4.5 Article

High-yield secretion of multiple client proteins in Aspergillus

期刊

ENZYME AND MICROBIAL TECHNOLOGY
卷 51, 期 2, 页码 100-106

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.enzmictec.2012.04.008

关键词

Protein production; Protein secretion; Fungi; Heterologous expression and secretion of multiple proteins

资金

  1. Department of Energy [06103-OKL, ZDJ-7-77608-01]
  2. Oklahoma Bioenergy Center award [06103-OKL]
  3. FAPESP (Brazil) [08/58037-9, 2008/58877-4, 2010/18198-3]
  4. CNPq (Brazil) [141133/2009-0]
  5. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [10/18198-3, 08/58037-9] Funding Source: FAPESP

向作者/读者索取更多资源

Production of pure and high-yield client proteins is an important technology that addresses the need for industrial applications of enzymes as well as scientific experiments in protein chemistry and crystallization. Fungi are utilized in industrial protein production because of their ability to secrete large quantities of proteins. In this study, we engineered a high-expression-secretion vector, pEXPYR that directs proteins towards the extracellular medium in two Aspergillii host strains, examine the effect of maltose-induced over-expression and protein secretion as well as time and pH-dependent protein stability in the medium. We describe five client proteins representing a core set of hemicellulose degrading enzymes that accumulated up to 50-100 mg/L of protein. Using a recyclable genetic marker that allows serial insertion of multiple genes, simultaneous hyper-secretion of three client proteins in a single host strain was accomplished. (c) 2012 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据