Sen S, Venkata Dasu V, Mandal B
Centre for the Environment, Indian Institute of Technology-Guwahati, Guwahati, Assam, 781039, India.
Appl Biochem Biotechnol. 2007 Dec;143(3):212-23. doi: 10.1007/s12010-007-8003-4.
The engineering of enzymes with altered activity, specificity, and stability, using directed evolution techniques that mimic evolution on a laboratory timescale, is now well established. In vitro recombination techniques such as DNA shuffling, staggered extension process (StEP), random chimeragenesis on transient templates (RACHITT), iterative truncation for the creation of hybrid enzymes (ITCHY), recombined extension on truncated templates (RETT), and so on have been developed to mimic and accelerate nature's recombination strategy. This review discusses gradual advances in the techniques and strategies used for the directed evolution of biocatalytic enzymes aimed at improving the quality and potential of enzyme libraries, their advantages, and disadvantages.
利用在实验室时间尺度上模拟进化的定向进化技术来改造酶的活性、特异性和稳定性,如今已得到充分确立。诸如DNA改组、交错延伸过程(StEP)、基于瞬时模板的随机嵌合诱变(RACHITT)、用于创建杂交酶的迭代截短(ITCHY)、基于截短模板的重组延伸(RETT)等体外重组技术已被开发出来,以模拟和加速自然界的重组策略。本综述讨论了用于生物催化酶定向进化的技术和策略的逐步进展,旨在提高酶文库的质量和潜力,以及它们的优缺点。