Formation of peptide bonds by carboxypeptidase c from orange leaves. 1991

D Steinke, and A Schwarz, and C Wandrey, and M R Kula
Institut für Enzymtechnologie, Heinrich Heine Universität Düsseldorf, Jülich, FRG.

Carboxypeptidase c partially purified from orange leaves was studied as a catalyst for enzymatic peptide synthesis. Various N-protected ester- and nucleophile compounds were evaluated in order to determine the substrate specificity. For further characterization of the synthetic reaction, optimum pH and the influence of the N-terminal protecting group were studied. Kinetic investigations revealed considerable differences in Km and Vmax for the nucleophile when the N-terminal protecting group of the substrate was varied.

UI MeSH Term Description Entries
D007202 Indicators and Reagents Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant & Hackh's Chemical Dictionary, 5th ed, p301, p499) Indicator,Reagent,Reagents,Indicators,Reagents and Indicators
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D009842 Oligopeptides Peptides composed of between two and twelve amino acids. Oligopeptide
D010455 Peptides Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are considered to be larger versions of peptides that can form into complex structures such as ENZYMES and RECEPTORS. Peptide,Polypeptide,Polypeptides
D010944 Plants Multicellular, eukaryotic life forms of kingdom Plantae. Plants acquired chloroplasts by direct endosymbiosis of CYANOBACTERIA. They are characterized by a mainly photosynthetic mode of nutrition; essentially unlimited growth at localized regions of cell divisions (MERISTEMS); cellulose within cells providing rigidity; the absence of organs of locomotion; absence of nervous and sensory systems; and an alternation of haploid and diploid generations. It is a non-taxonomical term most often referring to LAND PLANTS. In broad sense it includes RHODOPHYTA and GLAUCOPHYTA along with VIRIDIPLANTAE. Plant
D002268 Carboxypeptidases Enzymes that act at a free C-terminus of a polypeptide to liberate a single amino acid residue. Carboxypeptidase
D004151 Dipeptides Peptides composed of two amino acid units. Dipeptide
D000595 Amino Acid Sequence The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION. Protein Structure, Primary,Amino Acid Sequences,Sequence, Amino Acid,Sequences, Amino Acid,Primary Protein Structure,Primary Protein Structures,Protein Structures, Primary,Structure, Primary Protein,Structures, Primary Protein
D013379 Substrate Specificity A characteristic feature of enzyme activity in relation to the kind of substrate on which the enzyme or catalytic molecule reacts. Specificities, Substrate,Specificity, Substrate,Substrate Specificities

Related Publications

D Steinke, and A Schwarz, and C Wandrey, and M R Kula
November 1971, Hoppe-Seyler's Zeitschrift fur physiologische Chemie,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
March 1972, European journal of biochemistry,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
October 1968, Hoppe-Seyler's Zeitschrift fur physiologische Chemie,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
November 1990, Enzyme and microbial technology,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
October 2002, Journal of the American Chemical Society,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
June 1990, Biotechnology and bioengineering,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
July 1970, European journal of biochemistry,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
July 2018, Chemical reviews,
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
May 2017, Dalton transactions (Cambridge, England : 2003),
D Steinke, and A Schwarz, and C Wandrey, and M R Kula
January 1974, Origins of life,
Copied contents to your clipboard!