Method for the producing alpha-1, 6-branched alpha-1, 4-glucans from sucrose
View Patent ↗Nucleic acid molecules which encode a branching enzyme from a bacterium of the genus Neisseria , vectors, host cell, plant cells and plants containing said nucleic acid molecules as well as starch obtainable from the plants described are described. Furthermore, an in-vitro method for producing α-1,6-branched α-1,4-glucans on the basis of sucrose and a combination of enzymes of an amylosucrase and a branching enzyme as well as the α-1,6-branched α-1,4-glucans obtainable by said method are described.
1. A recombinant DNA molecule comprising a heterologous polynucleotide and a regulatory region comprising a nucleic acid selected from the group consisting of
(a) a polynucleotide comprising more than 50 nucleotides of the nucleotides 1 to 169 of the nucleotide sequence depicted in SEQ ID NO: 1 and including the nucleotide sequence 5′-TACGCGACA-3′, the nucleotide sequence 5′-ATATT-3′ and the nucleotide sequence 5′-GGGAGA-3′;
(b) a polynucleotide having the nucleotide sequence 5′-TACGCGACA-3′ spaced apart by six nucleotides from a nucleotide sequence 5′-ATATT-3′ in turn spaced apart by 101 nucleotides from a nucleotide sequence 5′-GGGAGA-3′; or
(c) a polynucleotide that hybridizes to a polynucleotide consisting of nucleotides 1469 of SEQ ID NO:1 or to the complement thereof, under conditions of 2×SSC, 0.1% SDS or 25 mM sodium phosphate buffer, 7% SDS, with washing in 0.2×SSC, 0.1% SDS and both hybridization and washing is conducted at 65-68° C. and including the nucleotide sequence 5′-TACGCGACA-3′, the nucleotide sequence 5′-ATATT-3′ and the nucleotide sequence 5′-GGGAGA-3′.
2. The recombinant DNA molecule of claim 1 , comprising the nucleotides 1 to 169 of the nucleotide sequence depicted in SEQ ID NO: 1.
3. A vector comprising:
(a) a polynucleotide comprising more than 50 nucleotides of the nucleotides 1 to 169 of the nucleotide sequence depicted in SEQ ID NO: 1 and including the nucleotide sequence 5′-TACGCGACA-3′, the nucleotide sequence 5′-ATATT-3′ and the nucleotide sequence 5′-GGGAGA-3′;
(b) a polynucleotide having the nucleotide sequence 5′-TACGCGACA-3′ spaced apart by six nucleotides from a nucleotide sequence 5′-ATATT-3′ in turn spaced apart by 101 nucleotides from a nucleotide sequence 5′-GGGAGA-3′; or
(c) a polynucleotide that hybridizes to a polynucleotide consisting of nucleotides 1-169 of SEQ ID NO:1 or to the complement thereof, under conditions of 2×SSC, 0.1% SDS or 25 mM sodium phosphate buffer, 7% SDS, with washing in 0.2×SSC, 0.1% SDS and both hybridization and washing is conducted at 65-68° C. and including the nucleotide sequence 5′-TACGCGACA-3′, the nucleotide sequence 5′-ATATT-3′ and the nucleotide sequence 5′-GGGAGA-3′.
4. The vector of claim 3 , comprising the nucleotides 1 to 169 of the nucleotide sequence depicted in SEQ ID NO: 1.
5. A recombinant DNA molecule comprising a heterologous polynucleotide and a regulatory region comprising a nucleic acid obtained by amplification of a template genomic DNA of a Neisseria species using a primer comprising nucleotides 1-15 of SEQ ID NO: 1 and a primer comprising the complement of nucleotides 154-169 of SEQ ID NO: 1.
6. The recombinant DNA molecule of claim 5 , in which the regulatory region includes the nucleotide sequence 5′-TACGCGACA-3′, the nucleotide sequence 5′-ATATT-3′ and the nucleotide sequence 5′-GGGAGA-3′.
7. A vector comprising a regulatory region comprising a nucleic acid obtained by amplification of a template genomic DNA of a Neisseria species using a primer comprising nucleotides 1-15 of SEQ ID NO: 1 and a primer comprising the complement of nucleotides 154-169 of SEQ ID NO: 1.
8. The vector of claim 7 , in which the regulatory region includes the nucleotide sequence 5′-TACGCGACA-3′, the nucleotide sequence 5′-ATATT-3′ and the nucleotide sequence 5-GGGAGA-3′.