Pengaruh Variasi Media Pertumbuhan terhadap Aktivitas Peredaman Radikal Bebas DPPH Ekstrak Kapang Endofit Isolat Cb.D1

Ayu Purnamasari, Fitri Andriyaningsih, Riska Andriani Pamungkas, Eris Septiana
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Abstract

Endophytic fungi are a source of antioxidant compounds in nature. The low yield of extracts and active compounds produced is one of the limiting factors for using endophytic fungi as a source of natural antioxidant compounds. Modification of growth media is an alternative solution to overcome this problem. This study aimed to determine the effect of media conditions, belonging to carbon and nitrogen sources and different initial pH of fermentation, on the antioxidant through DPPH radical scavenging activity of extract of endophytic fungi Cb.D1 isolated from cinnamon plant leaves. The culture was propagated using Czapek Dox Broth basal liquid medium with agitation speed 120 rpm at room temperature for 14 days. The carbon sources used were glucose, sucrose, and soluble starch. The nitrogen sources were natrium nitrate, ammonium nitrate, and yeast extract. The initial pH conditions used were 5, 7, and 9, and ethyl acetate as the extraction solvent. The results obtained that the variation of nitrogen and carbon sources and also initial pH conditions can increase the yield of extract of endophytic fungi Cb.D1. Glucose, yeast extract, and initial pH at 9 were the best growth media to gain it. The substitution of nitrogen sources and initial pH can increase the DPPH free radical scavenging activity of endophytic fungal extract compared to substitution for carbon sources. The highest activity from the Cb.D1 endophytic fungal extract was obtained from media that contain sucrose and natrium nitrate as a carbon and nitrogen sources and an initial pH of 5. The Variation of growth media of endophytic fungi Cb.D1 affected their extract in DPPH free radical scavenging activity.
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介质变异编辑器生长对抗Cb.D1分离的Endofit提取物DPPH自由基缺失活性
内生真菌是自然界中抗氧化化合物的来源。所产生的提取物和活性化合物的低产量是使用内生真菌作为天然抗氧化化合物来源的限制因素之一。改良生长介质是克服这一问题的另一种解决方案。本研究旨在通过从肉桂植物叶片中分离的内生真菌Cb.D1提取物的DPPH自由基清除活性,确定属于碳源和氮源以及不同发酵初始pH的培养基条件对抗氧化剂的影响。使用Czapek Dox Broth基础液体培养基在室温下以120rpm的搅拌速度繁殖培养物14天。使用的碳源是葡萄糖、蔗糖和可溶性淀粉。氮源为硝酸钠、硝酸铵和酵母提取物。使用的初始pH条件为5、7和9,乙酸乙酯作为提取溶剂。结果表明,氮源和碳源以及初始pH条件的变化可以提高内生真菌Cb.D1的提取物产量。葡萄糖、酵母提取物和初始pH值为9是获得DPPH的最佳生长培养基。与碳源替代相比,氮源和初始pH的替代可以提高内生真菌提取物对DPPH自由基的清除活性。Cb.D1内生真菌提取物的最高活性是从含有蔗糖和硝酸钠作为碳源和氮源并且初始pH为5的培养基中获得的。内生真菌Cb.D1生长培养基的变化影响其提取物对DPPH自由基的清除活性。
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审稿时长
16 weeks
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