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优化嗜地真菌菌株对羽毛废料的生物降解条件,以进一步应用于农业。

Optimization of Conditions for Feather Waste Biodegradation by Geophilic Fungal Strains towards Further Agricultural Use.

机构信息

Department of Environmental Microbiology, Faculty of Agrobioengineering, University of Life Sciences in Lublin, Leszczyńskiego 7 Street, 20-069 Lublin, Poland.

出版信息

Int J Environ Res Public Health. 2022 Aug 31;19(17):10858. doi: 10.3390/ijerph191710858.

Abstract

The aim of the study was to optimize culture conditions and medium composition to accelerate the biodegradation of chicken feather waste by keratinolytic soil strains of , which are poorly known in this respect, as well as to propose hitherto unconsidered culture conditions for these fungi in order to obtain a biopreparation with a high fertilization value. Different pH of the medium, incubation temperatures, amounts of chicken feathers, additional carbon sources, and culture methods were tested. The process of optimizing keratin biodegradation was evaluated in terms of measuring the activity of keratinase, protease, disulfide reductase, concentration of released soluble proteins and peptides, total pool of amino acids, ammonium and sulfate ions, changes in medium pH, and feather weight loss. It was found that the studied fungal strains were capable of decomposing and mineralizing keratin from feather waste. Regarding the fertilizer value of the obtained hydrolysates, it was shown that the release of sulfate and ammonium ions was highest in a stationary culture containing 2% feathers with an initial pH of 4.5 and a temperature of 28 °C. Days 14-21 of the culture were indicated as the optimal culture time for these fungi to obtain biopreparations of high fertilizing value.

摘要

本研究旨在优化培养条件和培养基组成,以加速角蛋白水解土壤菌株对鸡毛废物的生物降解,而这些菌株在这方面的了解甚少,同时为这些真菌提出迄今尚未考虑的培养条件,以获得具有高施肥价值的生物制剂。测试了不同的培养基 pH 值、培养温度、鸡毛用量、额外的碳源和培养方法。根据测定角蛋白酶、蛋白酶、二硫键还原酶的活性、释放的可溶性蛋白质和肽的浓度、总氨基酸池、铵离子和硫酸根离子的浓度、培养基 pH 值的变化以及鸡毛失重,来评估角蛋白生物降解的优化过程。研究发现,所研究的真菌菌株能够分解和矿化鸡毛中的角蛋白。关于获得的水解物的肥料价值,结果表明,在含有 2%鸡毛、初始 pH 值为 4.5 和温度为 28°C 的静置培养物中,释放的硫酸根和铵离子最高。对于这些真菌来说,获得高施肥价值的生物制剂的最佳培养时间为 14-21 天。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f005/9518355/1c1060cf672d/ijerph-19-10858-g001.jpg

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