Institute of Microbiology, Chair of Molecular Biotechnology, Technische Universität Dresden, 01062, Dresden, Germany,
Appl Microbiol Biotechnol. 2014 Feb;98(4):1517-29. doi: 10.1007/s00253-013-5441-5. Epub 2013 Dec 21.
Cofactor-dependent enzymes catalyze a broad range of synthetically useful transformations. However, the cofactor requirement also poses economic and practical challenges for the application of these biocatalysts. For three decades, considerable research effort has been devoted to the development of reliable in situ regeneration methods for the most commonly employed cofactors, particularly NADH and NADPH. Today, researchers can choose from a plethora of options, and oxidoreductases are routinely employed even on industrial scale. Nevertheless, more efficient cofactor regeneration methods are still being developed, with the aim of achieving better atom economy, simpler reaction setups, and higher productivities. Besides, cofactor dependence has been recognized as an opportunity to confer novel reactivity upon enzymes by engineering their cofactors, and to couple (redox) biotransformations in multi-enzyme cascade systems. These novel concepts will help to further establish cofactor-dependent biotransformations as an attractive option for the synthesis of biologically active compounds, chiral building blocks, and bio-based platform molecules.
辅因子依赖的酶可以催化广泛的具有合成应用价值的转化。然而,辅因子的要求也给这些生物催化剂的应用带来了经济和实际的挑战。三十年来,人们投入了大量的研究精力来开发最常用的辅因子(特别是 NADH 和 NADPH)的可靠原位再生方法。如今,研究人员可以有多种选择,并且氧化还原酶甚至在工业规模上也得到了常规应用。然而,人们仍在开发更有效的辅因子再生方法,旨在实现更好的原子经济性、更简单的反应装置和更高的生产率。此外,人们已经认识到辅因子依赖性是通过工程化酶的辅因子赋予酶新反应性的机会,并在多酶级联系统中偶联(氧化还原)生物转化。这些新的概念将有助于进一步将辅因子依赖的生物转化确立为合成生物活性化合物、手性砌块和生物基平台分子的有吸引力的选择。