首页> 外文期刊>Enzyme and Microbial Technology >Depolymerization of lignosulfonates by submerged cultures of the basidiomycete Irpex consors and cloning of a putative versatile peroxidase
【24h】

Depolymerization of lignosulfonates by submerged cultures of the basidiomycete Irpex consors and cloning of a putative versatile peroxidase

机译:拟南芥属Irpex cons浸没培养物对木质素磺酸盐的解聚作用,并克隆了一种假定的通用过氧化物酶

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Lignosulfonates are abundantly available byproducts of the paper and pulping industry, and they therefore represent a promising feedstock for new sustainable processes. For industrial applications of lignosulfonates, their molecular weight distribution is a critical factor. In order to decrease the average molecular weight of lignosulfonates, Seventeen basidiomycetes were screened for their capability to depolymerize lignosulfonates from spent sulfite liquor (SSL) in surface and liquid cultures. Five basidiomycetes polymerized the lignosulfonates under the selected conditions. Only Irpex consors was found to efficiently degrade calcium lignosulfonates when SSL (0.5%, w/w) was used as the sole carbon and nitrogen source. The average molecular weight of the lignosulfonates was reduced from similar to 26 to similar to 4 kDa as determined by size exclusion chromatography (SEC) within two weeks. Various extracellular enzyme activities of I. consors were determined over the culture period. High peroxidase activities were correlating with a high degradation rate and the culture was harvested at the day of highest peroxidase activity. A putative versatile peroxidase was isolated by fast protein liquid chromatography (FPLC) and its encoding cDNA was cloned. (C) 2015 Elsevier Inc. All rights reserved.
机译:木质素磺酸盐是造纸和制浆工业中大量可用的副产品,因此它们代表了新的可持续工艺的有前途的原料。对于木质素磺酸盐的工业应用,其分子量分布是关键因素。为了降低木质素磺酸盐的平均分子量,筛选了十七种担子菌在表面和液体培养物中从废亚硫酸盐溶液(SSL)解聚木质素磺酸盐的能力。在选定条件下,五种担子菌使木质素磺酸盐聚合。当SSL(0.5%,w / w)被用作唯一的碳和氮源时,只有Irpex补偿剂可有效降解木质素磺酸钙。如通过尺寸排阻色谱法(SEC)在两周内测定,木质素磺酸盐的平均分子量从相似的26降低至相似的4kDa。在培养期间确定了肠球菌的各种细胞外酶活性。高过氧化物酶活性与高降解速率相关,并且在过氧化物酶活性最高的当天收获培养物。通过快速蛋白质液相色谱法(FPLC)分离了一种推定的通用过氧化物酶,并克隆了其编码cDNA。 (C)2015 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号