de Brito Ana Kezia Pimentel, Batista Samara Cláudia Picanço, Pimenta Laynah, Barbosa Elliza Emilly Perrone, Martim Salomão Rocha, Teixeira Maria Francisca Simas
Post-Graduate Program in Biotechnology, Federal University of Amazonas (UFAM), Manaus, Amazonas, 69067-005, Brazil.
DPUA Culture Collection, Universidade Federal Do Amazonas (UFAM), Manaus, Amazonas, 69067-005, Brazil.
Appl Biochem Biotechnol. 2025 Apr;197(4):2598-2609. doi: 10.1007/s12010-024-05155-3. Epub 2025 Jan 8.
Edible mushrooms have been used as sustainable sources of proteases of industrial interest. The aim of this research was to investigate the influence of different culture media on mycelial growth and the potential of an Amazonian mushroom species, Auricularia fuscosuccinea DPUA 1624, in the biosynthesis of bovine milk coagulant enzymes. The species was cultivated on Sabouraud agar, malt, glucose, and peptone agar, malt extract agar, and glucose and peptone agar, supplemented with yeast extract for mycelial development. Enzyme biosynthesis was evaluated by submerged fermentation. Subsequently, the cultures were incubated at 28 °C for 8 days. Proteolytic and coagulant activities were determined using 1% azocasein solution and milk powder as substrates, respectively. In the results of radial growth speed of A. fuscosuccinea, the values were significant in the GYP and SAB + YE culture media. However, GYP agar favored the growth and mycelial vigor of A. fuscosuccinea; therefore, this medium was selected to obtain inoculum in the tests. In submerged fermentation, the MGYP medium favored the synthesis of proteases for A. fuscosuccinea and synthesized coagulant proteases in 100% of the media, in which significant activity was observed in SAB + YE. The significant production of coagulant proteases of A. fuscosuccinea was obtained under the following conditions: inoculum size 10%, 8 days of fermentation period, and 8 days of inoculum age. The results indicate that A. fuscosuccinea DPUA 1624 has potential for use in industrial manufacturing, especially in dairy products.
可食用蘑菇一直被用作具有工业价值的蛋白酶的可持续来源。本研究的目的是调查不同培养基对菌丝生长的影响,以及亚马逊蘑菇物种——皱木耳 DPUA 1624 在牛凝乳酶生物合成中的潜力。该物种在添加酵母提取物以促进菌丝发育的沙氏琼脂、麦芽、葡萄糖和蛋白胨琼脂、麦芽提取物琼脂以及葡萄糖和蛋白胨琼脂上培养。通过深层发酵评估酶的生物合成。随后,将培养物在 28°C 下孵育 8 天。分别以 1% 偶氮酪蛋白溶液和奶粉为底物测定蛋白水解活性和凝乳活性。在皱木耳的径向生长速度结果中,GYP 和 SAB + YE 培养基中的值具有显著性。然而,GYP 琼脂有利于皱木耳的生长和菌丝活力;因此,选择该培养基在试验中获得接种物。在深层发酵中,MGYP 培养基有利于皱木耳蛋白酶的合成,并且在 100% 的培养基中合成了凝乳蛋白酶,其中在 SAB + YE 中观察到显著活性。在以下条件下获得了皱木耳凝乳蛋白酶的显著产量:接种量 10%、发酵期 8 天和接种龄 8 天。结果表明,皱木耳 DPUA 1624 具有用于工业生产的潜力,特别是在乳制品生产中。