利用酒糟浸没式栽培黑木耳产生漆酶和生物量

Biomass Pub Date : 2023-12-19 DOI:10.3390/biomass4010001
Georgios Bakratsas, Kyriakos Antoniadis, Panagiotis E. Athanasiou, P. Katapodis, H. Stamatis
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引用次数: 0

摘要

葡萄酒业每年都会产生大量的酒糟。酒糟中含有大量酚类物质,如果不经过适当处理,就不适合丢弃到环境中或动物饲料中。在这项研究中,酒糟在浸没式栽培过程中经过浮游生物处理,产生了高价值的生物量和高水平的漆酶,漆酶是一种重要的工业酶。在初始 pH 值为 6.0、20% v/v 酒糟、30 克/升葡萄糖和 20 克/升酵母提取物的最佳条件下,生物量和漆酶产量分别达到 21 克/升和 74,000 单位/升,废物的脱色率和脱酚率超过 90%。菌丝生物量富含蛋白质和必需氨基酸,分别达到干重的 43% 和 16%。碳水化合物和脂类是生物质中第二丰富的生物活性化合物,含量分别为 29.4 ± 2.7% 和 29.5 ± 2.7%。通过简单的两步纯化程序,培养上清液中的粗漆酶被纯化了 4.4 倍,回收率为 44%。经 SDS 电泳测定,该酶的分子量为 62 kDa。在 pH 值为 5.0 和温度为 70 ℃ 时,酶的活性最佳。酶的活化能计算值为 20.0 ± 0.2 kJ/mol。研究了纯化漆酶的 pH 稳定性和热稳定性。该酶在 pH 值为 8.0 和高达 40 °C 的温度下非常稳定。经测定,该酶的热失活能量为 76.0 ± 1.2 kJ/mol。在 20-60 °C 的温度范围内,纯化漆酶热失活的热力学参数(ΔH*、ΔG* 和 ΔS*)为73.8 ≤ ΔH* ≤ 74.3 kJ-mol-1,98.7 ≤ ΔG* ≤ 101.9 kJ-mol-1,-90.5 ≤ ΔS* ≤ -84.3 J-mol-1-K-1。酒糟可作为培养真菌的理想基质,以更环保的方式生产漆酶和高蛋白生物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Laccase and Biomass Production via Submerged Cultivation of Pleurotus ostreatus Using Wine Lees
Large quantities of wine lees are produced annually by the wine industry. The high phenolic content makes them unsuitable for disposal in the environment or animal feed without a suitable treatment. In this study, wine lees were treated by Pleurotus ostreatus in submerged cultivation, producing a high-value biomass and elevated levels of laccase, an important industrial enzyme. Biomass and laccase production reached 21 g/L and 74,000 Units/L, respectively, at the optimal conditions of initial pH 6.0, 20% v/v wine lees, 30 g/L glucose, and 20 g/L yeast extract, while decolorization and dephenolization rates of the waste were over 90%. The mycelial biomass was rich in proteins and essential amino acids reaching up to 43% and 16% per dry weight, respectively. Carbohydrates and lipids were the second richest bioactive compound in biomass, with values of 29.4 ± 2.7% and 29.5 ± 2.7%, respectively. The crude laccase in the culture supernatant was purified via a simple two-step purification procedure by 4.4-fold with a recovery of 44%. The molecular weight of the enzyme was determined to be 62 kDa via SDS electrophoresis. Enzyme activity was optimal at pH 5.0 and 70 °C. The activation energy of the enzyme was calculated at a value of 20.0 ± 0.2 kJ/mol. The pH stability and thermostability of the purified laccase were studied. The enzyme was remarkably stable at pH 8.0 and at temperatures up to 40 °C. The thermal inactivation energy of the enzyme was determined to be 76.0 ± 1.2 kJ/mol. The thermodynamic parameters (ΔH*, ΔG*, and ΔS*) for the thermal deactivation of the purified laccase at a temperature range of 20–60 °C were: 73.8 ≤ ΔH* ≤ 74.3 kJ·mol−1, 98.7 ≤ ΔG* ≤ 101.9 kJ·mol−1, and −90.5 ≤ ΔS* ≤ −84.3 J·mol−1·K−1. Wine lees could be ideal substrates of fungal cultivation for laccase production and biomass with a high protein content in an eco-friendlier way.
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