Larsen Øivind, Bjerga Gro Elin Kjæreng
Centre for Applied Biotechnology, Uni Research AS, Thormøhlens gt. 55, N-5006 Bergen, Norway.
Microorganisms. 2018 Jun 7;6(2):51. doi: 10.3390/microorganisms6020051.
The discovery of new enzymes for industrial application relies on a robust discovery pipeline. Such a pipeline should facilitate efficient molecular cloning, recombinant expression and functional screening procedures. Previously, we have developed a vector set for heterologous expression in . Here, we supplement the catalogue with vectors for expression in The vectors are made compatible with a versatile cloning procedure based on type IIS restriction enzymes and T4 DNA ligase, and encompass an effective counter-selection procedure and complement the set of vectors with options for secreted expression. We validate the system with expression of recombinant subtilisins, which are generally challenging to express in a heterologous system. The complementarity of the and systems allows rapid switching between the two commonly used hosts without comprehensive intermediate cloning steps. The vectors described are not limited to the expression of certain enzymes, but could also be applied for the expression of other enzymes for more generalized enzyme discovery or development.
用于工业应用的新酶的发现依赖于一个强大的发现流程。这样的流程应便于高效的分子克隆、重组表达和功能筛选程序。此前,我们已开发了一套用于在……中进行异源表达的载体。在此,我们补充了用于在……中表达的载体目录。这些载体与基于IIS型限制酶和T4 DNA连接酶的通用克隆程序兼容,包含有效的反选择程序,并补充了分泌表达选项的载体集。我们用重组枯草杆菌蛋白酶的表达来验证该系统,重组枯草杆菌蛋白酶在异源系统中通常难以表达。……和……系统的互补性允许在两个常用宿主之间快速切换,而无需全面的中间克隆步骤。所描述的载体不仅限于某些酶的表达,还可用于表达其他酶,以进行更广泛的酶发现或开发。