Molecular cloning, sequence analysis, and in vitro expression of flavanone 3 beta-hydroxylase from Petunia hybrida

A cDNA encoding flavanone 3,6-hydroxylase was isolated from petals of Petunia hybrida. The open reading frame of the nearly full length cDNA coded for a 369-amino acid polypeptide with a calculated Mr of 41,466. The function of this nucleotide sequence was verified by comparison with amino acid sequ...

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Veröffentlicht in:The Journal of biological chemistry 1992-03, Vol.267 (8), p.5380-5387
Hauptverfasser: Britsch, L. (Biologisches Institut II der Universitat, Freiburg, Federal Republic of Germany), Ruhjnau-Brich, B, Forkmann, G
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Sprache:eng
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Zusammenfassung:A cDNA encoding flavanone 3,6-hydroxylase was isolated from petals of Petunia hybrida. The open reading frame of the nearly full length cDNA coded for a 369-amino acid polypeptide with a calculated Mr of 41,466. The function of this nucleotide sequence was verified by comparison with amino acid sequence of the amino terminus and tryptic peptides from purified plant enzyme, by Northern blotting with RNA from wild type and mutant plants, and by prokaryotic expression yielding an enzymatically active hydroxylase. Computer-aided sequence analysis revealed high similarity (73.5%) to flavanone 3-beta-hydroxylase from barley. Genomic Southern blot analysis showed the presence of only one gene for flavanone 3-beta-hydroxylase in P. hybrida
ISSN:0021-9258
1083-351X
DOI:10.1016/S0021-9258(18)42777-9