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H R Perkins

Showing results (21-30 of 69) with videos related to

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The Biochemical Journal|June 1, 1974
Peptidoglycan biosynthesis by preparations from Bacillus licheniformis: cross-linking of newly synthesized chains to preformed cell wallJ B Ward, H R Perkins
FEBS Letters|September 1, 1979
Deoxycholate enhancement of an intermediate of peptidoglycan synthesis in Micrococcus luteusS J Thorpe, H R Perkins
Journal of General Microbiology|December 1, 1985
The peptidoglycan of Neisseria gonorrhoeae, with or without O-acetyl groups, contains anhydro-muramyl residuesJ K Blundell, H R Perkins
European Journal of Biochemistry|July 31, 1990
Peptidoglycan cross-linking in Staphylococcus aureus. An apparent random polymerisation processM A Snowden, H R Perkins
Journal of General Microbiology|March 1, 1983
Peptidoglycan-degrading enzymes in ether-treated cells of Neisseria gonorrhoeaeS J Chapman, H R Perkins
Journal of General Microbiology|March 1, 1983
Degrees of O-acetylation and cross-linking of the peptidoglycan of Neisseria gonorrhoeae during growthA L Lear, H R Perkins
The Biochemical Journal|November 1, 1974
Membrane-bound DD-carboxypeptidases from Bacillus megaterium KM general properties, substrate specificity and sensitivity to penicillins, cephalosporins and peptide inhibitors of the activity at pH5T Mauriño, M Nieto, H R Perkins
European Journal of Biochemistry|May 2, 1977
The exchange reaction of peptides R-D-alanyl-D-alanine with D-[14C]alanine to R-D-alanyl-D-[14C]alanine and D-alanine, catalysed by the membranes of Streptococcus faecalis ATCC 9790J Coyette, J M Ghuysen, H R Perkins
The Biochemical Journal|January 1, 1972
Reversal by a specific peptide (diacetyl-alpha gamma-L-diaminobutyryl-D-alanyl-D-alanine) of vancomycin inhibition in intact bacteria and cell-free preparationsM Nieto, H R Perkins, P E Reynolds
European Journal of Biochemistry|September 15, 1975
Interaction between the exocellular DD-carboxypeptidase-transpeptidase from Streptomyces R61, substrate and beta-lactam antibiotics. A choice of modelsJ M Frère, J M Ghuysen, H R Perkins
Pageof 7

Showing results (21-30 of 69) with videos related to

Sort By:
Pageof 7
The Biochemical Journal|June 1, 1974
Peptidoglycan biosynthesis by preparations from Bacillus licheniformis: cross-linking of newly synthesized chains to preformed cell wallJ B Ward, H R Perkins
FEBS Letters|September 1, 1979
Deoxycholate enhancement of an intermediate of peptidoglycan synthesis in Micrococcus luteusS J Thorpe, H R Perkins
Journal of General Microbiology|December 1, 1985
The peptidoglycan of Neisseria gonorrhoeae, with or without O-acetyl groups, contains anhydro-muramyl residuesJ K Blundell, H R Perkins
European Journal of Biochemistry|July 31, 1990
Peptidoglycan cross-linking in Staphylococcus aureus. An apparent random polymerisation processM A Snowden, H R Perkins
Journal of General Microbiology|March 1, 1983
Peptidoglycan-degrading enzymes in ether-treated cells of Neisseria gonorrhoeaeS J Chapman, H R Perkins
Journal of General Microbiology|March 1, 1983
Degrees of O-acetylation and cross-linking of the peptidoglycan of Neisseria gonorrhoeae during growthA L Lear, H R Perkins
The Biochemical Journal|November 1, 1974
Membrane-bound DD-carboxypeptidases from Bacillus megaterium KM general properties, substrate specificity and sensitivity to penicillins, cephalosporins and peptide inhibitors of the activity at pH5T Mauriño, M Nieto, H R Perkins
European Journal of Biochemistry|May 2, 1977
The exchange reaction of peptides R-D-alanyl-D-alanine with D-[14C]alanine to R-D-alanyl-D-[14C]alanine and D-alanine, catalysed by the membranes of Streptococcus faecalis ATCC 9790J Coyette, J M Ghuysen, H R Perkins
The Biochemical Journal|January 1, 1972
Reversal by a specific peptide (diacetyl-alpha gamma-L-diaminobutyryl-D-alanyl-D-alanine) of vancomycin inhibition in intact bacteria and cell-free preparationsM Nieto, H R Perkins, P E Reynolds
European Journal of Biochemistry|September 15, 1975
Interaction between the exocellular DD-carboxypeptidase-transpeptidase from Streptomyces R61, substrate and beta-lactam antibiotics. A choice of modelsJ M Frère, J M Ghuysen, H R Perkins
Pageof 7