Mutant EGIII cellulase, DNA encoding such EGIII compositions...

Details Mutant EGIII cellulase, DNA encoding such EGIII compositions... Mutant EGIII cellulase, DNA encoding such EGIII compositions...

2000-08-04

2003-10-21

Patterson, Jr., Charles L. (Department: 1652)

Chemistry: molecular biology and microbiology

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

Hydrolase

C510S392000, C241S028000, C426S656000

Reexamination Certificate

active

06635465

ABSTRACT:

BACKGROUND OF THE INVENTION
Cellulases are enzymes that are capable of hydrolysis of the &bgr;-D-glucosidic linkages in celluloses. Cellulolytic enzymes have been traditionally divided into three major classes: endoglucanases, exoglucanases or cellobiohydrolases and &bgr;-glucosidases (Knowles, J. et al., (1987),
TIBTECH
5, 255-261); and are known to be produced by a large number of bacteria, yeasts and fingi.
Although cellulases are used to degrade wood pulp and animal feed, cellulases are primarily used in the treatment of textiles, e.g., in detergent compositions for assisting in the removal of dirt or grayish cast (see e.g., Great Britain Application Nos. 2,075,028, 2,095,275 and 2,094,826) or in the treatment of textiles prior to sale to improve the feel and appearance of the textile. Thus, Great Britain Application No. 1,358,599 illustrates the use of cellulase in detergents to reduce the harshness of cotton containing fabrics.
Cellulases have also been used in the treatment of textiles to recondition used fabrics by making their colors more vibrant (see e.g.,
The Shizuoka Prefectural Hammamatsu Textile Industrial Research Institute Report
24:54-61 (1986)). Repeated washing of cotton containing fabrics results in a grayish cast to the fabric which is believed to be due to disrupted and disordered fibrils, sometimes called “pills”, caused by mechanical action. This greyish cast is particularly noticeable on colored fabrics. As a consequence, the ability of cellulase to remove the disordered top layer of the fiber and thus improve the overall appearance of the fabric has been of value.
Because of its effectiveness in many industrial processes, there has been a trend in the field to search for specific cellulase compositions or components that have particularly effective performance profiles with respect to one or more specific applications. As possible sources of cellulases, practitioners have focused on fuigi and bacteria. For example, cellulase produced by certain fungi such as Trichoderma spp. (especially
Trichoderma reesei
) have been given much attention because a complete cellulase system capable of degrading crystalline forms of cellulose is readily produced in large quantities via fermentation procedures. This specific cellulase complex has been extensively analyzed to determine the nature of its specific components and the ability of those components to perform in industrial processes (see, Wood et al., “Methods in Enzymology”, 160, 25, pages 234, et seq. (1988). U.S. Pat. No. 5,475,101 (Ward et al.) discloses the purification and molecular cloning of one particularly useful enzyme called endoglucanase III (EGIII) which is derived from
Trichoderma reesei.
PCT Publication No. WO 94/14953 discloses endoglucanases that are encoded by a nucleic acid which comprises any one of a series of DNA sequences, each having 20 nucleotides.
Ooi, et al.,
Curr. Genet
. 18:217-222 (1990) disclose the cDNA sequence coding for endoglucanase F1-CMC produced by
Aspergillus aculeatus
that contains the amino acid strings NNLWG, ELMIW and GTEPFT. Sakamoto, et al.,
Curr. Genet
. 27:435-439 (1995) discloses the cDNA sequence encoding the endoglucanase CMCase-1 From
Aspergillus kawachii
IFO 4308 which contains the amino acid strings ELMIW and GTEPFT. Ward, et al., discloses the sequence of EGIII having the amino acid strings NNLWG, ELMIW and GTEPFT. Additionally, two cellulase sequences, one from
Erwinia carotovara
and
Rhodothermus marinus
are disclosed in Saarilahti, et al., Gene 90:9-14 (1990) and Hreggvidsson, et al.,
Appl. Environ. Microb
. 62:3047-3049 (1996) that contain the amino acid string ELMIW.
Despite knowledge in the art related to many cellulase compositions having applications in some or all of the above areas, there is a continued need for new cellulase compositions which have improved stability under conditions present in applications for which cellulases are useful, e.g., household and laundry detergents and textile treatment compositions.
SUMMARY OF THE INVENTION
A variant EGIII cellulase is provided, wherein the cellulase comprises a substitution at a residue that is sensitive to temperature stress and wherein the variant EGIII cellulase is derived from
T. reesei
EGIII cellulase. In a preferred embodiment, the variant comprises a substitution or deletion at a position corresponding to one or more residues W7, G31, A35, H45, S63, S77, M79, H108, T145, Y147, M154, Q162, T163, N167, N174, and/or V192 in EGIII. In a more preferred embodiment, the variant comprises a substitution at a position corresponding to one or more of residues W7Y, G31Q, A35V, H45Q, S63V, S77G, M79I, H108R, T145E, Y147W, M154N, Q162P, T163S, N167S, N174D and/or V192L.
In an alternative embodiment of this invention, a DNA that encodes a variant EGIII cellulase is provided. In a preferred embodiment, the DNA is in a vector. In another aspect of this embodiment the vector is used to transfect a host cell.
In yet another embodiment, a method of producing a variant EGIII cellulase having improved stability and/or performance is provided. The method comprises the steps of culturing the host cell in a suitable culture medium under suitable conditions to produce cellulase and obtaining said produced cellulase. In still another embodiment, a detergent composition comprising a surfactant and a variant EGIII cellulase is provided, wherein the cellulase comprises a variant EGIII cellulase comprising a substitution at residue sensitive to temperature. In a preferred embodiment, the variant EGIII cellulase comprises a substitution or deletion at a position corresponding to one or more residues W7, G31, A35, H45, S63, S77, M79, H108, T145, Y147, M154, Q162, T163, N167, N174, and/or V192in EGIII. In a most preferred embodiment, the variant EGIII cellulase comprises a substitution at a position corresponding to one or more of residues at position W7Y, G31Q, A35V, H45Q, S63V, S77G, M79I, H108R, T145E, Y147W, M154N, Q162P, T163S, N167S, N174D and/or V192L.
In another embodiment the variant EGIII cellulase of this invention is used in the treatment of a cellulose-containing textile, in particular in ston washing indigo dyed denim. In other aspects of this embodiment, the cellulase of this invention is used as a feed additive, in the treatment of wood pulp, and in the reduction of biomass to glucose.


REFERENCES:
patent: 4760025 (1988-07-01), Estell et al.
patent: 4832864 (1989-05-01), Olson
patent: 5185258 (1993-02-01), Caldwell et al.
patent: 5246853 (1993-09-01), Clarkson et al.
patent: 5254283 (1993-10-01), Arnold et al.
patent: 5290474 (1994-03-01), Clarkson et al.
patent: 5475101 (1995-12-01), Ward et al.
patent: 6187577 (2001-02-01), Jones et al.
patent: 6268328 (2001-07-01), Mitchinson et al.
patent: 220 016 (1991-08-01), None
patent: 271 004 (1993-04-01), None
patent: 1358599 (1974-07-01), None
patent: 2075028 (1981-11-01), None
patent: 2 094 826 (1982-09-01), None
patent: 2095275 (1982-09-01), None
patent: WO 92/06209 (1992-04-01), None
patent: WO 94/14953 (1994-07-01), None
patent: WO 94/28117 (1994-12-01), None
patent: WO 98/31821 (1998-07-01), None
patent: WO 99/31255 (1999-06-01), None
patent: WO 00/09707 (2000-02-01), None
patent: WO 00/14206 (2000-03-01), None
patent: WO 00/14208 (2000-03-01), None
patent: WO 00/37614 (2000-06-01), None
patent: WO 01/47956 (2001-07-01), None
patent: WO 02/12464 (2002-02-01), None
patent: WO 02/12465 (2002-02-01), None
patent: WO 02/12466 (2002-02-01), None
Accession No. Q12679, 1997.*
Accession No. S12610, 1994.*
.Accession No. 013454, 1998.*
Accession No. P22669, 1991.*
Altschul, S. et al., “Basic Local Alignment Search Tool,”J. Mol. Biol.,Vol 215, No. 3, pp. 403-410, 1990.
Ausubel, Frederick et al.,Short Protocols in Molecular Biology, Current Protocols in Molecular Biology,2nded., Greene Publishing Associates & John Wiley & Sons. New York, N.Y. 1992, 12-24 to 2-38.
Bergés, T. et al., “Isolation of uridine auxotrophs fromTrichoderma reeseiand efficient transformation with the cloned ura3 and ura5 genes,”Curr. Genet.vol. 19, No. 5, pp. 359-365, 1991.
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