RetroBioCat Database: A Platform for Collaborative Curation and Automated Meta-Analysis of Biocatalysis Data

被引:19
作者
Finnigan, William [1 ]
Lubberink, Max [1 ,2 ]
Hepworth, Lorna J. [1 ]
Citoler, Joan [1 ]
Mattey, Ashley P. [1 ]
Ford, Grayson J. [1 ]
Sangster, Jack [1 ]
Cosgrove, Sebastian C. [1 ,3 ]
da Costa, Bruna Zucoloto [1 ]
Heath, Rachel S. [1 ]
Thorpe, Thomas W. [1 ,4 ]
Yu, Yuqi [1 ]
Flitsch, Sabine L. [1 ]
Turner, Nicholas J. [1 ]
机构
[1] Univ Manchester, Manchester Inst Biotechnol, Dept Chem, 131 Princess St, Manchester M1 7DN, England
[2] Wageningen Food & Biobased Res, POB 17, NL-6700AA Wageningen, Netherlands
[3] Keele Univ, Sch Chem & Phys Sci, Lennard Jones Lab, Keele ST5 5BG, Staffs, England
[4] Univ Edinburgh, Inst Quantitat Biol Biochem & Biotechnol, Sch Biol Sci, Kings Bldg,Alexander Crum Brown Rd, Edinburgh EH9 3FF, Midlothian, Scotland
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
biocatalysis; database; enzyme selection; visualization; synthesis planning; ENZYMES;
D O I
10.1021/acscatal.3c01418
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Despite the increasinguseof biocatalysis for organic synthesis, there are currently no databasesthat adequately capture synthetic biotransformations. The lack ofa biocatalysis database prevents accelerating biocatalyst characterizationefforts from being leveraged to quickly identify candidate enzymesfor reactions or cascades, slowing their development. The RetroBioCatDatabase (available at retrobiocat.com) addresses this gap by capturing information on synthetic biotransformationsand providing an analysis platform that allows biocatalysis data tobe searched and explored through a range of highly interactive datavisualization tools. This database makes it simple to explore availableenzymes, their substrate scopes, and how characterized enzymes arerelated to each other and the wider sequence space. Data entry isfacilitated through an openly accessible curation platform, featuringautomated tools to accelerate the process. The RetroBioCat Databasedemocratizes biocatalysis knowledge and has the potential to acceleratebiocatalytic reaction development, making it a valuable resource forthe community.
引用
收藏
页码:11771 / 11780
页数:10
相关论文
共 46 条
[41]   Carboxylic acid reductase enzymes (CARs) [J].
Winkler, Margit .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2018, 43 :23-29
[42]   Discovery, characterization and engineering of ligases for amide synthesis [J].
Winn, Michael ;
Rowlinson, Michael ;
Wang, Fanghua ;
Bering, Luis ;
Francis, Daniel ;
Levy, Colin ;
Micklefield, Jason .
NATURE, 2021, 593 (7859) :391-+
[43]   Biocatalysis: Enzymatic Synthesis for Industrial Applications [J].
Wu, Shuke ;
Snajdrova, Radka ;
Moore, Jeffrey C. ;
Baldenius, Kai ;
Bornscheuer, Uwe T. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (01) :88-119
[44]   The Time and Place for Nature in Drug Discovery [J].
Young, Robert J. ;
Flitsch, Sabine L. ;
Grigalunas, Michael ;
Leeson, Paul D. ;
Quinn, Ronald J. ;
Turner, Nicholas J. ;
Waldmann, Herbert .
JACS AU, 2022, 2 (11) :2400-2416
[45]   The EFI Web Resource for Genomic Enzymology Tools: Leveraging Protein, Genome, and Metagenome Databases to Discover Novel Enzymes and Metabolic Pathways [J].
Zallot, Remi ;
Oberg, Nils ;
Gerlt, John A. .
BIOCHEMISTRY, 2019, 58 (41) :4169-4182
[46]   Enantioselective Biocatalytic Reduction of 2H-1,4-Benzoxazines Using Imine Reductases [J].
Zumbraegel, Nadine ;
Machui, Paul ;
Nonnhoff, Jannis ;
Groeger, Harald .
JOURNAL OF ORGANIC CHEMISTRY, 2019, 84 (03) :1440-1447