Books "An Introduction to Enzyme and Coenzyme Chemistry" by T.D.H. Bugg Blackwells Science Ltd., Oxford, 1997, 247 pp

 

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2012

• Detection of Staphylococcus aureus cell walls by enzyme-linked immunoassay using antibodies prepared from a semi-synthetic peptidoglycan precursor S. Sandhu, J. A. Schouten, J. Thompson, M. Davis and T.D.H. Bugg, Analyst, 137, 1130-1136 (2012).
• Isolation of bacterial strains able to metabolise lignin from screening of environmental samples C.R. Taylor, E.M. Hardiman, M. Ahmad, P. Sainsbury, P.R. Norris, T.D.H. Bugg, Journal of Applied Microbiology, 113, 521-30 (2012).

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2011

• Bacterial cell wall assembly: still an attractive target T.D.H. Bugg, D. Braddick, C.G. Dowson and D. I. Roper, Trends in Biotechnology, 29, 167-173 (2011).
• The emerging role for bacteria in lignin degradation and bio-product formation T.D.H. Bugg, M. Ahmad, E.M. Hardiman and R. Singh, Current Opinion in Biotechnology, 22, 394-400 (2011)
• Identification of DypB from Rhodococcus jostii RHA1 as a Lignin Peroxidase M. Ahmad, J.N. Roberts, E.M. Hardiman, R. Singh, L.D. Eltis and T.D.H. Bugg, Biochemistry, 50, 5096–5107 (2011).
• Characterization of Dye-Decolorizing Peroxidases from Rhodococcus jostii RHA1 J. N. Roberts, R. Singh, J.C. Grigg, M.E.P. Murphy, T.D.H. Bugg, and L.D. Eltis, Biochemistry, 50, 5108–5119 (2011).
• Pathways for degradation of lignin in bacteria and fungi. T.D.H. Bugg, M. Ahmad, E. M. Hardiman and R. Rahmanpour. Natural Products Report, (2011), 28 (12), 1883 - 1896
• Indistinguishability and identifiability of kinetic models for the MurC reaction in peptidoglycan biosynthesis. J.G Hattersley, J. Pérez-Velázquez, M.J. Chappell, D. Bearup, D. Roper, C. Dowson, T.D.H. Bugg, N.D. Evans, Comput Methods Programs Biomed., 104., 70-80 (2011).

2010

• Biomimetic formation of 2-tropolones via dioxygenase-catalysed ring expansion of substituted cyclohexa-2,4-dienones M. Xin and T.D.H. Bugg,ChemBioChem, 11, 272-276 (2010).
• Antimicrobial nucleoside antibiotics targetting cell wall assembly: recent advances in structure-function studies and nucleoside biosynthesis M. Winn, R.J.M. Goss, K. Kimura, T.D.H. Bugg, Natural Product Reports, 27, 279-304 (2010).
• Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimicsA.E. Trunkfield, S.S. Gurcha, G.S. Besra, and T.D.H. Bugg, Bio-Organic and Medicinal Chemistry, 18, 2651-2663 (2010).
• Development of novel assays for lignin degradation: comparative analysis of bacterial and fungal lignin degraders M. Ahmad, C.R. Taylor, D. Pink, K. Burton, D. Eastwood, G.D. Bending and T.D.H. Bugg, Molecular Biosystems, 6, 815-821 (2010).
• Does abscisic acid affect strigolactone biosynthesis? J.A. López-Ráez, W. Kohlen, T. Charnikhova, P. Mulder, A. Undas, M.J. Sergeant, F. Verstappen, T.D.H. Bugg, A.J. Thompson, C. Ruyter-Spira, H. Bouwmeester, New Phytologist, 187, 343-354 (2010).

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2009

• Selective inhibition of carotenoid cleavage dioxygenases: phenotypic effects on shoot branching M. J. Sergeant, J-J. Li, C. Fox, N. Brookbank, D. Rea, T. D. H. Bugg, J. Biol. Chem. (2009), 284, 5257-5264.
• Investigation of acid/base catalysis in the extradiol and intradiol catechol dioxygenase reactions using a broad specificity mutant enzyme and model chemistry. M. Brivio, J. Schlosrich, M. Ahmad, C. Tolond and T. D. H. Bugg, Org. Biomol. Chem. (2009), 7, 1368-1373.
• Inhibition of lipid II:alanyl tRNA ligase MurM from Streptococcus pneumoniae by phosphonate and sulfonamide inhibitors E. Cressina, A.J. Lloyd, G. De Pascale, B.J. Mok, S. Caddick, D.I. Roper, C.G. Dowson, and T.D.H. Bugg, Bio-Org. Med. Chem, 17, 3443-3455 (2009).
• In vitro biosynthesis of bacterial peptidoglycan using D-Cys-containing precursors: fluorescent detection of transglycosylation and transpeptidation V. Vinatier, C.B. Blakey, D. Braddick, B.R.G. Johnson, S.D. Evans, and T.D.H. Bugg. Chem. Commun., 4037-4039 (2009).
• Oxygenases get to grips with polypeptides T.D.H. Bugg, Structure, 17, 913-914 (2009).
• Pseudomonas aeruginosa MurE amide ligase: enzyme kinetics and peptide inhibitor C. Paradis-Bleau, A. Lloyd, F. Sanschagrin, H. Maaroufi, T. Clarke, A. Blewett, C.G. Dowson, D.I. Roper, T.D.H. Bugg, and R.C. Levesque, Biochem. J., 421, 263-272 (2009).

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2008

• Kinetic Characterization of Lipid II-Ala: Alanyl-tRNA Ligase MurN from Streptococcus pneumoniae using semi-synthetic aminoacyl-lipid II substrates G. De Pascale, A. J. Lloyd, J. A. Schouten, A. M. Gilbey, D. I. Roper, C. G. Dowson & T. D. H. Bugg, Journal of Biological Chemistry (2008), 283, 34571-34579.
• Crystal Structure and Functional Assignment of YfaU, a Metal Ion Dependent Class II Aldolase from Escherichia coliK12. D. Rea, R. Hovington, J. F. Rakus, J. A. Gerlt, V. Fulop, T. D. H. Bugg, D. I. Roper, Biochemistry (2008), 47(38), 9955-9965.
• Evidence from Mechanistic Probes for Distinct Hydroperoxide Rearrangement Mechanisms in the Intradiol and Extradiol Catechol Dioxygenases. M. Xin, T. D. H. Bugg, Journal of the American Chemical Society (2008), 130(31), 10422-10430.
• Identification of a novel β-replacement reaction in the biosynthesis of 2,3-diaminobutyric acid in peptidylnucleoside mureidomycin A. W.-H. Lam, K. Rychli, T. D. H. Bugg, Organic & Biomolecular Chemistry (2008), 6(11), 1912-1917.
• Non-heme iron-dependent dioxygenases: unravelling catalytic mechanisms for complex enzymatic oxidations. T. D. H. Bugg, S. Ramaswamy, Current Opinion in Chemical Biology (2008), 12(2), 134-40.
• Evolution of peptidoglycan biosynthesis under the selective pressure of antibiotics in Gram-positive bacteria. J.-L. Mainardi, R. Villet, T. D. H. Bugg, C. Mayer, M. Arthur, FEMS Microbiology Reviews (2008), 32(2), 386-408.
• The biosynthesis of peptidoglycan lipid-linked intermediates. A. Bouhss, A. E. Trunkfield, T. D. H. Bugg, D. Mengin-Lecreulx, FEMS Microbiology Reviews (2008), 32(2), 208-233.
• Characterization of tRNA-dependent Peptide Bond Formation by MurM in the Synthesis of Streptococcus pneumoniae Peptidoglycan. A. J. Lloyd, A. M. Gilbey, A. M. Blewett, G. De Pascale, A. El Zoeiby, R. C. Levesque, A. C. Catherwood, A. Tomasz, T. D. H, Bugg, D. I. Roper, C. G. Dowson, Journal of Biological Chemistry (2008), 283(10), 6402-6417.
• Synthesis of gem-difluorinated nucleoside analogues of the liposidomycins and evaluation as MraY inhibitors. X.-H. Xu, A. E. Trunkfield, T. D. H. Bugg, F.-L. Qing, Organic & Biomolecular Chemistry (2008), 6(1), 157-161.
• Catalytic promiscuity in the alpha/beta-hydrolase superfamily: hydroxamic acid formation, C--C bond formation, ester and thioester hydrolysis in the C--C hydrolase family.  C. Li, M. Hassler, T. D. H. Bugg, ChemBioChem (2008), 9(1), 71-76.
• Native E. coli inner membrane incorporation in solid-supported lipid bilayer membranes. C. E. Dodd, B. R. G. Johnson, L. J. C. Jeuken, T. D. H. Bugg, R. J. Bushby, S. D. Evans, Biointerphases (2008), 3(2), FA59-FA67.

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2007

• Structure and Mechanism of HpcH: A Metal Ion Dependent Class II Aldolase from the Homoprotocatechuate Degradation Pathway of Escherichia coli. D. Rea, V. Fueloep, T. D. H. Bugg, D. I. Roper, Journal of Molecular Biology (2007), 373(4), 866-876.
• Adenosine phosphonate inhibitors of lipid II: Alanyl tRNA ligase MurM from Streptococcus pneumoniae. E. Cressina, A. J. Lloyd, G. De Pascale, D. I. Roper, C. Dowson, T. D. H. Bugg, Bioorganic & Medicinal Chemistry Letters (2007), 17(16), 4654-4656.
• Investigation of a general base mechanism for ester hydrolysis in C-C hydrolase enzymes of the α/β-hydrolase superfamily: a novel mechanism for the serine catalytic triad. J.–J. Li, T. D. H. Bugg, Organic & Biomolecular Chemistry(2007), 5(3), 507-513.

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2006

• Directed evolution of a non-heme-iron-dependent extradiol catechol dioxygenase: identification of mutants with intradiol oxidative cleavage activity. J. Schlosrich, K. L. Eley, P. J. Crowley, T. D. H. Bugg, ChemBioChem (2006), 7(12), 1899-1908.
• Fluorescent reagents for in vitro studies of lipid-linked steps of bacterial peptidoglycan biosynthesis: derivatives of UDPMurNAc-pentapeptide containing D-cysteine at position 4 or 5. J. A. Schouten, S. Bagga, A. J. Lloyd, G. de Pascale, C. G. Dowson, D. I. Roper, T. D. H. Bugg, Molecular BioSystems (2006), 2(10), 484-491.
• Catalytic role for arginine 188 in the C-C hydrolase catalytic mechanism for Escherichia coli MhpC and Burkholderia xenovorans LB400 BphD. C. Li, J.-J. Li, M. G. Montgomery, S. P. Wood, T. D. H. Bugg, Biochemistry (2006), 45(41), 12470-12479.
• Evidence for a gem-Diol Reaction Intermediate in Bacterial C-C Hydrolase Enzymes BphD and MhpC from 13C NMR Spectroscopy. J.-J. Li, C. Li, C. A. Blindauer, T. D. H. Bugg, Biochemistry (2006), 45(41), 12461-12469.
• Phospho-MurNAc-pentapeptide translocase (MraY) as a target for antibacterial agents and antibacterial proteins. T. D. H. Bugg, A. J. Lloyd, D. I. Roper, Infectious Disorders: Drug Targets (2006), 6(2), 85-106.
• Selection of peptide inhibitors against the Pseudomonas aeruginosa MurD cell wall enzyme. C. Paradis-Bleau, M. Beaumont, L. Boudreault, A. Lloyd, F. Sanschagrin, T. D. H. Bugg, R. C. Levesque, Peptides (2006), 27(7), 1693-1700.
• Antibiotic action and peptidoglycan formation on tethered lipid bilayer membranes. M. J. Spencelayh, Y. Cheng, R. J. Bushby, T. D. H. Bugg, J.-J. Li, P. J. F. Henderson, J. O'Reilly, S. D. Evans, Angewandte Chemie, (2006), 45(13), 2111-2116.
• Arene cis-dihydrodiol formation: from biology to application. D. R. Boyd, T. D. H. Bugg, Organic & Biomolecular Chemistry (2006), 4(2), 181-192.
• Interaction of the transmembrane domain of lysis protein E from bacteriophage phiX174 with bacterial translocase MraY and peptidyl-prolyl isomerase SlyD. S, Mendel, J. M. Holbourn, J. A. Schouten, T. D. H. Bugg Microbiology (2006), 152(10), 2959-67.

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2005

• Expression, purification and preliminary crystallographic analysis of 2,4-dihydroxy-hepta-2-ene-1,7-dioate aldolase (HpcH) from Escherichia coliC. D. Rea, V. Fulop, T. D. H. Bugg, D. I. Roper, Acta Crystallographica, Section F: Structural Biology and Crystallization Communications (2005), F61(9), 821-824.
• Lactone synthesis activity in a site-directed mutant of an extradiol catechol dioxygenase enzyme. S. Mendel, A. Arndt, T. D. H. Bugg, Chemical Communications (2005), (5), 666-668.
• The Structure of the C-C Bond Hydrolase MhpC Provides Insights into its Catalytic Mechanism. G. Dunn, M. G. Montgomery, F. Mohammed, A. Coker,J. B. Cooper, T. Robertson, J.-L. Garcia, T. D. H. Bugg, S. P. Wood, Journal of Molecular Biology (2005), 346(1), 253-265.
• Catalytic Mechanism of C-C Hydrolase MhpC from Escherichia coli: Kinetic Analysis of His263 and Ser110 Site-directed Mutants. C. Li, M. G. Montgomery, F. Mohammed, J.-J. Li, S. P. Wood, T. D. H. Bugg, Journal of Molecular Biology (2005), 346(1), 241-251.
• Stereochemistry of the reaction catalysed by 2-hydroxy-6-keto-6-phenyl-hexa-2,4-dienoic acid 5,6-hydrolase (BphD). J.-J. Li, T. D. H. Bugg,Chemical Communications (2005), (1), 130-132.
• Regulation and manipulation of the biosynthesis of abscisic acid, including the supply of xanthophyll precursors. I. B. Taylor, T. Sonneveld, T. D. H. Bugg, A. J. Thompson, Journal of Plant Growth Regulation (2005), 24(4), 253-273.

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2004

• Synthetic 6-aryl-2-hydroxy-6-ketohexa-2,4-dienoic acid substrates for C-C hydrolase BphD: investigation of a general base catalytic mechanism.D. M. Speare, S. M. Fleming, M. N. Beckett, J.-J. Li, T. D. H, Bugg, Organic & Biomolecular Chemistry (2004), 2(20), 2942-2950.
• Acid-Base Catalysis in the Extradiol Catechol Dioxygenase Reaction Mechanism: Site-Directed Mutagenesis of His-115 and His -179 in Escherichia coli 2,3-Dihydroxyphenylpropionate 1,2-Dioxygenase (MhpB). S. Mendel, A. Arndt, T. D. H. Bugg, Biochemistry (2004), 43(42), 13390-13396.
• Diverse catalytic activities in the αβ-hydrolase family of enzymes: activation of H₂O, HCN, H₂O₂, and O₂. T. D. H. Bugg, Bioorganic Chemistry (2004), 32(5), 367-375.
• Phospho-N-acetyl-muramyl-pentapeptide translocase from Escherichia coli: catalytic role of conserved aspartic acid residues. A. J. Lloyd, P. E. Brandish, A. M. Gilbey, T. D. H. Bugg, Journal of Bacteriology (2004), 186(6), 1747-1757.
• Expression, purification, crystallization and preliminary characterization of uridine 5'-diphospho-N-acetylmuramoyl l-alanyl-d-glutamate:lysine ligase (MurE) from Streptococcus pneumoniae 110K/70. A. M. Blewett, A. J. Lloyd, A. Echalier, V. Fueloep, C. G. Dowson, T. D. H. Bugg, D. I. Roper,Acta Crystallographica, Section D: Biological Crystallography (2004), D60(2), 359-361.
• A fluorescent analogue of UDP-N-acetylglucosamine: application for FRET assay of peptidoglycan translocase II (MurG). J.-J. Li, T. D. H. Bugg,Chemical Communications (2004), 2), 182-183.

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2003

• Multivalent Conjugates of Poly-g -D-glutamic Acid from Bacillus licheniformis with Antibody F(ab') and Glycopeptide Ligands. E. J. Prodhomme, A. L. Tutt, M. J. Glennie, T. D. H. Bugg, Bioconjugate Chemistry (2003), 14(6), 1148-1155.
• Dioxygenase enzymes: catalytic mechanisms and chemical models. T. D. H. Bugg, Tetrahedron (2003), 59(36), 7075-7101.
• Synthesis and activity of 5'-Uridinyl dipeptide analogues mimicking the amino terminal peptide chain of nucleoside antibiotic mureidomycin A. N. I.Howard, T. D. H. Bugg, Bioorganic & Medicinal Chemistry (2003), 11(14), 3083-3099.
• Stereochemical and mechanistic aspects of dioxygenase-catalyzed benzylic hydroxylation of indene and chroman substrates. D. R. Boyd, N. D. Sharma, N. I. Bowers, R. Boyle, J. S. Harrison, K. Lee, T. D. H. Bugg, D. T. Gibson, Organic & Biomolecular Chemistry (2003), 1(8), 1298-1307.
• A density functional investigation of the extradiol cleavage mechanism in non-heme iron catechol dioxygenases. R. J. Deeth, T. D. H. Bugg, Journal of Biological Inorganic Chemistry (2003), 8(4), 409-418.
• Recent advances in antimicrobial nucleoside antibiotics targeting cell wall biosynthesis. K.-I. Kimura, T. D. H. Bugg, Natural Product Reports (2003), 20(2), 252-273.

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2002

• 2-Hydroxy-6-keto-nona-2,4-diene 1,9-dioic acid 5,6-hydrolase: evidence from ¹⁸O isotope exchange for gem-diol intermediate. T. D. H. Bugg, S. M. Fleming, T. A. Robertson, G. J. Langley, Methods in Enzymology (2002), 354, 106-118.
• Enzyme Assays, 2nd Edition Edited by R. Eisenthal and M. J. Hanson. T. D. H. Bugg, University of Warwick, UK. Natural Product Reports (2002), 19(5), 673.
• Hammett analysis of a C-C hydrolase-catalysed reaction using synthetic 6-aryl-2-hydroxy-6-ketohexa-2,4-dienoic acid substrates. D. M. Speare, P. Olf, T. D. H. Bugg, Chemical Communications (2002), (20), 2304-2305.
• Biological Properties of N-Acyl and N-Haloacetyl Neuraminic Acids: Processing by Enzymes of Sialic Acid Metabolism, and Interaction with Influenza Virus. A. J. Humphrey, C. Fremann, P. Critchley, Y. Malykh, R. Schauer, T. D. H. Bugg, Bioorganic & Medicinal Chemistry (2002), 10(10), 3175-3185.
• Directed evolution of intradiol and extradiol catechol dioxygenases. K. Eley, T. D. H. Bugg, P. Crowley, Abstracts of Papers, 224th ACS National Meeting, Boston, MA, United States, August 18-22, 2002 (2002), BIOL-043.
• Thioester analogues of peptidoglycan fragment MurNAc-L-Ala-g -D-Glu as substrates for peptidoglycan hydrolase MurNAc-L-Ala amidase. R. L. Harding, J. Henshaw, J. Tilling, T. D. H. Bugg, Journal of the Chemical Society, Perkin Transactions 1 (2002), (14), 1714-1722.

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 2001

• Extradiol Oxidative Cleavage of Catechols by Ferrous and Ferric Complexes of 1,4,7-Triazacyclononane: Insight into the Mechanism of the Extradiol Catechol Dioxygenases. G. Lin, G. Reid, T. D. H. Bugg, Journal of the American Chemical Society (2001), 123(21), 5030-5039.
• Oxygenases: mechanisms and structural motifs for O₂ activation. T. D. H. Bugg, Current Opinion in Chemical Biology (2001), 5(5), 550-555.
• Enhanced acid stability of a reduced nicotinamide adenine dinucleotide (NADH) analogue. P. H. Hentall, N. Flowers, T. D. H. Bugg, Chemical Communications (2001), (20), 2098-2099.
• The development of mechanistic enzymology in the 20th century. T. D. H. Bugg, Natural Product Reports (2001), 18(5), 465-493.
• Enzymes: Biochemistry, Biotechnology, Clinical Chemistry, by Trevor Palmer. T. D. H. Bugg, Natural Product Reports (2001), 18(4), 460.
• Solving the riddle of the intradiol and extradiol catechol dioxygenases: how do enzymes control hydroperoxide rearrangements? T. D. H. Bugg, G. Lin, Chemical Communications (2001), (11), 941-952.
• Solvolytic C-C Cleavage Reaction of 6-Acetoxycyclohexa-2,4-dienones: Mechanistic Implications for the Intradiol Catechol Dioxygenases. K. L.Eley, P. J. Crowley, T. D. H. Bugg, Journal of Organic Chemistry (2001), 66(6), 2091-2097.
• Mechanistic studies of hydrolase enzymes on the aromatic degradation pathways of Escherichia coli. D. M. Speare, T. D. H. Bugg, Abstracts of Papers, 222nd ACS National Meeting, Chicago, IL, United States, August 26-30, 2001 (2001), BIOL-221.
• Synthesis of novel inhibitors of phospho-N-acetylmuramylpentapeptide translocase (mraY). N. I. Howard, T. D. H. Bugg, Abstracts of Papers, 222nd ACS National Meeting, Chicago, IL, United States, August 26-30, 2001 (2001), BIOL-109.

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2000

• Catalytic Mechanism of a C-C Hydrolase Enzyme: Evidence for a Gem-Diol Intermediate, Not an Acyl Enzyme. S. M. Fleming, T. A. Robertson, G. J. Langley, T. D. H. Bugg, Biochemistry (2000), 39(6), 1522-1531.
• Enzymatic Breakdown of Poly-g-D-glutamic Acid in Bacillus licheniformis: Identification of a Polyglutamyl g -Hydrolase Enzyme. E. C. King, A. J. Blacker, T. D. H. Bugg, Biomacromolecules (2000), 1(1), 75-83.
• Use of trityl thiol for stereoselective thioester synthesis: a new preparation of (S)-thiolactic acid. R. L. Harding, T. D. H. Bugg, Tetrahedron Letters(2000), 41(15), 2729-2731.
• A biomimetic model reaction for the extradiol catechol dioxygenases. G. Lin, T. D. H. Bugg, G. Reid, Chemical Communications (2000), (13), 1119-1120.
• Elucidation of the catalytic mechanisms of the non-haem iron-dependent catechol dioxygenases: synthesis of carba-analogues for hydroperoxide reaction intermediates. C. J. Winfield, Z. Al-Mahrizy, M. Gravestock, T. D. H. Bugg, Journal of the Chemical Society, Perkin Transactions 1 (2000), (19), 3277-3289.

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1999

• Bacterial peptidoglycan biosynthesis and its inhibition. T. D. H. Bugg, Comprehensive Natural Products Chemistry (1999), 3 41-294
• Structure-function studies on nucleoside antibiotic mureidomycin A: synthesis of 5'-functionalized uridine models. C. A. Gentle, S. A. Harrison, M. Inukai, T. D. H. Bugg, Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1999), (10), 1287-1294.
• Role of the enamide linkage of nucleoside antibiotic mureidomycin A: synthesis and reactivity of enamide-containing analogues. C. A. Gentle, T. D. H. Bugg, Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1999), (10), 1279-1286.

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1998

• Substrate selectivity and biochemical properties of 4-hydroxy-2-keto-pentanoic acid aldolase from Escherichia coli. J. R. Pollard, D. Rialland, T. D. H. Bugg, Applied and Environmental Microbiology (1998), 64(10), 4093-4094.
• Enzymic cleavage of aromatic rings: mechanistic aspects of the catechol dioxygenases and later enzymes of bacterial oxidative cleavage pathways. T. D. H. Bugg, C. J. Winfield, Natural Product Reports (1998), 15(5), 513-530.
• Covalent modification in aqueous solution of poly-g -D-glutamic acid from Bacillus licheniformis. E. C. King, W. J. Watkins, A. J. Blacker, T. D. H. Bugg, Journal of Polymer Science, Part A: Polymer Chemistry (1998), 36(12), 1995-1999.
• Purification, characterization and reaction mechanism of monofunctional 2-hydroxypentadienoic acid hydratase from Escherichia coli. J. R. Pollard, T. D. H. Bugg, European Journal of Biochemistry (1998), 251(1/2), 98-106.
• Aminoalkylphosphinate inhibitors of D-Ala-D-Ala adding enzyme. D. J. Miller, S. M. Hammond, D. Anderluzzi, T. D. H. Bugg, Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1998), (1), 131-142.

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1997

• Pre-Steady-State Kinetic Analysis of 2-Hydroxy-6-keto-nona-2,4-diene-1,9-dioic Acid 5,6-Hydrolase: Kinetic Evidence for Enol/Keto Tautomerization. I. M. Henderson, T. D. H. Bugg, Biochemistry (1997), 36(40), 12252-12258.
• Purification, Characterization, and Stereochemical Analysis of a C-C Hydrolase: 2-Hydroxy-6-keto-nona-2,4-diene-1,9-Dioic Acid 5,6-Hydrolase.W. W. Y. Lam, T. D. H. Bugg, Biochemistry (1997), 36(40), 12242-12251.
• Chemical and biochemical properties of 2-hydroxypentadienoic acid, a homolog of enolpyruvic acid. J. R. Pollard, I. M. Henderson, T. D. H. Bugg,Chemical Communications (1997), (19), 1885-1886.
• Exploring the catalytic mechanism of the extradiol catechol dioxygenases. T. D. H. Bugg, J. Sanvoisin, E. L. Spence, Biochemical Society Transactions(1997), 25(1), 81-85.
• Regiospecific ester hydrolysis by orange peel esterase: an undergraduate experiment. T. D. H. Bugg, A. M. Lewin, E. R. Catlin, Journal of Chemical Education (1997), 74(1), 105-107.

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1996

• Catechol dioxygenases from Escherichia coli (MhpB) and Alcaligenes eutrophus (MpcI): sequence analysis and biochemical properties of a third family of extradiol dioxygenases. E. L. Spence, M. Kawamukai, J. Sanvoisin, H. Braven, T. D. H. Bugg, Journal of Bacteriology (1996), 178(17), 5249-5256.
• Cis-Trans Isomerization of a Cyclopropyl Radical Trap Catalyzed by Extradiol Catechol Dioxygenases: Evidence for a Semiquinone Intermediate.E. L. Spence, G. J. Langley, T. D. H. Bugg, Journal of the American Chemical Society (1996), 118(35), 8336-83
• Modes of action of tunicamycin, liposidomycin B, and mureidomycin A: inhibition of phospho-N-acetylmuramyl-pentapeptide translocase fromEscherichia coli. P. E. Brandish, K.-I. Kimura, M. Inukai, R. Southgate, J. T. Lonsdale, T. D. H. Bugg, Antimicrobial Agents and Chemotherapy (1996), 40(7), 1640-1644.
• Slow binding inhibition of phospho-N-acetylmuramyl-pentapeptide-translocase (Escherichia coli) by mureidomycin A. P. E. Brandish, M. K.Burnham, J. T. Lonsdale, R. Southgate, M. Inukai, T. D. H. Bugg, Journal of Biological Chemistry (1996), 271(13), 7609-14.

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