分别为2.40±0.06和1.64±0.06。因此,粗酶作为一种候选溶栓剂具有进一步研究的潜力。酶的纯化、表征和深入研究是开发预防和治疗心血管疾病制剂的必要条件。
Fibrinolytic Protease Activity of Crude Enzyme from Fermented Sunflower (Helianthus annuus) and Common Bean (Phaseolus vulgaris) seeds by Rhizopus microsporus var. oligosporus FNCC 6010 in Solid State Fermentation
In the entire world, cardiovascular diseases (CVDs) are the main cause of death. For the treatment of CVDs, microbial fibrinolytic enzymes are highly regarded as novel therapeutic candidates. This study was purposed to determine the fibrinolytic protease activity produced by fungus source, which is Rhizopus microsporus var. oligosporus FNCC 6010 in fermented sunflower (Helianthus annuus) seed and common bean (Phaseolus vulgaris) seed. Fermentation was carried out by solid-state fermentation method at an initial pH of 5, incubation temperature of 33±1°C, and incubation time of 24 hours. The fermented seed was extracted to obtain supernatant as the crude enzyme. The proteolytic activity assay was done by the skimmed milk agar (SMA) plate method to obtain the proteolytic index, and the fibrinolytic activity assay was conducted by the fibrin-agarose plate method to get the fibrinolytic index. The results show that crude enzymes from fermented H. annuus and P. vulgaris seeds by R. microsporus have fibrinolytic protease activity with proteolytic index 2.64 ± 0.01 and 2.23 ± 0.04, respectively. The fibrinolytic index is 2.40 ± 0.06 and 1.64 ± 0.06, respectively. Therefore, the crude enzyme has the potential to be further researched as a candidate for thrombolytic agents. The purification, characterization, and in-depth research are needed to develop enzymes into preparations for preventing and treating CVDs.