We have developed an efficient optimization technique, 'biased mutation-assembling', for improving protein properties such as thermostability. In this strategy, a mutant library is constructed using the overlap extension polymerase chain reaction technique with DNA fragments from wild-type and phenotypically advantageous mutant genes, in which the number of mutations assembled in the wild-type gene is stochastically controlled by the mixing ratio of the mutant DNA fragments to wild-type fragments. A high mixing ratio results in a mutant composition biased to favor multiple-point mutants. We applied this strategy to improve the thermostability of prolyl endopeptidase from Flavobacterium meningosepticum as a case study and found that the proportion of thermostable mutants in a library increased as the mixing ratio was increased. If the proportion of thermostable mutants increases, the screening effort needed to find them should be reduced. Indeed, we isolated a mutant with a 1200-fold longer activity half-life at 60°C than that of wild-type prolyl endopeptidase after screening only 2000 mutants from a library prepared with a high mixing ratio. Our results indicate that an aggressive accumulation of advantageous mutations leads to an increase in the quality of the mutant library and a reduction in the screening effort required to find superior mutants. © The Author 2005. Published by Oxford University Press. All rights reserved.
CITATION STYLE
Hamamatsu, N., Aita, T., Nomiya, Y., Uchiyama, H., Nakajima, M., Husimi, Y., & Shibanaka, Y. (2005). Biased mutation-assembling: An efficient method for rapid directed evolution through simultaneous mutation accumulation. Protein Engineering, Design and Selection, 18(6), 265–271. https://doi.org/10.1093/protein/gzi028
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