Department of Biology, Faculty of Science, Shahid Bahonar University of Kerman, Kerman, Iran.
Soil and Water Research, Kerman Agricultural and Natural Resources Research and Education Center, AREEO, Kerman, Iran.
Arch Microbiol. 2021 Dec 28;204(1):88. doi: 10.1007/s00203-021-02713-9.
Cellulosic biomass is considered one of the most promising sources for the production of alternative renewable bioenergy and other valuable products. Identification and optimization of strains with high enzymatic activity that can overcome constraints imposed by the cellulosic structure is an essential step in the development of new biotechnologies. The aim of this study was to isolate and identify thermophilic (50 °C) and mesophilic (37 °C) cellulolytic bacteria from soil and leaves samples at Kerman, Iran. Degrader bacteria were isolated using serial dilution and pour plate method. Media contained carboxymethylcellulose (CMC), and filter paper was used as sources of carbon. Totally 22 mesophilic and 17 thermophilic bacterial strains which produced clear zones were further identified by morphological and biochemical tests. Screening of purified bacteria was performed to identify cellulase-producing bacteria by Congo red test. These bacteria were compared to each other based on cellulase activity, the percentage of growth, and extracellular protein amounts. The strains with the highest enzymatic activity were determined by the DNS method. The isolated US5 and US7 grew rapidly, and produced cellulase. The US5 created the largest clear zones (7 mm). Besides, these strains were selected for analysis of 16S rRNA sequence. The results showed that selected bacteria strains belong to Brevibacillus borstelensis. The B. borstelensis strains isolated in this study showed a suitable cellulase enzyme activity.
纤维素生物质被认为是生产替代可再生生物能源和其他有价值产品的最有前途的来源之一。鉴定和优化具有高酶活性的菌株,这些菌株能够克服纤维素结构带来的限制,是开发新技术的重要步骤。本研究的目的是从伊朗克尔曼的土壤和叶片样本中分离和鉴定嗜热(50°C)和嗜温(37°C)纤维素分解菌。采用连续稀释和倾注平板法分离降解菌。培养基中含有羧甲基纤维素(CMC),滤纸用作碳源。通过形态学和生化试验进一步鉴定产生清晰区的 22 株嗜温菌和 17 株嗜热菌。通过刚果红试验对纯化细菌进行筛选,以鉴定产纤维素酶的细菌。根据纤维素酶活性、生长百分比和胞外蛋白含量对这些细菌进行比较。用 DNS 法测定具有最高酶活性的菌株。分离的 US5 和 US7 生长迅速,并产生纤维素酶。US5 产生的透明圈最大(7mm)。此外,这些菌株被选择用于 16S rRNA 序列分析。结果表明,所选细菌菌株属于短芽孢杆菌。本研究中分离的 B. borstelensis 菌株表现出适宜的纤维素酶活性。