Xu Y, Liu S, Gao J, Hai Y
Biochemistry. 2024; 63(24):3348-3356.
PMID: 39641520
PMC: 11779795.
DOI: 10.1021/acs.biochem.4c00588.
Cao L, Zhang J, Chen J, Li M, Chen H, Wang C
Arch Microbiol. 2024; 206(9):390.
PMID: 39222088
DOI: 10.1007/s00203-024-04123-z.
Jain S, Ospina F, Hammer S
JACS Au. 2024; 4(6):2068-2080.
PMID: 38938808
PMC: 11200230.
DOI: 10.1021/jacsau.4c00247.
Almhjell P, Johnston K, Porter N, Kennemur J, Bhethanabotla V, Ducharme J
Nat Chem Biol. 2024; 20(8):1086-1093.
PMID: 38744987
PMC: 11288773.
DOI: 10.1038/s41589-024-01619-z.
Scheele R, Weber Y, Nintzel F, Herger M, Kaminski T, Hollfelder F
ACS Catal. 2024; 14(8):6259-6271.
PMID: 38660603
PMC: 11036396.
DOI: 10.1021/acscatal.4c00230.
The discovery of novel noncoding RNAs in 50 bacterial genomes.
Narunsky A, Higgs G, Torres B, Yu D, de Andrade G, Kavita K
Nucleic Acids Res. 2024; 52(9):5152-5165.
PMID: 38647067
PMC: 11109978.
DOI: 10.1093/nar/gkae248.
Neutron diffraction from a microgravity-grown crystal reveals the active site hydrogens of the internal aldimine form of tryptophan synthase.
Drago V, Devos J, Blakeley M, Forsyth V, Parks J, Kovalevsky A
Cell Rep Phys Sci. 2024; 5(2).
PMID: 38645802
PMC: 11027755.
DOI: 10.1016/j.xcrp.2024.101827.
Multiplexed Assessment of Promiscuous Non-Canonical Amino Acid Synthase Activity in a Pyridoxal Phosphate-Dependent Protein Family.
Zmich A, Perkins L, Bingman C, Acheson J, Buller A
ACS Catal. 2023; 13(17):11644-11655.
PMID: 37720819
PMC: 10501158.
DOI: 10.1021/acscatal.3c02498.
Engineered Biocatalytic Synthesis of β-N-Substituted-α-Amino Acids.
Villalona J, Higgins P, Buller A
Angew Chem Int Ed Engl. 2023; 62(43):e202311189.
PMID: 37625129
PMC: 10592029.
DOI: 10.1002/anie.202311189.
Stereoselective amino acid synthesis by synergistic photoredox-pyridoxal radical biocatalysis.
Cheng L, Li D, Mai B, Bo Z, Cheng L, Liu P
Science. 2023; 381(6656):444-451.
PMID: 37499030
PMC: 10444520.
DOI: 10.1126/science.adg2420.
Aqueous Flavin Photoredox Catalysis Drives Exclusive C3-Alkylation of Indolyl Radical Cations in Route to Unnatural Tryptophan Mimetics.
Immel J, Alghafli B, Rodriguez Ugalde A, Bloom S
Org Lett. 2023; 25(20):3818-3822.
PMID: 37191639
PMC: 11055211.
DOI: 10.1021/acs.orglett.3c01398.
Going Full Circle with Organocatalysis and Biocatalysis: The Latent Potential of Cofactor Mimics in Asymmetric Synthesis.
Murray J, Hodgson D, ODonoghue A
J Org Chem. 2023; 88(12):7619-7629.
PMID: 37126859
PMC: 10278144.
DOI: 10.1021/acs.joc.2c02747.
In vivo hypermutation and continuous evolution.
Molina R, Rix G, Mengiste A, Alvarez B, Seo D, Chen H
Nat Rev Methods Primers. 2023; 2.
PMID: 37073402
PMC: 10108624.
DOI: 10.1038/s43586-022-00130-w.
Chemoenzymatic Synthesis of Indole-Containing Acyloin Derivatives.
Alrashdi S, Casolari F, Alabed A, Kyeremeh K, Deng H
Molecules. 2023; 28(1).
PMID: 36615552
PMC: 9822442.
DOI: 10.3390/molecules28010354.
Biocatalytic Friedel-Crafts Reactions.
Leveson-Gower R, Roelfes G
ChemCatChem. 2023; 14(18):e202200636.
PMID: 36606067
PMC: 9804301.
DOI: 10.1002/cctc.202200636.
Substrate multiplexed protein engineering facilitates promiscuous biocatalytic synthesis.
McDonald A, Higgins P, Buller A
Nat Commun. 2022; 13(1):5242.
PMID: 36068220
PMC: 9448781.
DOI: 10.1038/s41467-022-32789-w.
Engineered Tryptophan Synthase Balances Equilibrium Effects and Fast Dynamic Effects.
Schafer J, Chen X, Schwartz S
ACS Catal. 2022; 12(2):913-922.
PMID: 35719741
PMC: 9202816.
DOI: 10.1021/acscatal.1c03913.
l-Serine Biosensor-Controlled Fermentative Production of l-Tryptophan Derivatives by .
Ferrer L, Elsaraf M, Mindt M, Wendisch V
Biology (Basel). 2022; 11(5).
PMID: 35625472
PMC: 9138238.
DOI: 10.3390/biology11050744.
Microgravity crystallization of perdeuterated tryptophan synthase for neutron diffraction.
Drago V, Devos J, Blakeley M, Forsyth V, Kovalevsky A, Schall C
NPJ Microgravity. 2022; 8(1):13.
PMID: 35508463
PMC: 9068912.
DOI: 10.1038/s41526-022-00199-3.
The Transformative Power of Biocatalysis in Convergent Synthesis.
Zetzsche L, Chakrabarty S, Narayan A
J Am Chem Soc. 2022; 144(12):5214-5225.
PMID: 35290055
PMC: 10082969.
DOI: 10.1021/jacs.2c00224.