Mushroom residue extract-based media enhanced the enrichment and isolation of cellulose-degrading bacteria

Q1 Environmental Science
Xiaoli Luo , Tianshu Wang , Yili Meng , Li Li , Shuihong Yao , Huawei Wu , Jun Li
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Abstract

This study aims to develop substrate-specific media for targeted enrichment of cellulose-degrading bacteria from mushroom residue to increase composting efficiency. Mushroom residue extract-based media—MR (basic extract) and MRC (with sodium carboxymethyl cellulose)—were designed and comparatively analyzed against conventional LB medium. Both MR and MRC significantly increased bacterial alpha diversity and enriched key cellulose-degrading genera (e.g., Paenibacillus and Bacillus). Functional shifts were observed through the altered abundance of carbon-degrading genes (abfA, cex, lig) and nitrogen/phosphorus metabolism genes (nifH, gcd), indicating metabolic adaptation to lignocellulose-rich substrates. Critically, 35 cellulose-degrading strains with superior enzymatic activities were isolated (endoglucanase: 32.77–144.88 μg min−1; β-glucosidase: 49.99–122.34 μg min−1; filter paper activity: 38.82–169.34 μg min−1). Compared with LB-derived isolates, strains from MR/MRC media presented a 1.8–2.3-fold greater cellulose-degrading capacity. These findings demonstrate that substrate-specific media preferentially enrich functional consortia, providing tailored inoculants to accelerate composting and valorize agricultural waste.

Abstract Image

以香菇渣提取物为基础的培养基增强了纤维素降解菌的富集和分离
本研究旨在开发针对蘑菇渣中纤维素降解菌的培养基,以提高堆肥效率。设计了以香菇渣提取物为基础的mr(碱性提取物)和MRC(含羧甲基纤维素钠)培养基,并与常规LB培养基进行了对比分析。MR和MRC都显著增加了细菌α多样性,并丰富了关键的纤维素降解属(如芽孢杆菌和芽孢杆菌)。通过碳降解基因(abfA, cex, light)和氮/磷代谢基因(nifH, gcd)丰度的改变,观察到功能变化,表明对富含木质纤维素的底物的代谢适应。关键是,分离到35株纤维素降解菌,酶活性较高(内切葡聚糖酶:32.77 ~ 144.88 μg min−1;β-葡萄糖苷酶:49.99 ~ 122.34 μg min−1;滤纸活度:38.82 ~ 169.34 μg min−1)。与lb衍生的分离株相比,MR/MRC培养基中的菌株纤维素降解能力提高1.8 - 2.3倍。这些发现表明,特定基质培养基优先丰富功能联合体,提供量身定制的接种剂,以加速堆肥和农业废弃物的增值。
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来源期刊
Bioresource Technology Reports
Bioresource Technology Reports Environmental Science-Environmental Engineering
CiteScore
7.20
自引率
0.00%
发文量
390
审稿时长
28 days
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