Molecular cloning and characterization of a rhamnogalacturonan acetylesterase from Aspergillus aculeatus. Synergism between rhamnogalacturonan degrading enzymes. 1995

S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
GeneSearch, Novo Nordisk A/S, Novo Allé, Bagsvaerd, Denmark.

A rhamnogalacturonan acetylesterase (RGAE) was purified to homogeneity from the filamentous fungus Aspergillus aculeatus, and the NH2-terminal amino acid sequence was determined. Full-length cDNAs encoding the enzyme were isolated from an A. aculeatus cDNA library using a polymerase chain reaction-generated product as a probe. The 936-base pair rha1 cDNA encodes a 250-residue precursor protein of 26,350 Da, including a 17-amino acid signal peptide. The rha1 cDNA was overexpressed in Aspergillus oryzae, a filamentous fungus that does not possess RGAE activity, and the recombinant enzyme was purified and characterized. Mass spectrometry of the native and recombinant RGAE revealed that the enzymes are heterogeneously glycosylated. In addition, the observed differences in their molecular masses, lectin binding patterns, and monosaccharide compositions indicate that the glycan moieties on the two enzymes are structurally different. The RGAE was shown to act in synergy with rhamnogalacturonase A as well as rhamnogalacturonase B from A. aculeatus in the degradation of apple pectin rhamnogalacturonan. RNA gel blot analyses indicate that the expression of rhamnogalacturonan degrading enzymes by A. acculeatus is regulated at the level of transcription and is subjected to carbon catabolite repression by glucose.

UI MeSH Term Description Entries
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
D008970 Molecular Weight The sum of the weight of all the atoms in a molecule. Molecular Weights,Weight, Molecular,Weights, Molecular
D010368 Pectins High molecular weight polysaccharides present in the cell walls of all plants. Pectins cement cell walls together. They are used as emulsifiers and stabilizers in the food industry. They have been tried for a variety of therapeutic uses including as antidiarrheals, where they are now generally considered ineffective, and in the treatment of hypercholesterolemia. Calcium Pectinate,Methoxy Pectin,Methoxylpectin,Methoxypectin,Pectin,Pectinic Acid,Zinc Pectinate,Pectin, Methoxy,Pectinate, Calcium,Pectinate, Zinc
D011994 Recombinant Proteins Proteins prepared by recombinant DNA technology. Biosynthetic Protein,Biosynthetic Proteins,DNA Recombinant Proteins,Recombinant Protein,Proteins, Biosynthetic,Proteins, Recombinant DNA,DNA Proteins, Recombinant,Protein, Biosynthetic,Protein, Recombinant,Proteins, DNA Recombinant,Proteins, Recombinant,Recombinant DNA Proteins,Recombinant Proteins, DNA
D003001 Cloning, Molecular The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells. Molecular Cloning
D004271 DNA, Fungal Deoxyribonucleic acid that makes up the genetic material of fungi. Fungal DNA
D005800 Genes, Fungal The functional hereditary units of FUNGI. Fungal Genes,Fungal Gene,Gene, Fungal
D005947 Glucose A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement. Dextrose,Anhydrous Dextrose,D-Glucose,Glucose Monohydrate,Glucose, (DL)-Isomer,Glucose, (alpha-D)-Isomer,Glucose, (beta-D)-Isomer,D Glucose,Dextrose, Anhydrous,Monohydrate, Glucose
D006031 Glycosylation The synthetic chemistry reaction or enzymatic reaction of adding carbohydrate or glycosyl groups. GLYCOSYLTRANSFERASES carry out the enzymatic glycosylation reactions. The spontaneous, non-enzymatic attachment of reducing sugars to free amino groups in proteins, lipids, or nucleic acids is called GLYCATION (see MAILLARD REACTION). Protein Glycosylation,Glycosylation, Protein
D000115 Acetylesterase An enzyme that catalyzes the conversion of acetate esters and water to alcohols and acetate. EC 3.1.1.6. Acetylase,Acetate Esterase,Acid Esterase,Esterase-17,Esterase 17,Esterase, Acetate,Esterase, Acid

Related Publications

S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
September 1998, Acta crystallographica. Section D, Biological crystallography,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
November 2020, Carbohydrate polymers,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
August 2002, Acta crystallographica. Section D, Biological crystallography,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
October 2014, Journal of microbiology and biotechnology,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
July 1997, Applied and environmental microbiology,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
January 1995, Current genetics,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
November 2010, Journal of molecular biology,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
June 1996, The Journal of biological chemistry,
S Kauppinen, and S Christgau, and L V Kofod, and T Halkier, and K Dörreich, and H Dalbøge
November 2012, Biochemistry. Biokhimiia,
Copied contents to your clipboard!