Manipulation of flavonoid biosynthesis in plants
View Patent ↗The present invention relates to nucleic acids and nucleic acid fragments encoding amino acid sequences for flavonoid biosynthetic enzymes in plants, and the use thereof for the modification of flavonoid biosynthesis in plants. More particularly, the flavonoid biosynthetic enzyme is selected from the group consisting of chalcone isomerase (CHI), chalcone synthase (CHS), chalcone reductase (CHR), dihydroflavonol 4-reductase (DFR), leucoanthocyanidin reductase (LCR), flavonoid 3′, 5′ hydrolase (F3′5′H), flavanone 3-hydroxylase (F3H), flavonoid 3′-hydroxylase (F3′H), phenylalanine ammonia-olyase (PAL) and vestitone reductase (VR), and functionally active fragments and variants thereof.
1. A substantially purified or isolated nucleic acid comprising a nucleotide sequence selected from the group consisting of:
(a) the nucleotide sequence of SEQ ID NO:305;
(b) the nucleotide sequence comprising the coding portion of SEQ ID NO: 305;
(c) the nucleotide sequence which is the full length complement of SEQ ID NO: 305; and
(d) the nucleotide sequence which is the full length complement of the coding portion of SEQ ID NO: 305.
2. A construct including the nucleic acid according to claim 1 .
3. A vector including the nucleic acid or nucleic acid according to claim 1 .
4. The vector according to claim 3 , further including a promoter and a terminator, said promoter, nucleic acid and terminator being operatively linked.
5. A plant cell, plant, plant seed or other plant part, having incorporated therein the vector according to claim 3 .
6. A plant, plant seed or other plant part derived from the plant cell or plant according to claim 5 and having incorporated therein the vector according to claim 3 .
7. A method selected from the group consisting of:
(a) modifying flavonoid biosynthesis in a plant;
(b) modifying protein binding, metal chelation, anti-oxidation, and/or UV-light absorption in a plant;
(c) modifying pigment production in plant;
(d) modifying plant defense to a biotic stress; and
(e) modifying forage quality of a plant by disrupting protein foam and/or conferring protection from rumen pasture bloat;
said method including introducing into said plant an effective amount of a nucleic acid according to claim 1 .
8. A method according to claim 7 wherein said biotic stress is selected from the group consisting of viruses, microorganisms, insects and fungal pathogens.
9. A substantially purified or isolated nucleic acid encoding BAN, said nucleic acid comprising the nucleotide sequence of SEQ ID NO: 305.
10. A substantially purified or isolated nucleic acid comprising a nucleotide sequence selected from the group consisting of:
(a) the nucleotide sequence of SEQ ID NO:305;
(b) the nucleotide sequence comprising the coding portion of SEQ ID NO: 305;
(c) the nucleotide sequence which is the full length complement of SEQ ID NO: 305;
(d) the nucleotide which is the full length complement of the coding portion of Seq ID No. 305;
(e) a nucleotide sequence which is a variant of SEQ ID NO:305 with one or more nucleotide changes that result in conservative amino acid substitutions in the encoded polypeptide with the proviso that the variant has at least approximately 98% identity to SEQ ID NO: 305; and
(f) a nucleotide sequence which is a variant of the coding portion of SEQ ID NO: 305 with one or more nucleotide changes that result in conservative amino acid substitutions in the encoded polypeptide with the proviso that the variant has at least approximately 98% identity to the coding portion of SEQ ID NO: 305.
11. A substantially purified or isolated nucleic acid encoding BAN, said nucleic acid or nucleic acid fragment comprising the nucleotide sequence that is a variant of SEQ ID NO: 305 with one or more nucleotide changes that result in conservative amino acid substitutions in the encoded polypeptide with the proviso that the variant has at least approximately 98% identity to SEQ ID No.: 305.