enzyme evolution
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Author(s):  
Gaspar P. Pinto ◽  
Marina Corbella ◽  
Andrey O. Demkiv ◽  
Shina Caroline Lynn Kamerlin

2021 ◽  
Vol 6 (2) ◽  
Author(s):  
Anthony Futerman

The biochemist Dan Tawfik passed away in May 2021 at age sixty-five and yet the height of his powers. Dan’s scientific research focused on proteins and, in particular, on enzyme evolution. Recently he had begun working on the most difficult challenge in biochemical evolution: reconstructing the metabolic pathways that may have led to the emergence of the first functional proteins.


Author(s):  
Jia Zheng ◽  
Sinisa Bratulic ◽  
Heidi E. L. Lischer ◽  
Andreas Wagner

2021 ◽  
Vol 69 ◽  
pp. 182-190
Author(s):  
Jovana Nazor ◽  
Joyce Liu ◽  
Gjalt Huisman
Keyword(s):  

JACS Au ◽  
2021 ◽  
Vol 1 (4) ◽  
pp. 508-516
Author(s):  
Emily E. Kempa ◽  
James L. Galman ◽  
Fabio Parmeggiani ◽  
James R. Marshall ◽  
Julien Malassis ◽  
...  

2021 ◽  
Author(s):  
Tian Yang ◽  
Zhixia Ye ◽  
Michael D Lynch

Enzyme evolution has enabled numerous advances in biotechnology. However, directed evolution programs can still require many iterative rounds of screening to identify optimal mutant sequences. This is due to the sparsity of the fitness landscape, which in turn, is due to hidden mutations that only offer improvements synergistically in combination with other mutations. These hidden mutations are only identified by evaluating mutant combinations, necessitating large combinatorial libraries or iterative rounds of screening. Here, we report a multi-agent directed evolution approach that incorporates diverse substrate analogues in the screening process. With multiple substrates acting like multiple agents navigating the fitness landscape, we are able to identify hidden mutant residues that impact substrate specificity without a need for testing numerous combinations. We initially validate this approach in engineering a malonyl-CoA synthetase for improved activity with a wide variety of non-natural substrates. We found that hidden mutations are often distant from the active site, making them hard to predict using popular structure-based methods. Interestingly, many of the hidden mutations identified in this case are expected to destabilize interactions between elements of tertiary structure, potentially affecting protein flexibility. This approach may be widely applicable to accelerate enzyme engineering. Lastly, multi-agent system inspired approaches may be more broadly useful in tackling other complex combinatorial search problems in biology.


Author(s):  
Carl A. Denard ◽  
Chelsea Paresi ◽  
Rasha Yaghi ◽  
Natalie McGinnis ◽  
Zachary Bennett ◽  
...  

2020 ◽  
Vol 65 ◽  
pp. 96-101 ◽  
Author(s):  
Vickery L Arcus ◽  
Marc W van der Kamp ◽  
Christopher R Pudney ◽  
Adrian J Mulholland

2020 ◽  
Vol 59 ◽  
pp. 147-154 ◽  
Author(s):  
Lianet Noda-Garcia ◽  
Dan S. Tawfik

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