Modified phytases

Details Modified phytases Modified phytases

2002-02-01

2004-05-11

Saidha, Tekchand (Department: 1652)

Chemistry: molecular biology and microbiology

Enzyme , proenzyme; compositions thereof; process for...

Hydrolase

C435S252300, C435S320100, C435S913000, C435S916000, C435S917000, C536S023200

Reexamination Certificate

active

06734004

ABSTRACT:

BACKGROUND OF THE INVENTION
Phytases (myo-inositol hexakisphosphate phosphohydrolases; EC 3.1.3.8) are enzymes that hydrolyze phytate (myo-inositol hexakisphosphate) to myo-inositol and inorganic phosphate and are known to be valuable feed additives.
A phytase was first described in rice bran in 1907 [Suzuki et al., Bull. Coll. Agr. Tokio Imp. Univ. 7, 495 (1907)] and phytases from Aspergillus species in 1911 [Dox and Golden, J. Biol. Chem. 10, 183-186 (1911)]. Phytases have also been found in wheat bran, plant seeds, animal intestines and in microorganisms [Howsen and Davis, Enzyme Microb. Technol. 5, 377-382 (1983), Lambrechts et al., Biotech. Lett. 14, 61-66 (1992), Shieh and Ware, Appl. Microbiol. 16, 1348-1351 (1968)].
The cloning and expression of the phytase from
Aspergillus niger
(
ficuum
) has been described by Van Hartingsveldt et al., in Gene, 127, 87-94 (1993) and in European Patent Application, Publication No. (EP) 420 358 and from
Aspergillus niger
var. awamori by Piddington et al., in Gene 133, 55-62 (1993).
Cloning, expression and purification of phytases with improved properties have been disclosed in EP 684 313. However, since there is a still ongoing need for further improved phytases, especially with respect to the activity properties, it is an object of the present invention to provide such improvements.
SUMMARY OF THE INVENTION
Accordingly, this invention is directed to a process for the production of a modified phytase with a desired property improved over the property of the corresponding unmodified phytase which comprises:
(a) determining the three dimensional structure of the unmodified phytase and of a second phytase which has the desired property by aligning the amino acid sequences of said phytases with the amino acid sequence of a third phytase which is the phytase of
Aspergillus niger
and using the three dimensional structure of the phytase of
Aspergillus niger
as a template based on the alignment to determine said three dimensional structures;
(b) determining from the structures of step (a) the amino acids of the active sites of the unmodified phytase and of the second phytase having the desired property which active site provides the desired property and comparing the amino acids which form the active sites to identify which amino acids are different in the active site of the second phytase from the amino acids in the active site of the unmodified phytase;
(c) constructing a DNA sequence coding for the modified phytase by obtaining the DNA sequence of the unmodified phytase and changing the nucleotides coding for the active site which provides the desired property for said unmodified phytase so that at least one of the amino acids in the active site which provides the desired property is substituted by one of the amino acids which was identified as being different in step (b);
(d) integrating such a DNA sequence into a vector capable of expression in a suitable host cell; and
(e) transforming the suitable host cell by the DNA sequence of step (c) or the vector of step (d), growing said host cell under suitable growth conditions and isolating the modified phytase from the host cell or the culture medium.
Either or both of the unmodified phytase and the phytase with the desired property may be of eukaryotic origin, especially of fungal origin. Such phytases are preferably of Aspergillus origin, for example phytase from
Aspergillus fumigatus
. In a preferred process, the phytase with the desired property is a phytase from
Aspergillus terreus
. In another preferred process, the unmodified phytase is a phytase of
Aspergillus fumigatus
and the phytase with the desired property is the
Aspergillus niger
phytase. In yet another preferred process, the unmodified phytase is a phytase of
Aspergillus fumigatus
and the phytase with the desired property is the
Aspergillus terreus
phytase.
Also part of this invention is a modified phytase with a specific activity improved over the specific activity of the corresponding unmodified phytase (for example
Aspergillus fumigatus
) wherein the amino acid sequence of the corresponding unmodified phytase has been changed by one or more of deletion, substitution and addition by one or more amino acids to obtain the amino acid sequence of the modified phytase. A preferred phytase has an amino acid sequence homologous to that of the phytase of
Aspergillus niger
(SEQ ID NO:1) and has an amino acid sequence that has been changed in at least one amino acid position selected from the following amino acid positions which correspond to positions of the amino acid sequence of the phytase of
Aspergillus niger:
27, 66, 71, 103, 140, 141, 188, 205, 234, 238, 274, 277, 282, 340 and 424, in particular wherein the amino acid position is selected from 27, 66, 140, 205, 274, 277, 282, and 340.
A preferred modified phytase has an amino acid sequence which has been changed at position 27 alone or in addition to other of the above positions, in particular at least at position 66 and/or position 140. Thus preferred phytases are modified at position 27 and 66 or 27 and 140.
For any such phytase, the amino acid at position 27 may be replaced by a specific amino acid selected from one of the following groups:
a) Ala, Val, Leu, Ile; or b)Thr; or c) Asn.
Particular modified phytases of this invention are characterized by at least one of the following changes in amino acids at positions: Q27L, Q27N, Q27T, Q271, Q27V, Q27A, Q27G, S66D, S140Y, D141G, A205E, Q274L, G277D, G277K, Y282H and/or N340S.
Also part of this invention are polynucleotides comprising a DNA sequence coding for the modified phytases produced by the above method. Polynucleotides comprising DNA sequences coding for the phytases described above which are modified at particular amino acid positions are included.
Also included are vectors, especially expression vectors, which contain the polynucleotides of this invention, and host cells which contain these polynucleotides directly or within a vector.
Another aspect of this invention is a food or feed composition which contains modified phytases described above.


REFERENCES:
patent: 5436156 (1995-07-01), Van Gorcom et al.
patent: 5443979 (1995-08-01), Vanderbeke et al.
patent: 5863533 (1999-01-01), Van Gorcom et al.
patent: 6153418 (2000-11-01), Lehmann
patent: 6291221 (2001-09-01), van Loon et al.
patent: 6358722 (2002-03-01), van Loon et al.
patent: 1 492 060 (1969-03-01), None
patent: 0 035 204 (1981-09-01), None
patent: 0 299 108 (1989-01-01), None
patent: 0 420 358 (1991-04-01), None
patent: 0 422 697 (1991-04-01), None
patent: 0 619 369 (1994-10-01), None
patent: 0 684 313 (1995-11-01), None
patent: 0 747 483 (1996-12-01), None
patent: 0 758 018 (1997-02-01), None
patent: 0 897 010 (1999-02-01), None
patent: 0 897 985 (1999-02-01), None
patent: WO 91/14773 (1991-10-01), None
patent: WO 93/16175 (1993-08-01), None
patent: WO 94/03612 (1994-02-01), None
patent: WO 95/00662 (1995-01-01), None
patent: WO 98/54980 (1998-12-01), None
Dox, et al., “Phytase in Lower Fungi,”J. Biol. Chem. vol. 10, pp. 183-186 (1911).
Howson, et al., “Production of Phytase-Hydrolysing Enzyme By Some Fungi,”Enzyme Microb. Technol., vol. 5, pp. 377-382 (1983).
Lambrechts, et al., “Utilization Of Phytate By Some Yeasts,”Biotech. Lett., vol. 14, pp. 61-66 (1992).
Shieh, et al., “Survey of Microorganisms for the Production of Extracellular Phytase,”Appl. Microbiol., vol. 16, pp. 1348-1351 (1968).
Van Hartingsveldt, et al., “Cloning, Characterization and Overexpression of the Phytase-Encoding Gene (phyA) ofAspergillus niger,” Gene, vol. 127, pp. 87-94 (1993).
Piddington, et al., “The Cloning and Sequencing of the Genes Encoding Phytase (phy) and pH 2.5-Optimum Acid Phosphatase (aph) FromAspergillus nigervar.awamori,” Gene, vol. 133, pp. 55-62 (1993).
Kraulis, “MOLSCRIPT: a Program to Produce Both Detailed and Schematic Plots of Protein Structures,”J. Appl. Cryst., vol. 24, pp. 946-950 (1991).
Merritt, et al., “Raster3D Version 2.0 A Program for Photorealistic Molecular Graphics,”Acta Cryst., vol. D50, pp. 86

Affiliated with

Also associated with

Rating

Modified phytases does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Modified phytases, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Modified phytases will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-3223558