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  • Title: Increase in thermostability of N-carbamyl-D-amino acid amidohydrolase on amino acid substitutions.
    Author: Ikenaka Y, Nanba H, Yajima K, Yamada Y, Takano M, Takahashi S.
    Journal: Biosci Biotechnol Biochem; 1998 Sep; 62(9):1668-71. PubMed ID: 9805366.
    Abstract:
    To improve the production of D-amino acids using an immobilized N-carbamyl-D-amino acid amidohydrolase, the enzyme gene of Agrobacterium sp. KNK712 was mutagenized randomly to increase its thermostability. The gene was inserted into M13mp19, mutagenized with hydroxylamine, ligated into pUC19 after restriction endonuclease digestion, and then used to transform Escherichia coli. The resultant transformants were screened by a newly developed colorimetric enzyme assay method, and the candidate colonies corresponding to red spots were separated from the master plates. Using cell-free extracts of these clones, the properties of the enzymes produced were investigated, it being proved that these enzymes had almost the same activity and improved thermostability by about 5 degrees C compared with those of the native enzyme. As found on enzyme gene analysis of these mutants, the 57th amino acid, histidine, of the enzyme was changed to tyrosine, or the 203rd amino acid, proline, to leucine or serine.
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