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Rebecca Goss
Rebecca Goss
其他姓名Rebecca JM Goss, RJM Goss, Rebecca J Goss
Professor of Biological and Organic Chemistry
在 st-andrews.ac.uk 的电子邮件经过验证
标题
引用次数
引用次数
年份
The saponins–polar isoprenoids with important and diverse biological activities
A Osbourn, RJM Goss, RA Field
Natural product reports 28 (7), 1261-1268, 2011
3232011
Antimicrobial nucleoside antibiotics targeting cell wall assembly: Recent advances in structure–function studies and nucleoside biosynthesis
M Winn, RJM Goss, K Kimura, TDH Bugg
Natural product reports 27 (2), 279-304, 2010
3192010
A mixed community of actinomycetes produce multiple antibiotics for the fungus farming ant Acromyrmex octospinosus
J Barke, RF Seipke, S Grüschow, D Heavens, N Drou, MJ Bibb, RJM Goss, ...
BMC biology 8, 1-10, 2010
2802010
Antiviral drug discovery: preparing for the next pandemic
CS Adamson, K Chibale, RJM Goss, M Jaspars, DJ Newman, ...
Chemical Society Reviews 50 (6), 3647-3655, 2021
2122021
A serine carboxypeptidase-like acyltransferase is required for synthesis of antimicrobial compounds and disease resistance in oats
ST Mugford, X Qi, S Bakht, L Hill, E Wegel, RK Hughes, K Papadopoulou, ...
The Plant Cell 21 (8), 2473-2484, 2009
1992009
A Single Streptomyces Symbiont Makes Multiple Antifungals to Support the Fungus Farming Ant Acromyrmex octospinosus
RF Seipke, J Barke, C Brearley, L Hill, DW Yu, RJM Goss, MI Hutchings
PLoS one 6 (8), e22028, 2011
1982011
A translational synthetic biology platform for rapid access to gram-scale quantities of novel drug-like molecules
J Reed, MJ Stephenson, K Miettinen, B Brouwer, A Leveau, P Brett, ...
Metabolic Engineering 42, 185-193, 2017
1822017
Gene expression enabling synthetic diversification of natural products: chemogenetic generation of pacidamycin analogs
AD Roy, S Grüschow, N Cairns, RJM Goss
Journal of the American Chemical Society 132 (35), 12243-12245, 2010
1732010
Prospecting for new bacterial metabolites: a glossary of approaches for inducing, activating and upregulating the biosynthesis of bacterial cryptic or silent natural products
JS Zarins-Tutt, TT Barberi, H Gao, A Mearns-Spragg, L Zhang, ...
Natural product reports 33 (1), 54-72, 2016
1522016
The generation of “unnatural” products: synthetic biology meets synthetic chemistry
RJM Goss, S Shankar, A Abou Fayad
Natural Product Reports 29 (8), 870-889, 2012
1122012
Scope and potential of halogenases in biosynthetic applications
DRM Smith, S Grüschow, RJM Goss
Current opinion in chemical biology 17 (2), 276-283, 2013
1062013
New pacidamycin antibiotics through precursor‐directed biosynthesis
S Grüschow, EJ Rackham, B Elkins, PLA Newill, LM Hill, RJM Goss
ChemBioChem 10 (2), 355-360, 2009
952009
Artificial intelligence for natural product drug discovery
MW Mullowney, KR Duncan, SS Elsayed, N Garg, JJJ van der Hooft, ...
Nature Reviews Drug Discovery 22 (11), 895-916, 2023
902023
Pacidamycin biosynthesis: identification and heterologous expression of the first uridyl peptide antibiotic gene cluster
EJ Rackham, S Grüschow, AE Ragab, S Dickens, RJM Goss
ChemBioChem 11 (12), 1700-1709, 2010
882010
A marine viral halogenase that iodinates diverse substrates
DS Gkotsi, H Ludewig, SV Sharma, JA Connolly, J Dhaliwal, Y Wang, ...
Nature chemistry 11 (12), 1091-1097, 2019
792019
Evidence that a novel thioesterase is responsible for polyketide chain release during biosynthesis of the polyether ionophore monensin
BM Harvey, H Hong, MA Jones, ZA Hughes‐Thomas, RM Goss, ...
ChemBioChem 7 (9), 1435-1442, 2006
742006
Halogenases: powerful tools for biocatalysis (mechanisms applications and scope)
DS Gkotsi, J Dhaliwal, MMW McLachlan, KR Mulholand, RJM Goss
Current Opinion in Chemical Biology 43, 119-126, 2018
712018
A convenient enzymatic synthesis of L-halotryptophans
RJM Goss, PLA Newill
Chemical communications, 4924-4925, 2006
712006
Halogenases: a palette of emerging opportunities for synthetic biology–synthetic chemistry and C–H functionalisation
C Crowe, S Molyneux, SV Sharma, Y Zhang, DS Gkotsi, H Connaris, ...
Chemical Society Reviews 50 (17), 9443-9481, 2021
692021
The First One-Pot Synthesis of l-7-Iodotryptophan from 7-Iodoindole and Serine, and an Improved Synthesis of Other l-7-Halotryptophans
DRM Smith, T Willemse, DS Gkotsi, W Schepens, BUW Maes, S Ballet, ...
Organic letters 16 (10), 2622-2625, 2014
672014
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