Cyclodextrin glycosyl transferases for producing γ-cyclodextrin
AssigneeConsortium fur Elektrochemische Industrie GmbH
InventorsGeorg E. Schulz, Goetz Parsiegla
Life of this patent
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Abstract
CGTases, which, when converting starch or starch-like substrates to CD, produce γ-CD to an increased extent and still exhibit at least 60% of the specific total CGTase activity of the starting CGTase which was used for preparing the enzyme concerned. The amino acid sequences differ from the amino acid sequences of known CGTases by the deletion of from 3 to 8 amino acids from the region from amino acid position 155 up to and including amino acid position 195, where position 1 of the protein sequence is the beginning of the signal peptide of the CGTase and the deletion brings about the increase in the γ-CGTase activity of the protein.
Claims6
A cyclodextrin glycosyltransferase (CGTase) protein which converts starch substrates to cyclodextrin (CD) produces γ-CD to an increased extent relative to the wild-type and which still exhibits at least 60% of specific total γ-CGTase activity of a starting CGTase which was used for preparing it, comprising
- an amino acid sequence which differs from the amino acid sequences of the CGTases specified in FIG. 1 by the deletion of the amino acid residues which are in each case printed in bold in FIG. 1 and is selected from the group described in Table 1 consisting of
- (SEQ ID NO:6) deleted from (SEQ ID NO:1);
- (SEQ ID NO:7;
- Glu Xaa Asn Xaa Asn) deleted from (SEQ ID NO:1);
- (SEQ ID NO:8) deleted from (SEQ ID NO:1);
- (SEQ ID NO:9) deleted from (SEQ ID NO:1);
- (SEQ ID NO:10) deleted from (SEQ ID NO:1);
- (SEQ ID NO:11) deleted from (SEQ ID NO:1);
- (SEQ ID NO:12;
- Ala Xaa Glu Xaa Asn Xaa Asn Tyr) deleted from (SEQ ID NO:
- );
- (SEQ ID No:13) deleted from (SEQ ID NO:1);
- (SEQ ID NO:14) deleted from (SEQ ID NO:2);
- (SEQ ID NO:15) deleted from (SEQ ID NO:3);
- (SEQ ID NO:16) deleted from (SEQ ID NO:4);
- (SEQ TO NO:17) deleted from (SEQ ID NO:5);
- (SEQ ID NO:11;
- Glu Xaa Asp Xaa Thr) deleted from (SEQ ID NO:5) and
- (SEQ ID NO:19) deleted from (SEQ ID NO:5),
- wherein Xaa indicates no deletion of that amino acid residue from the starting CGTase, and
- where the remaining amino acid sequence of the CGTase is homologous to the amino acid sequence of the CGTase from the microorganism which is in each case specified in FIG. 1 to the extent that the sequence exhibits CGTase activity without said deletion.
A cyclodextrin gylcosyltransferase (CGTase) protein which converts starch substrates to cyclodextrin (CD), produces γ-CD to an increased extent relative to the wild-type and which still exhibits at least 60% of specific total γ-CGTase activity of a starting CGTase which was used for preparing it, comprising
- CGTase from Bacillus sp. 1-1 having an amino acid sequence differing from the amino acid sequence of starting CGTase by deletion of between three and eight amino acids in a region from amino acid position 165 up to and including amino acid position 174 of (SEQ ID NO:21) as shown in FIG. 2;
- and
- where position 1 of protein sequence is the beginning of a signal peptide for the CGTase and deletion brings about an increase in the γ-CGTase activity of the protein.
A cyclodextrin gylcosyltransferase (CGTase) protein which converts starch substrates to cyclodextrin (CD), produces γ-CD to an increased extent relative to the wild-type and which still exhibits at least 60% of specific total γ-CGTase activity of a starting CGTase which was used for preparing it, comprising
- CGTase from Thermo anaerobacter having an amino acid sequence differing from the amino acid sequence of starting CGTase by deletion of between three and five amino acids in a region from amino acid position 171 up to and including amino acid position 180 of (SEQ ID NO:38) as shown in FIG. 3;
- and
- where position 1 of protein sequence is the beginning of a signal peptide for the CGTase and deletion brings about an increase in the γ-CGTase activity of the protein.
Dependencies are inferred from the claim text.