The present invention relates to a cellulase capable of re¬ moving soil from fabric, a detergent composition comprising the cellulase, a method of treating soiled fabric with the cellulolytic enzyme, and use of the cellulase e.g. in deter¬ gent compositions, in fabric softerners, for colour clarifi¬ cation of textile fabrics (removal of fluffs and pills) , for preventing backstaining in washing of fabric, for soil remo¬ val, for deinking of used paper, and for pulp recycling.

BACKGROUND OF THE INVENTION

Repeated washing of fabrics, especially cellulose containing fabrics, generally causes a harshness in the fabric used. The use of cellulases, i.e. cellulolytic enzymes, for harsh¬ ness reduction of cellulose containing fabrics, e.g. cotton, was suggested and demonstrated a long time ago.

The practical exploitation of cellulases has, to some ex¬ tent, been set back by the nature of the known cellulase preparations which are often complex mixtures of a variety of single cellulase components, and which may have a rather low specific activity. It is difficult to optimise the pro- duction of single components in multiple enzyme systems and thus to implement industrial cost-effective production of cellulases, and their actual use has been hampered by dif¬ ficulties arising from the need to employ rather large quan¬ tities of the enzymes to achieve the desired effect.

The drawbacks of previously suggested cellulases may be re¬ medied by using single-component enzymes selected for a high specific activity. Single-component cellulases are described in, e.g. WO 91/17243, WO 91/17244 and WO 91/10732.

E.g. in WO 91/17244 is disclosed a cellulose-degrading en¬ zyme (a cellulase) derivable from a fungus other than Tri- choderma or Phanerochaete which comprises a carbohydrate binding domain homologous to a terminal A region of Tricho- derma reeεei cellulases, the carbohydrate binding domain being capable of effecting binding of the enzyme to an inso¬ luble cellulosic substrate, which may be employed for tex¬ tile treatment, e.g. for reducing the harshness of cotton- containing fabrics and for soil removal and colour clarifi- cation of fabrics. In example 3 and fig. 13 is disclosed the preparation of a Fusarium oxysporum C-family endoglucanase and the DNA sequence and derived amino acid sequence there¬ of, respectively. Later it was found that the disclosed amino acid sequence was not correct; the corrected sequence is published in Sheppard, P.O., Grant, F.J., Oort, P.J., Spreσher, CA. , Foster, D.C., Hagen, F.S., Upshall, A., Mcknight, G.L. and Ohara, P.J. : The use of conserved cellu¬ lase family-specific sequences to clone cellulase homolog cdnas from fusarium-oxysporum. Gene . 150:163-167, 1994. In example 4 and Fig. 14A-E is disclosed the preparation of a Humicola insolens endoglucanase 1 (EG I) and the DNA sequ¬ ence and derived amino acid sequence thereof, respectively. Further, in example 4 (page 32, line 1 to 5) is described the construction of expression plasmid of a truncated EG I (denoted EG I') wherein the last 13 amino acids of the co¬ ding region were eliminated and the altering of Val to Leu in position 421 (position 401 in the sequence of the enzy¬ me) . The gist of the invention disclosed in WO 91/17244 is to provide a cellulase which, besides the enzyme core, has a carbohydrate binding domain (CBD) which is homologous to the A region of Trichoderma reeεei cellulases, since the func¬ tion of the CBD in the enzyme molecule was believed to be to mediate binding to solid substrates including cellulose and consequently to enhance the activity of such enzymes towards such substrates.

The problem underlying the present invention is to obtain single-component endoglucanases having enhanced enzyme ac¬ tivity in the alkaline pH range, while at the same time exerting a moderate cellulolytic action on the cellulosic substrate. In other words, the endoglucanase should neither destroy the cellulosic substrate as such. For example, when the substrate is a cellulosic fabric, the used endoglucanase should not result in a substantial tensile strength loss of the fabric. The enhanced alkaline activity of the enzyme is also essential, since most applications of endoglucanases advantageously take place in the alkaline pH range.

SUMMARY OF THE INVENTION

Surprisingly, it has now been found that certain cellulases which do not comprise a carbohydrate binding domain, i.e. essentially consist of the core enzyme, or which at least do not comprise a carbohydrate binding domain which is homolo- gous to the A region of Trichoderma reeεei cellulases, may have an enhanced activity. This may for example result in improved soil removal from fabrics.

Preferably, the cellulases of the invention are endoglucana- ses which have the amino acid residue tryptophan (Trp or W) in the position corresponding to position 55 of the struc- turral homology frame in Figure 5.

More specifically, it has been found that cellulases selec- ted from the group consisting of cellulases classified in family 7 as described in Henrissat, B. et al.: Biochem. J. (1993), 293. p. 781-788, and cellulase variants derived from a parent cellulase classified in family C, comprising a core and optionally a C-terminal link consisting of 10 amino acids at the most may perform excellent in detergents with respect to soil removal in comparison with the known cellu¬ lases.

In one aspect, the invention relates to endoglucanases which may be truncated, e.g. genetically truncated, variants of known endoglucanases, and the use thereof e.g. for washing, cleaning, deinking'and pulping purposes.

In another aspect, the invention relates to cellulases ha¬ ving high activity on cellotriose in the presence of a de¬ tergent matrix, high dispersing action on carbon black, and high alkaline activity on acid swollen cellulose at pH 8.

The present endoglucanases are useful e.g. for soil removal and may thus be applied to detergent compositions, detergent additives and/or fabric softeners.

Other uses of the present endoglucanases are for colour clarification of textile fabrics (removal of fluffs and pills) , for preventing backstaining in washing of fabric, for soil removal, for deinking of used paper, and for pulp recycling.

DETAILED DESCRIPTION OF THE INVENTION

In the present specification and claims, the term "cellul- ase" denotes an enzyme that hydrolyses cellulose. The cel¬ lulase may be a component occurring in a cellulase system produced by a given microorganism, such a cellulase system mostly comprising several different cellulase enzyme compo¬ nents including those usually identified as e.g. cellobiohy- drolases, exo-cellobiohydrolases, endoglucanases, β-glucosi- dases. Alternatively, the cellulase may be a single compo¬ nent, i.e. a component essentially free of other cellulase components usually occurring in a cellulase system produced by a given microorganism, the single component being a re- combinant component, i.e. produced by cloning of a DNA sequ¬ ence encoding the single component and subsequent cell transformed with the DNA sequence and expressed in a host.

The host is preferably a heterologous host, but the host may under certain conditions also be the homologous host.

In a preferred embodiment of the invention, the cellulase is an endoglucanase.

The term "soil removal" or "particulate soil removal", as used herein, refers to enhanced cleaning of cellulose-con¬ taining fabrics or garment, e.g. cotton, contaminated by particles of soil or of other insoluble matter entrapped by microfibrills spreading out on the fibre surface.

In the present context, the term "homologous" or "homologous sequence" is intended to indicate an amino acid sequence differing from those of Figure 1, 2, 3, 4, 5 and 6, respec¬ tively, by one or more amino acid residues. The homologous sequence may be one resulting from modification of an amino acid sequence shown in these figures, e.g. involving substi¬ tution of one or more amino acid residues at one or more different sites in the amino acid sequence, deletion of one or more amino acid residues at either or both ends of the enzyme or at one or more sites in the amino acid sequence, or insertion of one or more amino acid residues at one or more sites in the amino acid sequence. The modification of the amino acid sequence may suitably be performed by modi¬ fying the DNA sequence encoding the enzyme, e.g. by site- directed or by random mutagenesis or a combination of these techniques in accordance with well-known procedures. Alter¬ natively, the homologous sequence may be one of an enzyme derived from another origin than the cellulases correspon¬ ding to the amino acid sequences shown in Figure 1, 2, 3, 4, 5, and 6, respectively. Thus, "homologue" may e.g. indicate a polypeptide encoded by DNA which hybridizes to the same probe as the DNA coding for the cellulase with the amino acid sequence in question under certain specified conditions (such as presoaking in 5xSSC and prehybridising for 1 h at -40°C in a solution of 20% formamide, 5xDenhard't's solu-

tion, 50 mM sodium phosphate, pH 6.8, and 50 μg of denatured sonicated calf thymus DNA, followed by hybridization in the same solution supplemented with 100 μM ATP for 18 h at -40°C) . The homologous sequence will normally exhibit a deg- ree of homology (in terms of identity) of at least 50%, such as at least 60%, 65%, 70%, 75%, 80%, 85%, 90% or even 95% with the amino acid sequences shown in Figure 1, 2, 3, 4, 5 and 6, respectively.

Preferably, the degree of homology is based on three-dimen¬ sional structural homology of the cellulases. For example, the Applicant has prepared the sequence alignment shown in Figure 5, wherein the amino acid sequences of three endoglu¬ canases and one cellobiohydrolase were aligned:

EGl-F: Fuεarium oxyεporum endoglucanase EG1

(fus_egl_nat.pdb, a-chain) EGl-H: Humicola inεolenε endoglucanase EG1 (legi.pdb, a-chain) EG1-T: Trichoderma reeεei endoglucanase EG1 (no pdb structure) CBHl: Trichoderma reeεei cellobiohydrolase (lcel.pdb, a-chain)

The references in the brackets refer to the Brookhaven Data¬ base identification for entries.

Initially the sequences were aligned based on secondary structure homology, but superimposition and visual examina- tion 'of the X-ray structures of EGl-F, EGl-H and CBHl neces¬ sitated several modifications of the sequence alignment. The final output in Fig. 5 is based on three-dimensional structural alignment.

The C-terminals are visible to different extents in the three crystal structures. Following the common sequence motif IGST (Res#445-449) , three residues are visible in EG1-

F, one in EGl-H, and five in CBHl. For the sequence com¬ parison in Table 1 below, residues from the N-terminals to the C-terminal motif NPSG in CBHl are included (Res#453 in Fig. 5), i.e. 402 residues from EGl-F and EGl-H, 373 residu- es from EG1-T and 434 residues from CBHl.

Table 1. Sequence identities calculated relative to the lengths of each one of the sequences (seql & seq2) : seql\seq2 EGl-H EG1-T CBHl EGl-F 58% & 58% 41% & 44% 41% & 38% EGl-H ********* 41% & 44% 4 ₀ % _{& 3} 7% EG1-T ********* ********* 47% _$ 40%

In Table 2 below is listed the disulfide bridges found in EGl-F, EGl-H and CBHl. Based on structural homology the equivalent positions for EG1-T are indicated.

Table 2. Disulfide bridges in EGl-F, EGl-H and CBHl. Based on the sequence alignment in Fig. 1, the equivalent posi- tions are indicated for EG1-T. The numbers refer to those in Fig. 5.

EGl-H and EGl-F contain the same 9 disulfide bridges.

The deletion around Res#260 in EGl-T prevents the formation of two disulfide bridges: C215-C234 & C239-C315 (EGl-H nu - bering) . It is possible that the EGl-T structure has moved relative to EGl-H and EGl-F to enable the formation of a disulfide bridge between C215 and C315 (C212 & C291 in EGl-T numbering) . The remaining 7 disulfide bridges found in EG1- F and EGl-H are also present in EGl-T.

CBHl contains the same 9 disulfide bridges as EGl-F and EG1- H, and one additional disulfide bridge in the N-terminal region.

CBHl contains the most insertions relative to the others, and these insertions are predominantly located at the edges of the substrate binding cleft, possibly contributing to the fact that CBHl is a cellobiohydrolase.

When attempting to explain the improved alkaline activity of EGl-H and EGl-F relative to EGl-T, the following loops may be the most interesting, as they contain charges in the pro¬ ximity of the active site. Charges can alter the pKa values of the catalytic residues, and interact with the transfer of electrons during catalysis.

a) the 11-residue insertions (relative to EGl-T) at pos. 229 in EGl-H and EGl-F (Res#254) are located above the active site residues (E197, D199 & E202) and contain 2 or 3 charged residues.

b) the 5-residue insertions (relative to EGl-T) at pos. 320 in EGl-H and EGl-F (Res#355) are located at the end of the substrate binding pocket and contain 2 or 3 charged residues.

c) the 2-residue insertions (relative to EGl-T) at pos. 259 in EGl-H and EGl-F (Res#291) are located close to the b) insertion above, and contain a charged lysine residue.

The amino acid compositions of the four enzymes, i.e. EGl-F, EGl-H, EGl-T and CBHl) including the residues used in the sequence identity Table 1 above (i.e. including Res#453) , are shown in Table 3.

Table 3. Amino acid compositions 6 pKa values used for pi calculation

The isoelectric points (pi) were estimated for each of the four cellulases (shown in Table 4 below) , employing standard pKa values. It was assumed that the N-terminals are blocked, that no free C-terminal is present in the core enzymes, and that no metal ions are bound. The calculations do not con¬ sider the effects of deaminations.

Table 4. Isoelectric point

The difference between the calculated and actual pi values may be due to deaminating, e.g. Asn to Asp, which lower the actual pi.

From the amino acid compositions and the pKa values it is possible to calculate at different pH values the (partial) charges on all titrable amino acids. In this way the net charges and the sum of positive and negative charges were calculated at pH 4, 6, 8 and 10, as shown in Table 5.

The two alkaline cellulases, EGl-H and EGl-F, share the com¬ mon characteristic, that over a broad pH-interval (pH 4-10)

they contain at least 70 charged residues. The acidic EGl-T in contrast contains fewer than 50 charged residues within this pH-interval. The more densely charged surfaces of EG1- F and EGl-H may be responsible for the improved performance in laundry detergents relative to EGl-T.

Table 5. Charges as a function of pH. The first number is the net charge (e.g. (+13)+(-17)=-4) , the second is the total number of charges (e.g. J +13 j +j -17 !=+30) .

To examine the active site region in more detail, amino acids located within 10 A of the active site residues E197, D199 and E202 were identified for EGl-H and EGl-F. The fol- lowing residues belong to this 10 A subset in EGl-H (EGl-H numbering) :

108,124,129,131,133,135,138-139,141-151,171-177,193-220,2 33- 243,245,252,266,268,270,272,280,283,285,287,310,323,326,328, 331-336,338-347,354,356-358,362,384,386.

The 10 A subset in EGl-F contain essentially the same resi¬ dues as EGl-H 10 A subset. EGl-T differs more significant¬ ly, in particular with respect to the segments around 219- 221 and 230-240 in EGl-H and EGl-F, which are absent in EG1- T. Approx. 80 % sequence identity exists between EGl-F and EGl-H within the 10 A subset, whereas the residues in the equivalent 10 A subset for EGl-t are more different. Of particular interest are differences involving charges.

Within the 10 A subset a number of mutations in EGl-H & EG1- F, aiming at affecting catalysis by changing electrostatics, are contemplated based on sequence homology to EGl-T. To decrease pi within' this region M142E, K217A, K218T (in EGl-H only) and R245G is contemplated, and to increase pi E150Q, I310D, E334K (in EGl-H) and D334K (in EGl-F) are contempla¬ ted.

The following amino acid residues are in close contact with cellobiose (bound to the EGl-F) ; the numbering refers to the EGl-F numbering:

Hydrogen bonding between enzyme and inhibitor: a) R106 conserved in all 4 cellulases b) Y145 conserved in all 4 cellulases c) S345 conserved in all 4 cellulases

Within 5 A of cellubiose (excluding three active site residues, and the three H-bonding residues above): d) D34 conserved in all 4 cellulases e) W51 also W51 in EGl-H. This W appears to be important for binding of the second sugar moiety in cellubiose (relati¬ ve to the active site) . f) S104 conserved in all EGls g) A143 also A143 in EGl-H h) Y171 conserved in all 4 cellulases i) D173 conserved in all 4 cellulases j) Q175 conserved in all 4 cellulases k) Y177 not conserved

1) W347 conserved in all 4 cellulases. This W347 appears to be important for binding of the first sugar moiety in cel¬ lobiose (relative to the active site) .

Most of these residues are highly conserved. This implies that mutating them may be not of any advantage, but it cer-

tainly does not mean that the performance of EGls cannot be improved by replacement of these residues. They are all located in the active site region, and in fact this makes them very interesting, as property changes are likely to be more significant. Therefore, it is contemplated that substi¬ tutions at all these positions are preferred substitutions.

The advantage of EGl-H is its ability to induce soil removal with minimal fabric damage. What is characteristic about EGl-H and EGl-F compared to Carezyme (4egv.pdb) and Ther o- monospora fusca EG1 is a comparatively deep substrate bin¬ ding cleft, possibly preventing the access of intact cotton fibers into the catalytic site.

In EGl-F and EGl-H the substrate binding cleft is 18-20 A deep when measuring the distances between the Cα atoms of the active site residues (E197, D199 & E202) and the Cα atoms of the residues located at the upper rim of the sub¬ strate binding pocket (G351 & A229 in EGl-H) . The pocket is approx 19 A wide, when measuring between Cα atoms of the two rim residues.

In contrast, the depth of the substrate binding pocket in Carezyme ^* (4egv.pdb) , when measured in a similar manner, is only 8-10 A, whereas the width at the rim is approx. 9 A.

In T. fuεca EG1 (ltml.pdb) the depth of the pocket is ap¬ prox. 10 A, and the width approx. 18 A.

The present invention relates to a cellulase which is selec¬ ted from the group consisting of cellulases classified in family 7 as described in Henrissat, B. et al. : Biochem. J. (1993), 293. p. 781-788, and cellulase variants derived from a parent cellulase classified in family C, wherein the cel- lulase comprises a core and optionally a C-terminal link consisting of 10 amino acids at the most, provided that the

cellulase is different from the endoglucanase having the amino acid sequence listed in Figure 1.

The classification by Henrissat is a new classification sy- stem for glycosyl hydrolases based on sequence comparisons and hydrophobic cluster analyses which have shown that the catalytic domains of glycosyl hydrolases fall into 45 dis¬ tinct families, of which 11 (originally denoted A-K) contain enzymes with cellulolytic activity.

Thus far, structures of the catalytic domains of cellulases from four families have been published:

Cellobiohydrolase II (CBH II) from Trichoderma reesei (Rou- vinen et al. 1990) and endocellulase E2 from Thermomonospora fusca (Sapezio et al. 1993) from family 6(B),

Cellobiohydrolase I (CBH I) from T. reesei (Divne et al. 1994) from family 7 (C) ,

CelA from Clostridium thermocellum (Juy et al. 1992) from family 9(E); and the endoglcucanase V from H. insolens (Da- vies et al. 1993) from family 45(K).

The cellulases of the invention may be obtainable by or der¬ ived from a strain of Humicola, Trichoderma, Myceliophthora, Penicillium, Irpex, Aεpergilluε, Scytalidium or Fuεarium , preferably from a strain of Humicola, Trichoderma, Myceli¬ ophthora, Scytalidium or Fuεarium , more preferably from a strain of Humicola inεolenε, Fusarium oxyεporum , Mycelioph¬ thora thermophila or Trichoderma reeεei .

The cellulase of the invention can advantageously have one or more insertions of between 1 and 25, preferably between 1 and 20, amino acid residues; preferably the insertion is re¬ lative to EGl-Tat position 230-240 in EGl-H and EGl-F and part of which is located within loA of the active site resi- dues E197, D199 and E202.

In another aspect, the cellulase of the invention has a sub¬ strate binding cleft with a depth of at least 12A, pre¬ ferably lδA, when measuring between Cα atoms of the active site residues located at the bottom of the cleft and Cα atoms of residues located at the rim of the substrate bin¬ ding cleft immediately above the active site residues.

According to the invention, cellulases which essentially consists of the core and optionally a C-terminal link having 10 amino acids at the most may perform excellent for parti- culate soil removal when used for washing/laundry or fabric softening purposes. In Figure 1 is disclosed the amino acid sequence of a genetically truncated endoglucanase from Humi¬ cola inεolenε of 402 amino acid residues which is disclosed in WO 91/17244 as mentioned above (denoted EG I'). In Figure 3 is disclosed the amino acid sequence of a genetically truncated endoglucanase from Humicola inεolenε of 402 amino acid residues, this particular endoglucanase hereinafter being denoted EG I*. In Figure 4 is disclosed the amino acid sequence of a genetically truncated endoglucanase from Fuεa¬ rium oxyεporum , this particular endoglucanase hereinafter being denoted EGI-Fus. In figure 6 is disclose the amino acid sequence of an endoglucanase from Myceliophthora ther- mophila . Without being bound to the theory it is believed that an enhanced enzyme activity may be obtained by provi¬ ding cellulases, especially endoglucanases, which essenti¬ ally consists of a core. The cellulase may further comprise a C-terminal link, a "tail", which is relatively short, the short C-terminal link not contributing negatively to the enzyme activity. Thus it is believed that cellulases of the invention may be derived from known cellulases e.g. by "truncating" the C-terminal wholly or partly from the enzyme protein in question. The mentioned EG I* is thus derived from the known endoglucanase EG I (see WO 91/17244, Fig.l4A- E) by eliminating the last 13 amino acids of the coding re¬ gion. Furthermore, the amino acid residues in the positions 162, 203, 211 and 401, respectively, are substituted (162:

Ser to Pro; 203: Val to Ala; 211: Val to Ala; 401: Val to Leu) .

It is contemplated that cellulases which have an amino acid sequence being at least 60% homologous with the amino acid sequences listed in Figure 1, 3 and 4, respectively, also have enhanced activity resulting in improved soil removal from fabrics.

In Figure 2 is listed an alignment of the amino acid sequen¬ ce of three known endoglucanases from Humicola inεolenε (de¬ noted EGIHUM and having 415 amino acids) , -Fusarium oxyεporum (denoted Cendofus and having 409 amino acids) and Trichoder¬ ma reeεei (denoted Egltrite and having 435 amino acids) , re- spectively.

Accordingly, the invention further relates to a cellulase which is derivable from a strain of Humicola inεolenε and comprises the amino acid residues 1-397 listed in Figure 3 and optionally a C-terminal link consisting of 10 amino acids at the most, or a variant of said cellulase having an amino acid sequence being at least 60% homologous with said sequence; a cellulase which is derivable from a strain of Fuεarium oxyεporum and comprises the amino acid residues 1- 401 listed in Figure 4 and optionally a C-terminal link con¬ sisting of 10 amino acids at the most, or a variant of said cellulase having an amino acid sequence being at least 60% homologous with said sequence; a cellulase which is deri¬ vable from a strain of Trichoderma reeεei and comprises the amino acid residues 1-369 listed in Figure 2 (the amino acid sequence denoted Egltrire) and optionally a C-terminal link consisting of 10 amino acids at the most, or a variant of said cellulase having an amino acid sequence being at least 60% homologous with said sequence; and cellulase according to claim 4, which is derivable from a strain of Mycelioph- thora thermophila and comprises the amino acid residues 1- 456, preferably the residues 1-420, more preferably the re-

sidues 21-420, listed in Figure 6 and optionally a C-termi¬ nal link consisting of 10 amino acids at the most, or a var¬ iant of said cellulase having an amino acid sequence being at least 60% homologous with said sequence, provided that the cellulase is different from the endoglucanase having the amino acid sequence listed in Figure 1. The pi of the cellu¬ lase from Myceliophthora thermophila was found to be 4.0.

Examples of variants of these cellulases are variants wherein one or more of the following amino acid residues are substituted: N89Q, N89Q+N247Q, H123N, T385N, Q399N, E202A, S37W+P39W.

Other useful variants are those wherein one or more of the following amino acid residues are substituted: M142E, K217A, K217A+K218T, R245G, I310D, E150Q, E334K, M198L.

Yet other useful cellulase variant are those wherein one or more of the following amino acid residues within 5A of bound cellobiose are substituted:

R106X, Y145X, S345X, D34x, W51x, S104X, A143X, Y171X, D173X, Q175x, Y177x, W347x, where x is chosen to modify H-bonding potential and/or hydrophobic interaction with the substrate.

The activity of the present cellulases with respect to soil removal may be correlated to specific analytical methods.

Accordingly, the present invention further relates to a cel- lulase having high activity on cellotriose in the presence of a detergent matrix, high dispersing action on carbon black, and high alkaline activity on acid swollen cellulose at pH 8.

More specifically, the activity on cellotriose (see below) in the presence of a detergent matrix corresponds to an ap¬ parent k _clrt at pH 8 of preferably at least 1 per sec; the

dispersing action on carbon black at pH 10 corresponds to a delta value preferably of at least 0.20 measured at 582 nm for 5 mg/1 of cellulase (see e.g. example 2) ; and the alka¬ line activity on acid swollen cellulose at pH 8 corresponds to an apparent k _cst preferably of at least 10 per sec (see below) .

EG I* (from Humicola inεolenε ] see Fig. 3) has an apparent molecular weight (MW) of about 50kD due to glycosylation of the molecule. It is believed that the "true" MW is about

46kD. The pi of EG I* is at least about 0.4 lower than of EG I, since pi of EG I* is about 5.1-5.3 whereas pi of EG I is about 5.5-6.2.

EGI-Fus (from Fuεarium oxyεporum; see Fig. 4) has a apparent molecular weight (MW) of 48 kD; the amino acid composition gives 45 kD with 2 N glycosylation sites. The actual pi is above 9, and the theoretical pi is 9 which has been cal¬ culated based on the amino acid composition and using the pKa values from C. Tanford in Adv. Protein Chem. vol 17 pages 69-165, 1962. The molar extinction coefficient (based on the amino acid composition) has been calculated to 58180. It has been found that the stability of EGI-Fus is optimal at 50 degrees Celsius. The enzyme exhibits no activity above 60 degrees Celsius. The catalytic activity on cellotriose at pH 8,5 and 40°C has been calculated to 5,5 K _cat per sec. Km is 0,5 mM. Further, the activity on CMC is about 315 ECU per mg protein. The activity of EGI-Fus can be inactivated by 3- epoxybutyl cellobioside; see e.g. G. Legler and E. Bause, Carbohydrate Research vol 28 (1973) page 45-52: Epoxyalkyl oligo (1-4) beta-D-Glucosides as active site directed inhi¬ bitors of cellulases.

The cellulases of the invention may be obtained from the mi- croorganism in question by use of any suitable technique. For instance, a cellulase preparation may be obtained by fermentation of a microorganism and subsequent isolation of

a cellulase containing preparation from the fermented broth or microorganism by methods known in the art, but more pre¬ ferably by use of recombinant DNA techniques as known in the art. Such method normally comprises cultivation of a host cell transformed with a recombinant DNA vector capable of expressing and carrying a DNA sequence encoding the cel¬ lulase component in question, in a culture medium under con¬ ditions permitting the expression of the enzyme and recover¬ ing the enzyme from the culture.

Cloning a DNA sequence encoding a cellulase

The DNA sequence encoding a parent cellulase may be isolated from any cell or microorganism producing the cellulase in question by various methods, well known in the art. First a genomic DNA and/or cDNA library should be constructed using chromosomal DNA or messenger RNA from the organism that pro¬ duces the cellulase to be studied. Then, if the amino acid sequence of the cellulase is known, homologous, labelled oligonucleotide probes may be synthesized and used to ident¬ ify cellulase-encoding clones from a genomic library of bac¬ terial DNA, or from a fungal cDNA library. Alternatively, a labelled oligonucleotide probe containing sequences homolo¬ gous to cellulase from another strain of bacteria or fungus could be used as a probe to identify cellulase-encoding clo¬ nes, using hybridization and washing conditions of lower stringency.

Yet another method for identifying cellulase-producing clo- nes would involve inserting fragments of genomic DNA into an expression vector, such as a plasmid, transforming cellula- se-negative bacteria with the resulting genomic DNA library, and then plating the transformed bacteria onto agar contai¬ ning a substrate for cellulase. Those bacteria containing cellulase-bearing plasmid will produce colonies surrounded by a halo of clear agar, due to digestion of the substrate by secreted cellulase.

Alternatively, the DNA sequence encoding the enzyme may be prepared synthetically by established standard methods, e.g. the phosphoamidite method described by S.L. Beaucage and M.H. Caruthers, Tetrahedron Letters 22. 1981, pp. 1859-1869, or the method described by Matthes et al.. The EMBO J. 3. _/ 1984, pp. 801-805. According to the phosphoamidite method, oligonucleotides are synthesized, e.g. in an automatic DNA synthesizer, purified, annealed, ligated and cloned in appropriate vectors.

Finally, the DNA sequence may be of mixed genomic and syn¬ thetic, mixed synthetic and cDNA or mixed genomic and cDNA origin prepared by ligating fragments of synthetic, genomic or cDNA origin (as appropriate) , the fragments corresponding to various parts of the entire DNA sequence, in accordance with standard techniques. The DNA sequence may also be pre¬ pared by polymerase chain reaction (PCR) using specific pri¬ mers, for instance as described in US 4,683,202 or R.K. Sai- ki et al., Science 239. 1988, pp. 487-491.

Expression of cellulase variants

According to the invention, a mutated cellulase-coding sequ- ence produced by methods described above, or any alternative methods known in the art, can be expressed, in enzyme form, using an expression vector which typically includes control sequences encoding a promoter, operator, ribosome binding site, translation initiation signal, and, optionally, a re- pressor gene or various activator genes. To permit the se¬ cretion of the expressed protein, nucleotides encoding a "signal sequence" may be inserted prior to the cellulase- coding sequence. For expression under the direction of con¬ trol sequences, a target gene to be treated according to the invention is operably linked to the control sequences in the proper reading frame. Promoter sequences that can be incor¬ porated into plasmid vectors, and which can support the

transcription of the mutant cellulase gene, include but are not limited to the prokaryotic β-lactamase promoter (Villa- Ka aroff, et al., 1978, Proc. Natl. Acad. Sci. U.S.A. 25:3727-3731) and the tac promoter (DeBoer, et al., 1983, Proc. Natl. Acad. Sci. U.S.A. 8):21-25). Further references can also be found in "Useful proteins from recombinant bac¬ teria" in Scientific American, 1980, 242:74-94.

According to one embodiment B. subtilis is transformed by an expression vector carrying the mutated DNA. If expression is to take place in a secreting microorganism such as B. subti¬ lis a signal sequence may follow the translation initiation signal and precede the DNA sequence of interest. The signal sequence acts to transport the expression product to the cell wall where it is cleaved from the product upon secre¬ tion. The term "control sequences" as defined above is in¬ tended to include a signal sequence, when is present.

In a currently preferred method of producing cellulase vari- ants of the invention, a filamentous fungus is used as the host organism. The filamentous fungus host organism may con¬ veniently be one which has previously been used as a host for producing recombinant proteins, e.g. a strain of Asper- gillus sp. , such as A_j_ niger. A. nidulans or A _^ . oryzae. The use of Aj_ orvzae in the production of recombinant proteins is extensively described in, e.g. EP 238 023.

For expression of cellulase variants in Aspergillus, the DNA sequence coding for the cellulase variant is preceded by a promoter. The promoter may be any DNA sequence exhibiting a strong transcriptional activity in Aspergillus and may be derived from a gene encoding an extracellular or intracel- lular protein such as an amylase, a glucoamylase, a protea¬ se, a lipase, a cellulase or a glycolytic enzyme.

Examples of suitable promoters are those derived from the gene encoding A_j_ orvzae TAKA amylase, Rhizomucor miehei

aspartic proteinase, A _^. niger neutral α-amylase, A_j_ niger acid stable α-amylase, A _^. niger glucoamylase, Rhizomucor miehei lipase, A_j_ orvzae alkaline protease or A _^ _ oryzae triose phosphate isomerase.

In particular when the host organism is A _^ . oryzae. a prefer¬ red promoter for use in the process of the present invention is the A _^ _ orvzae TAKA amylase promoter as it exhibits a strong transcriptional activity in A _^ . orvzae. The sequence of the TAKA amylase promoter appears from EP 238 023.

Termination and polyadenylation sequences may suitably be derived from the same sources as the promoter.

The techniques used to transform a fungal host cell may suitably be as described in EP 238 023.

To ensure secretion of the cellulase variant from the host cell, the DNA sequence encoding the cellulase variant may be preceded by a signal sequence which may be a naturally oc¬ curring signal sequence or a functional part thereof or a synthetic sequence providing secretion of the protein from the cell. In particular, the signal sequence may be derived from a gene encoding an Aspergillus sp. amylase or glucoamy- lase, a gene encoding a Rhizomucor miehei lipase or protea¬ se, or a gene encoding a Humicola cellulase, xylanase or lipase. The signal sequence is preferably derived from the gene encoding A^. oryzae TAKA amylase, A_j_ niger neutral α- a ylase, A _. ;, niger acid-stable α-amylase or A_j_ niger gluco- amylase.

The medium used to culture the transformed host cells may be any conventional medium suitable for growing Aspergillus cells. The transformants are usually stable and may be cul- tured in the absence of selection pressure. However, if the transformants are found to be unstable, a selection marker introduced into the cells may be used for selection.

The mature cellulase protein secreted from the host cells may conveniently be recovered from the culture medium by well-known procedures including separating the cells from the medium by centrifugation or filtration, and precipitat- ing proteinaceous components of the medium by means of a salt such as ammonium sulphate, followed by chromatographic procedures such as ion exchange chromatography, affinity chromatography, or the like.

For example, EGI-Fus (from Fuεarium oxyεporum, Fig. 4) was produced by Aεpergilluε oryzae after transformation with a plasmid containing the disclosed sequence and using the nor¬ mal taka promotor and AMG terminator. Fermentation of the transformed A. oryzae strain gave a yield of 380 ECU per ml. The fermentation broth was purified by filtration and con¬ centration using ultrafiltration. The concentrate was ad¬ justed to pH 5 and applied to a high performance S-Sepharose column equilibrated with 50 mM sodium acetate, pH 5.0. The enzyme bound and was eluted with a sodium choride salt gra- dient. The pure endoglucanase (EGI-Fus) was eluted with 0.5 M sodium chloride.

Detergent Compositions

According to the invention, the cellulase of the invention or an endoglucanase derived from a strain of Humicola inεo¬ lenε and having the amino acid sequence listed in Figure 1 and an apparent molecular weight of about 50 kD measured in SDS-PAGE may typically be a component of a detergent co po- sition. As such, it may be included in the detergent compo¬ sition in the form of a non-dusting granulate, a stabilized liquid, or a protected enzyme. Non-dusting granulates may be produced, e.g., as disclosed in US 4,106,991 and 4,661,452 (both to Novo Industri A/S) and may optionally be coated by methods known in the art. Examples of waxy coating materials are poly(ethylene oxide) products (polyethyleneglycol, PEG) with mean molar weights of 1000 to 20000, ethoxylated nonyl-

phenols having from 16 to 50 ethylene oxide units; ethoxyla- ted fatty alcohols in which the alcohol contains from 12 to 20 carbon atoms and in which there are 15 to 80 ethylene oxide units; fatty alcohols; fatty acids; and mono- and di- and triglycerides of fatty acids. Examples of film-forming coating materials suitable for application by fluid bed techniques are given in patent GB 1483591. Liquid enzyme preparations may, for instance, be stabilized by adding a polyol such as propylene glycol, a sugar or sugar alcohol, lactic acid or boric acid according to established methods. Other enzyme stabilizers are well known in the art. Protec¬ ted enzymes may be prepared according to the method disclo¬ sed in EP 238,216. Accordingly, the present invention further relates to a detergent additive comprising a cellu- lase of the present invention or an endoglucanase derived from a strain of Humicola inεolenε and having the amino acid sequence listed in Figure 3 and an apparent molecular weight of about 50 kD measured in SDS-PAGE.

The detergent composition of the invention may be in any convenient form, e.g. as powder, granules, paste or liquid. A liquid detergent may be aqueous, typically containing up to 70% water and 0-30% organic solvent, or nonaqueous.

The detergent composition comprises one or more surfactants, each of which may be anionic, nonionic, cationic, or zwit- terionic. The detergent will usually contain 0-50% of anio¬ nic surfactant such as linear alkylbenzenesulfonate (LAS) , alpha-olefinsulfonate (AOS) , alkyl sulfate (fatty alcohol sulfate) (AS) , alcohol ethoxysulfate (AEOS or AES) , secon¬ dary alkanesulfonates (SAS) , alpha-sulfo fatty acid methyl esters, alkyl- or alkenylsuccinic acid, or soap. It may also contain 0-40% of nonionic surfactant such as alcohol ethoxy- late (AEO or AE) , carboxylated alcohol ethoxylates, nonyl- phenol ethoxylate, alkylpolyglycoside, alkyldimethylamine - oxide, ethoxylated fatty acid monoethanolamide, fatty acid

monoethanolamide, or polyhydroxy alkyl fatty acid amide (e.g. as described in WO 92/06154) .

The detergent composition may additionally comprise one or more other enzymes, such as amylase, lipase, cutinase, pro¬ tease, other cellulases, peroxidase, and oxidase, e.g., lac- case) .

The detergent may contain 1-65% of a detergent builder or complexing agent such as zeolite, diphosphate, triphosphate, phosphonate, citrate, nitrilotriacetic acid (NTA) , ethylene- diaminetetraacetic acid (EDTA) , diethylenetriaminepentaace- tic acid (DTMPA) , alkyl- or alkenylsuccinic acid, soluble silicates or layered silicates (e.g. SKS-6 from Hoechst) . The detergent may also be unbuilt, i.e. essentially free of detergent builder.

The detergent may comprise one or more polymers. Examples are carboxymethylcellulose (CMC) , poly(vinylpyrrolidone) (PVP) , polyethyleneglycol (PEG) , poly(vinyl alcohol) (PVA) , polycarboxylates such as polyacrylates, maleic/acrylic acid copolymers and lauryl methacrylate/acrylic acid copolymers.

The detergent may contain a bleaching system which may com- prise a H ₂ 0 ₂ source such as perborate or percarbonate which may be combined with a peracid-forming bleach activator such as tetraacetylethylenediamine (TAED) or nonanoyloxybenzene- sulfonate (NOBS) . Alternatively, the bleaching system may comprise peroxyacids of, e.g., the amide, i ide, or sulfone type.

The enzymes of the detergent composition of the invention may be stabilized using conventional stabilizing agents, e.g. a polyol such as propylene glycol or glycerol, a sugar or sugar alcohol, lactic acid, boric acid, or a boric acid derivative such as, e.g., an aromatic borate ester, and the

composition may be formulated as described in, e.g., WO 92/19709 and WO 92/19708.

The detergent may also contain other conventional detergent ingredients such as, e.g., fabric conditioners including clays, foam boosters, suds suppressors, anti-corrosion agents, soil-suspending agents, anti-soil-redeposition agents, dyes, bactericides, optical brighteners, or perfume.

The pH (measured in aqueous solution at use concentration) will usually be neutral or alkaline, e.g. in the range of 7- 11.

Particular forms of detergent compositions within the scope of the invention include:

1) A detergent composition formulated as a granulate having a bulk density of at least 600 g/1 comprising

2) A detergent composition formulated as a granulate having a bulk density of at least 600 g/1 comprising

3) A detergent composition formulated as a granulate having a bulk density of at least 600 g/1 comprising

4) A detergent composition formulated as a granulate having a bulk density of at least 600 g/1 comprising

6) An aqueous structured liquid detergent composition com¬ prising

7) A detergent composition formulated as a granulate having a bulk density of at least 600 g/1 comprising

8) A detergent composition formulated as a granulate compri- sing

9) A detergent composition formulated as a granulate compri¬ sing

10) An aqueous liquid detergent composition comprising

11) An aqueous liquid detergent composition comprising

12) A detergent composition formulated as a granulate ha¬ ving a bulk density of at least 600 g/1 comprising

13) Detergent formulations as described in 1) - 12) wherein all or part of the linear alkylbenzenesulfonate is replaced ^fa y (C ₁₂ —C ₁₈ ) alkyl sulfate.

514) A detergent composition formulated as a granulate ha¬ ving a bulk density of at least 600 g/1 comprising

5

15) A detergent composition formulated as a granulate ha¬ ving a bulk density of at least 600 g/1 comprising

16) Detergent formulations as described in 1) - 15) which contain a stabilized or encapsulated peracid, either as an additional component or as a substitute for already specifi¬ ed bleach systems.

17) Detergent compositions as described in 1) , 3) , 7) , 9) and 12) wherein perborate is replaced by percarbonate.

18) Detergent compositions as described in 1), 3), 7), 9), 12) , 14) and 15) which additionally contain a manganese ca¬ talyst. The manganese catalyst may, e.g., be one of the com- pounds described in "Efficient manganese catalysts for low- temperature bleaching", Nature 369, 1994, pp. 637-639.

19) Detergent composition formulated as a nonaqueous deter¬ gent liquid comprising a liquid nonionic surfactant such as, e.g., linear alkoxylated primary alcohol, a builder system

(e.g. phosphate), enzyme and alkali. The detergent may also comprise anionic surfactant and/or a bleach system.

The endoglucanase 'of the invention may be incorporated in concentrations conventionally employed in detergents. It is at present contemplated that, in the detergent composition of the invention, the endoglucanase may be added in an amount corresponding to 0.00001-1 mg (calculated as pure enzyme protein) of endoglucanase per liter of wash liquor.

In yet another aspect, the present endoglucanases may be used in fabric softeners, e.g. as described in Surfactant and Consumer Products, Ed. by J. Falbe, 1987, pp 295-296; Tenside Surfactants Detergents, 3J) (1993), 6, pp 394-399; JAOCS, Vol. 61 (1984), 2, pp 367-376; EP 517 762; EP 123 400; WO 92/19714; WO 93/19147; US 5,082,578; EP 494 769; EP 544 493; EP 543 562; US 5,235,082; EP 568 297; EP 570 237.

The present invention also relates to a washing process wherein soiled fabric is treated with a cellulase of the invention or an endoglucanase derived from a strain of Humi¬ cola inεolenε and having the amino acid sequence listed in Figure 3 and an apparent molecular weight of about 50 kD measured in SDS-PAGE.

It is contemplated that, dependent on the specificity of the modified cellulase, it may be employed for one or possibly more of the applications mentioned above, i.e. in the baking industry, in the wine and juice industry, for animal feed, and in textile and papermaking pulp processing. In a parti¬ cular embodiment, the enzyme preparation of the invention may comprise a combination of one or more modified cellula¬ ses with enzymes selected from the group consisting of un¬ modified or modified amylases, lipases, proteases, oxidore- ductases and hemicellulases.

Pulp and paper applications

In the papermaking pulp industry, the cellulase and/or en¬ zyme preparation according to the invention may be applied advantageously e.g. as follows:

- For debarking: pretreatment with the cellulase and/or en¬ zyme preparation according to the invention may degrade the cambium layer prior to debarking in mechanical drums resul- ting in advantageous energy savings.

- For defibration: treatment of a material containing cellu¬ losic fibers with the cellulase and/or enzyme preparation of the invention prior to refining or beating may result in reduction of the energy consumption due to the hydrolysing effect of the cellulase on the interfibre surfaces. Use of the cellulase and/or enzyme preparation of the invention may result in improved energy savings as compared to the use of unmodified enzymes, since it is believed that the modified cellulase may possess a higher ability to penetrate fibre walls.

- For fibre modification, i.e. improvement of fibre proper¬ ties where partial hydrolysis across the fibre wall is nee- ded which requires deeper penetrating enzymes (e.g. in or¬ der to make coarse fibers more flexible) . Deep treatment of fibers has so far not been possible for high yield pulps e.g. mechanical pulps or mixtures of recycled pulps. This has been ascribed to the nature of the fibre wall structure that prevents the passage of enzyme molecules due to physi¬ cal restriction of the pore matrix of the fibre wall. It is contemplated that the modified (i.e. derivatised) cellulases of the invention are capable of penetrating into the fibre wall.

- For drainage improvement. The drainability of papermaking pulps may be improved by treatment of the pulp with hydroly-

sing enzymes, e.g. cellulases. Use of the modified cellulase and/or enzyme preparation according to the invention may be more effective, e.g. result in a higher degree of loosening bundles of strongly hydrated micro-fibrils in the fines fraction (consisting of fibre debris) that limits the rate of drainage by blocking hollow spaces between fibers and in the wire mesh of the paper machine. The Canadian standard freeness (CSF) increases and the Schopper-Riegler drainage index decreases when pulp in subjected to cellulase treat- ment, see e.g. US patent 4,923,565; TAPPI T227, SCAN C19:65 which are hereby incorporated by reference.

- For inter fibre bonding. Hydrolytic enzymes are applied in the manufacture of papermaking pulps for improving the inter fibre bonding. The enzymes rinse the fibre surfaces for im¬ purities e.g. cellulosic debris, thus enhancing the area of exposed cellulose with attachment to the fibre wall, thus improving the fibre-to-fibre hydrogen binding capacity. This process is also referred to as dehornification. Paper and board produced with a cellulase containing enzyme prepara¬ tion according to the invention may have an improved strength or a reduced grammage, a smoother surface and an improved printability. These improvements are believed to be a result of the improved penetrability of the modified/der- ivatised enzyme(s).

- For enzymatic deinking. Partial hydrolysis of recycled paper during or upon pulping by use of hydrolysing enzymes such as cellulases are known to facilitate the removal and agglomeration of ink particles. Use of a modified cellulase and/or enzyme preparation according to the invention may give a more effective loosening of ink from the surface structure due to a better penetration of the enzyme molecu¬ les into the fibrillar matrix of the fibre wall, thus softe- ning the surface whereby ink particles are effectively loo¬ sened. The agglomeration of loosened ink particles are also improved, due to a more efficient hydrolysis of cellulosic

fragments found attached to ink particles originating from the fibres.

The treatment of lignocellulosic pulp may, e.g., be perfor- med as described in WO 91/14819, WO 91/14822, WO 92/17573 and WO 92/18688.

Textile applications

In another embodiment, the present invention relates to use of the modified cellulase and/or enzyme preparation accor¬ ding to the invention in the bio-polishing process. Bio-Po¬ lishing is a specific treatment of the yarn surface which improves fabric quality with respect to handle and appearan¬ ce without loss of fabric wettability. The most important effects of Bio-Polishing can be characterized by less fuzz and pilling, increased gloss/luster, improved fabric handle, increased durable softness and altered water absorbency. Bio-Polishing usually takes place in the wet processing of the manufacture of knitted and woven fabrics. Wet proces¬ sing comprises such steps as e.g. desizing, scouring, blea¬ ching, washing, dying/printing and finishing. During each of these steps, the fabric is more or less subjected to me- chanical action. In general, after the textiles have been knitted or woven, the fabric proceeds to a desizing stage, followed by a scouring stage, etc. Desizing is the act of removing size from textiles. Prior to weaving on mechanical looms, warp yarns are often coated with size starch or starch derivatives in order to increase their tensile strength. After weaving, the size coating must be removed before further processing the fabric in order to ensure a homogeneous and wash-proof result. It is known that in order to achieve the effects of Bio-Polishing, a combination of cellulolytic and mechanical action is required. It is also known that "super-softness" is achievable when the treatment with cellulase is combined with a conventional treatment

with softening agents. It is contemplated that use of the modified cellulase and/or enzyme preparation of the inven¬ tion for bio-polishing of cellulosic fabrics is advantage¬ ous, e.g. a more thorough polishing can be achieved. Bio- polishing may be obtained by applying the method described e.g. in WO 93/20278.

Degradation of plant material

In yet another embodiment, the present invention relates to use of a modified cellulase and/or enzyme preparation accor¬ ding to the invention for degradation of plant material e.g. cell walls.

It is contemplated that the modified cellulase and/or enzyme preparation of the invention is useful in the preparation of wine, fruit or vegetable juice in order to increase yield. Cellulases according to the invention may also be applied for enzymatic hydrolysis of various plant cell-wall derived materials or waste materials, e.g. agricultural residues such as wheat-straw, corn cobs, whole corn plants, nut shells, grass, vegetable hulls, bean hulls, spent grains, sugar beet pulp, and the like. The plant material may be degraded in order to improve different kinds of processing, facilitate purification or extraction of other components like purification of beta-glucan or beta-glucan oligomers from cereals, improve the feed value, decrease the water binding capacity, improve the degradability in waste water plants, improve the conversion of e.g. grass and corn to ensilage, etc.

In a preferred embodiment of the invention, the cellulase is an endoglucanase. The cellulolytic activity of endoglucanase is determined relative to an analytical standard and may be expressed in the unit ECU.

Cellulolytic enzymes hydrolyse CMC, thereby decreasing the viscosity of the incubation mixture. The resulting reduction in viscosity may be determined by a vibration viscosimeter (e.g. MIVI 3000 from Sofraser, France) .

Determination of the cellulolytic activity, measured in terms of ECU, may be determined according to the analysis method AF 301.1 which is available from the Applicant upon request.

The ECU assay quantifies the amount of catalytic activity present in the sample by measuring the ability of the sample to reduce the viscosity of a solution of carboxy- ethylcel- lulose (CMC) . The assay is carried out at 40°C, pH 7.5 using a relative enzyme standard for reducing the viscosity of the CMC substrate.

Cellulase activity on cellotriose

The cellulase activity on cellotriose, in terms of k^'S ^"1 , was determined by a coupled assay:

Cellotriose → Glucose + Cellobiose (cat.: cellulase)

Glucose + O ₂ + H ₂ O → Gluconate + H ₂ O ₂ (cat.: Glucoseoxidase)

H ₂ O ₂ + ABTS ^R → ABTS° ^X (cat.: Peroxidase)

which is followed spectrophotometrically at 418 nm (maximum absorbance of ABTS° ^X at 418 nm) .

Method:

The GOD-Perid Test Kit (available from Boehringer Mannheim, art. 124 036) was' used. The buffer-enzyme solution in the test kit was dissolved in 500 ml illi Q water. pH of the solution was adjusted to 8.5 (NaOH) .

80 mg of ABTS ^R (available from Boehringer Mannheim, art. 756 407) was dissolved in 10 ml GOD-Perid corresponding to a total concentration of ABTS ^R of 10 mg/ml.

A substrate stock solution of 5 mmole (2.52 mg/ml) of cello¬ triose (available from Merck art. 24741) in water was pre¬ pared. Diluted solutions in water corresponding to 1000 μ- mole, 500 μmole, 376 μmole, 250 μmole, lOOμmole and 60 μmole were prepared.

The reaction mixture was prepared by mixing 1 part of sub¬ strate solution with 1 part of GOD-Perid.

A solution of the cellulase enzyme to be determined in a concentration of 1.0 - 3.0 μmole was prepared.

50 μl of enzyme solution and 450 μl of reaction mixture were mixed.

The measurements were carried out on a HP 8452A Diode Array Spectrophotometer thermostated at 40°C, 1 cm cuvette, at a wavelength of 418 nm. The reaction was followed by measuring the oxidation af ABTS every 20 sec for 600 sec in total.

Calculationε:

The cellulase activity on cellotriose, in terms of k^-s ^"1 , was calculated from a Lineweaver-Burk plot (a plot of 1/V versus 1/[S]): the slope and the intersection were deter¬ mined by linear regression analysis.

The following constants were used for the calculations:

Cellulase: e = 66,310 M^cm' ¹ ABTS° ^X : e = 0.0323 μ ole ¹ *cm' ¹

For EG I' from Fuεarium oxyεporum (Figure 4), the catalytic activity on cellotriose at pH 8,5 and 40°C was calculated to 5,5 K _cat pr. sec. !(,„ was 0.5 mM.

Determination of alkaline cellulase activity on amorphous cellulose

Method:

Substrate preparation: 20 gram acid-swollen AVICEL ^* stock solution (see below for a preparation which can be stored for one month) was centrifuged for 20 min. at 5000 rpm. , the supernatant was poured off, and the sediment was resuspended in 30 ml of buffer. Then centrifuged for 20 min. at 5000 rp , the supernatant was poured off, and the sediment was resuspended in buffer to a total of 30 g.. This corresponds to a substrate concentration of 10 g AVICEL/litre.

Buffer: 0.1M Barbital at pH 8.5 or 0.1M Glycine at pH 10.0

Enzyme solution:

The enzymes were diluted to an activity of 0.5 S-CEVU/ml at pH 8.5 or 0.75 S-CEVU/ml at pH 10.0.

Reagents:

2% NaOH, PHBAH-reagent: 1.5 g of p-hydroxy benzoic acid hy- drazide and 5.0 g sodium tartrate was dissolved in 100 ml of 2% NaOH.

The substrate, the buffer and the enzyme solution were mixed as follows:

The substrate/buffer solution was preheated for 5 min at

40°C. Then the enzyme solution was added and the solution was whirlmixed for 5 sec. , followed by incubation for 20 min. at 40"C. The reaction was stopped by adding 500 μl 2% NaOH solution, followed by whirlmixing for 5 sec.

The samples were centrifuged for 20 min. at 5000 rpm.

1000 μl of supernatant was transferred from the test tubes to new test tubes, and 500 μl PHBAH-reagent was added, fol- lowed by boiling for 10 min.

The test tubes were cooled in ice water.

The absorbance of the samples were measured on a spectropho- tometer at 410 nm.

Standard glucose curve:

A stock solution containing 300 mg/1 was diluted to 5, 10, 15 and 25 mg/1.

1000 μl of the diluted standards were mixed with 500 μl of PHBAH-reagent, and were treated as the other samples, see above.

Determination of activity.

The release of reducing glucose equivalent was calculated using the standard curve.

The enzyme concentration was calculated using the molar ab- 5 sorbance of 66310 (e)for the EG I endoglucanase. The K,„ , V _max and K _cal was calculated from a Lineweaver-Burk plot using different substrate concentrations.

The molar absorbance of the cellulase variants having sub¬ stituted tyrosines and tryptophanes was adjusted accordingly lousing a absorbance value for tryptophane of 5690(e) and for tyrosine of 1280(e) and cystein 120(e).

The extinction coefficients (e) are disclosed in Gill,S.C. and Hippel, P.H. : Calculation of protein extinction coeffi- 15 cients from amino acid sequence data; Analytical Biochemi¬ stry vol 182, (319-326) , (1989) .

Each of the tested cellulases was purified to high homoge¬ neity giving a single band in SDS-PAGE analysis (the ratio 20 A ₂₈₀ /A ₂₆₀ was checked as being above 1.5).

Preparation of Acid swollen cellulose:

Materials: 255 g Avicel ^* . (Art. 2331 Merck)

150 ml 85% Ortho-phosphoric-acid. (Art. 573 Merck) 400 ml Acetone. (Art. 14 Merck) 1.3 1 Deionized water (Milli Q)

1 1 glass beaker

301 1 glass filter funnel

2 1 suction flask Ultra Turrax Homogenizer

Procedure: 35 The Acetone and the phosphoric-acid was cooled on ice.

The 5 g. Avicel ^* was moistened with water, then 150 ml of ice cold 85% Ortho-phosphoric-acid was added, and the mix¬ ture was placed on ice bath with weak stirring for 1 h. 100 ml of ice cold acetone was added with stirring, followed by transfer of the mixture to a glass filter funnel, follo¬ wed by washing with 3 x 100 ml ice cold acetone and dry suc¬ tion after each washing.

The filter cake was washed with 2 x 500 ml water and sucked as dry as possible after each wash. The filter cake was resuspended to a total volume of 300 ml and blended to homogeneity (using the Ultra Turrax Homogen- izer) . The resulting product was stored in a refrigerator.

The following result was obtained

EG I* from Humicola inεolenε (Figure 3) : k _cat at 8.5: 16 per sec k _cat at 10: 12 per sec

The extinction coefficient was 66310.

EGI-Fus from Fuεarium oxyεporum (Figure 4) : k _cat at 8.5, 40°C: 16 per sec (k,,, 8g/l) k _cat at 10, 40°C: 4 per sec (k.,, 8g/l)

The molar extinction coefficient was 58180, cal¬ culated based on the amino acid composition.

EXAMPLE 1

Mul i cycle terg-o-tometer test EG I* versus EG I

The example illustrates the superior soil removal effects of EG I* (truncated EG I, 402 amino acids, see Figure 3) versus EG I (415 amino acids, WO 91/17244 Fig. 14A-E) . In the

example EMPA 101 swatches have been used as soil removal tracers (carbon black/olive oil) .

The following detergent composition was used:

% by weight

LAS, (Nansa 1169/p) 10.3

AES, (Berol 452) 3.5

SOAP (C18) 0.5 SOAP (C14) 0.5

AEO (Dobanol 25-7) 6.4

Sodiumxylenesulfonat 5.1

Ethanol 0.7

MPG 2.7 Glycerol 0.5

Sodium sulphate 0.40

Sodium carbonate 2.7

Sodium citrate 4.4

Citric acid 1.5 Water Rest

Testing procedure

The test was based on a 2 cycle wash test in a terg-o-tome- ter using the detergent composition described above in a 0.3% solution with ImM Ca++.

Agitation 150 m/min Temperature 40°C pH 8.2

Swatches EMPA 101

(2 swatches a 5X6 cm pr 100 ml)

Washing time 20 minutes Rinse 10 minutes in tapwater Drying Line drying at room temperature

Repetitions 2

Result

The soil removal result is given as Delta remmision R (Enzy¬ me-treated versus blind) measured at 420 nm with an Elrepho apparatus (DataColor) .

Enzyme R (S.D.) Delta R

No enzyme 41.99 (0.41) 0

EG I, 4 ECU/1 42.00 (0.28) 0.01

EG I, 8 ECU/1 41.24 (0.45) -0.75

EG I, 12 ECU/1 42.69 (0.32) 0.71

EG I, 20 ECU/1 43.05 (0.32) 1.06

EG I*, 4 ECU/1 41.61 (0.37) -0.38

EG I*, 8 ECU/1 43.41 (0.39) 1.42

EG I*, 12 ECU/1 44.29 (0.35) 2.30

EG I*, 20 ECU/1 44.34 (0.47) 2.35

EXAMPLE 2

Carbon dispersing effect of EG I ^*

The particulate soil removing effect of endoglucanases is expected partly to be ascribed to the cleavage of glycosidic bonds in the cellulose matrix, but to some extent the enzyme may also provide a more non-specific cleaning effect, for instance, by improving the dispersability of the particulate soil.

In this test it is shown that EG I* (truncated EG I, 402 amino acids, see Figure 3) differs from EG I (415 amino acids, WO 91/17244 Fig. 14A-E) with respect to its ability to disperse active carbon.

Different amounts of purified EG I and EG I* were added into 10ml of a lg/1 suspension of active carbon (Norit) in lOmM Phosphate buffer, pH 10. The mixtures were incubated for 30 minutes at 55°C and 150 rpm.

After incubation the samples were allowed to cool to ambient temperature and non-dispersed carbon was allowed to settle (no centrifugation) for 15 minutes. The amount of carbon that was dispersed was evaluated by measuring the OD _582nm of the supernatant (at 582nm was found a peak maximum most li¬ kely resulting from scattering) . Due to the nature of the experiment (inhomogeneous solutions, time dependence etc) , the absolute OD _582nm levels may vary among the tests carried out, whereas the relative levels usually may be conserved.

The table below show the results of obtained in the test:

0D(582nm)=0D _5g2nm (w th enzyme)-OD _582nm (w thout enzyme) OD _5g2nm (without enzyme)=0.716

The results show that EG I* differs significantly from EG I in terms of its carbon dispersion ability - at 5mg/l level the Δ0D(582nm) obtained with EG I* is four times as high as that obtained with EG I. Also it should be noted that the effect of EG I* is actually very large - the apparant level of detergency is increased by about 70% in the presence of lOmg/1 EG I*.

EXAMPLE 2

Tensile strength loss induced by cellulase

Cellulases used for soil removal in detergents often gives rise to an increased fabric wear. This can be observed through a reduced tensile strength of the fabric.

In the present example three cellulases are compared: Cellu- zyme ^* (a known commercial cellulase preparation) , EG I* from H. inεolenε (Figure 3) and EG I-Fus from Fuεarium (Figure 4) (both cellulases of the present invention) .

Celluzyme ^* is a multicomplex cellulase product from Humicola inεolenε used in detergents for soil removal and color cla¬ rification.

Experimental:

Buffer: 0.05 M Tris-HCl, pH 7.0, 1 mM CaCl ₂

Textile/cup: 4 pcs. a 5 x 25 cm; woven fabric (app. 18 g)

Dosage: 10000 ECU/1 of

Celluzyme®,

Humicola inεolenε EGI PPC 4192,

Fuεarium EGI-161294/MChr.

Volume: 100 ml Time: 7 days dark storage, 25 "C. Rinse: 10 min in deionized water.

Evaluation: Tensile strength is measured as wet pull on

Instron.

The following results were obtained:

% tensile strength loss

Blind (no cellulase) 0% ± 8% **) Celluzyme 41% H . inεolenε EG I* 8% Fuεarium EGI-Fus -4%

**) 0% pr. definition; 8% is relative standard deviation.

From the results it can be concluded that EG I* from H . in- εolenε and EGI-Fus from Fuεarium oxyεporum are effective for soil removal but their use do not result in significant tensile strength loss in textile fabric.