不同碳氮源对环青霉果胶酶生物合成的影响

A. Kalieva, R. Blieva, G. Admanova, Bakshagul Bakytzhankyzy, Nazerke Kenzhalyevna Kemalova
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摘要

本文研究了碳源和氮源对环青霉果胶酶生物合成的影响。营养培养基中的碳氮源不仅影响环木的建设性代谢,而且影响果胶酶的合成。结果表明,果糖是最佳碳源,可使聚甲基半乳糖醛酸酶(PMGL)和聚半乳糖醛酸酶(PGL)在培养液中积累5.0和5.7单位/ml。最好的氮源是氯化铵。将其作为唯一氮源添加到营养培养基中,果胶酶的生物合成量与对照相比,聚甲基半乳糖醛酸酶(PMGL)提高了2.8倍,聚半乳糖醛酸酶(PGL)提高了3.0倍。菌丝产量提高到9.2 ~ 11.4单位/g。果胶酶生长和生物合成的最佳pH值为pH - 8.5。每24小时测定培养液中果胶酶活性和菌丝体生物量。整个生长过程持续了168小时。酶的生物合成在静止期最活跃,持续3.0-3.5天,培养4天后酶的活性急剧下降。结果表明,环孢霉果胶酶的生物合成具有组成性。特异性底物不诱导酶的生物合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of various carbon and nitrogen sources on the biosynthesis of pectinliase enzymes in Penicillium cyclopium
This article studies the effect of carbon and nitrogen sources on the biosynthesis of pectinliase enzymes in Penicillium cyclopium. The carbon and nitrogen sources in the nutrient medium influence not only the constructive metabolism of P. cyclopium but also the synthesis of pectinliase enzymes. It is found that the best carbon source is fructose, which provides accumulation of polymethylgalacturonatliase (PMGL) and polygalacturonatliase (PGL) in culture fluid up to 5.0 and 5.7 units/ml. The best nitrogen source is ammonium chloride. When it was added to the nutrient medium as the only nitrogen source, the biosynthesis of pectinliase enzymes increased 2.8 times for polymethylgalacturonatliase (PMGL) and 3.0 times for polygalacturonatliase (PGL) compared with the control. The productivity of the culture increased to 9.2–11.4 units/g of mycelium. The optimal pH value for the growth and pectinliase enzymes biosynthesis was pH — 8.5. Determination of the activity of pectinliase enzymes and mycelium biomass in the culture fluid was carried out every 24 hours. The duration of the entire growing process lasted 168 hours. The most active enzyme biosynthesis takes place in the stationary phase for 3.0–3.5 days, followed by a sharp drop in activity after 4 days of cultivation. It is identified that the biosynthesis of pectinliase enzymes in P. cyclopium has a constitutive nature. Specific substrates did not induce the enzymes biosynthesis.
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