muramidase and 1-2-cyclohexanedione

muramidase has been researched along with 1-2-cyclohexanedione* in 1 studies

Other Studies

1 other study(ies) available for muramidase and 1-2-cyclohexanedione

Article	Year
Obviation of destructive action of 0.2 M NaOH on proteins during arginine modification with cyclohexanedione by use of 0.1 M triethylamine as solvent. Biochimica et biophysica acta, 1971, Nov-19, Volume: 251, Issue:2 The use of 0.2 M NaOH as a solvent for modification of arginine residues by 1,2-cyclohexanedione in disulfide containing proteins is destructive to the disulfide bonds. Modification can be conveniently done in 0.1 M triethylamine (pH 10.9) without any deleterious effect. Lysozyme was found to retain all its enzymic activity in 0.1 M triethylamine (pH 10.9) whereas complete loss of activity took place in 0.2 M NaOH. Topics: Arginine; Cyclohexanones; Disulfides; Ethylamines; Humans; Hydrogen-Ion Concentration; Immunoglobulin G; Indicators and Reagents; Kinetics; Lactalbumin; Muramidase; Proteins; Serum Albumin, Bovine; Sodium Hydroxide; Solvents	1971

Article

Year

Obviation of destructive action of 0.2 M NaOH on proteins during arginine modification with cyclohexanedione by use of 0.1 M triethylamine as solvent.

Biochimica et biophysica acta, 1971, Nov-19, Volume: 251, Issue:2

The use of 0.2 M NaOH as a solvent for modification of arginine residues by 1,2-cyclohexanedione in disulfide containing proteins is destructive to the disulfide bonds. Modification can be conveniently done in 0.1 M triethylamine (pH 10.9) without any deleterious effect. Lysozyme was found to retain all its enzymic activity in 0.1 M triethylamine (pH 10.9) whereas complete loss of activity took place in 0.2 M NaOH.

Topics: Arginine; Cyclohexanones; Disulfides; Ethylamines; Humans; Hydrogen-Ion Concentration; Immunoglobulin G; Indicators and Reagents; Kinetics; Lactalbumin; Muramidase; Proteins; Serum Albumin, Bovine; Sodium Hydroxide; Solvents

1971