Detailed Information on Publication Record
2014
Maximizing the Efficiency of Multi-enzyme Process by Stoichiometry Optimization.
DVOŘÁK, Pavel, Nagendra Prasad KURUMBANG, Jaroslav BENDL, Jan BREZOVSKÝ, Zbyněk PROKOP et. al.Basic information
Original name
Maximizing the Efficiency of Multi-enzyme Process by Stoichiometry Optimization.
Authors
DVOŘÁK, Pavel (203 Czech Republic, belonging to the institution), Nagendra Prasad KURUMBANG (524 Nepal, belonging to the institution), Jaroslav BENDL (203 Czech Republic, belonging to the institution), Jan BREZOVSKÝ (203 Czech Republic, belonging to the institution), Zbyněk PROKOP (203 Czech Republic, belonging to the institution) and Jiří DAMBORSKÝ (203 Czech Republic, guarantor, belonging to the institution)
Edition
ChemBioChem, WEINHEIM, WILEY-VCH, 2014, 1439-4227
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10600 1.6 Biological sciences
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 3.088
RIV identification code
RIV/00216224:14310/14:00074203
Organization unit
Faculty of Science
UT WoS
000341586100007
Keywords in English
biocatalysis; engineered enzymes
Tags
International impact, Reviewed
Změněno: 21/3/2017 07:35, prof. Mgr. Jiří Damborský, Dr.
Abstract
V originále
Multi-enzyme processes represent an important area of biocatalysis. Their efficiency can be enhanced by optimization of biocatalysts’ stoichiometry. Here we present a workflow for maximizing the efficiency of a three-enzyme system catalysing a five-step chemical conversion. Kinetic models of pathways featuring either wild-type or engineered enzymes were built and the enzyme stoichiometry of each pathway was optimized. Mathematical modelling and one-pot multi-enzyme laboratory experiments provided detailed insights into pathway dynamics, enabled the selection of suitable engineered enzyme and afforded high efficiency while minimizing biocatalyst loadings. The optimizing of stoichiometry in a pathway with engineered enzyme reduced the total biocatalyst load by an impressive 56 %. Our new workflow represents a broadly applicable strategy for optimizing multi-enzyme processes.
Links
EE2.3.30.0037, research and development project |
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GAP503/12/0572, research and development project |
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