DE102018208446A1 - Improved washing performance with a new alpha-amylase from Fomes fomentarius (Ffo) - Google Patents

Abstract

The invention is in the field of enzyme technology. The invention relates to amylases which can be used in particular with regard to the use in detergents and cleaners, all sufficiently similar amylases with a correspondingly similar sequence according to SEQ ID NO. 1 or SEQ ID NO. 2 and their coding nucleic acids. The invention further relates to the preparation thereof and to processes for using these amylases, their use as such and compositions containing them, in particular washing and cleaning agents.

Description

The invention is in the field of enzyme technology. The invention relates to amylases which can be used in particular with regard to the use in detergents and cleaners, all sufficiently similar amylases with a correspondingly similar sequence according to SEQ ID NO. 1 or SEQ ID NO. 2 and their coding nucleic acids. The invention further relates to the preparation thereof and to processes for using these amylases, their use as such and compositions containing them, in particular washing and cleaning agents.

Amylases are among the most technically important enzymes. Their use for detergents and cleaning agents is established industrially and they are typically contained in modern, powerful detergents and cleaners. An amylase is an enzyme that catalyzes the hydrolysis of the internal α- (1-4) -gycosidic bonds of amylose, but not the cleavage of terminal or α- (1-6) -glycoside bonds. Amylases are therefore a group of esterases (E.C. 3.2.1.1.). Amylases catalyze the cleavage of starch, glycogen, and other oligo- and polysaccharides that have an α- (1-4) -glycoside bond. In this respect, amylases act against starch residues in the laundry and catalyze their hydrolysis (endohydrolysis). Amylases with broad substrate spectra are used in particular where inhomogeneous raw materials or substrate mixtures have to be reacted, that is to say, for example, in detergents and cleaners, since contaminations may consist of differently structured starch molecules and oligosaccharides. The amylases used in the washing or cleaning agents known from the prior art are usually of microbial origin and are generally derived from bacteria or fungi, for example the genera Bacillus, Pseudomonas, Acinetobacter, Micrococcus, Humicola, Trichoderma or Trichosporon, in particular Bacillus. Amylases are usually produced by biotechnological methods known per se by suitable microorganisms, for example by transgenic expression hosts of the genera Bacillus or by filamentous fungi.

The patent US 8512986 discloses amylase and its use in a starch liquefaction process wherein starch is degraded into small oligo- and / or polysaccharide fragments. Also the patents US 7407677 B2 and US 8852912 B2 disclose specific amylases and their fragments for use in detergents and cleaners.

Nonetheless, there remains a need for amylase variants that have altered biochemical properties and thereby provide improved performance in industrial applications.

Surprisingly, it has now been found that an amylase from Basidiomyceta, in particular Fomes fomentarius (Ffo), or a sufficiently similar amylase (based on the sequence identity), is particularly suitable for use in detergents or cleaners, since it has a broad spectrum of starch Substrates hydrolyzed under standard washing conditions.

The invention therefore relates to an amylase comprising an amino acid sequence which has at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 has indicated amino acid sequence over the entire length.

The invention also provides an amylase comprising an amino acid sequence which has at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 has indicated amino acid sequence over the entire length thereof, or variants thereof. The variants according to the invention are characterized in that they consist of an amylase which has an amino acid sequence with at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 amino acid sequence indicated over their entire length, are available as a starting molecule by one or multiple conservative amino acid substitution. Alternatively or additionally, the variants according to the invention are characterized in that they consist of an amylase which has an amino acid sequence with at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 comprises, as the starting molecule, fragmentation, deletion, insertion or substitution mutagenesis and an amino acid sequence extending over at least 396, 400, 410, 420, 430, 440, 450, 460, 470 , 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566, or 567 are consistent with the parent molecule.

Another object of the invention is a method for producing an amylase, comprising providing a Ausgangssamylase having at least 70% sequence identity to that shown in SEQ ID NO. 1 SEQ ID NO. 2, or variants of the parent amylase, the variants being as defined above.

An amylase within the meaning of the present patent application therefore comprises both the amylase as such and an amylase prepared by a process according to the invention. All statements on the amylase therefore relate both to the amylase as a substance and to the corresponding processes, in particular the production process of the amylase. One for the amino acid sequence according to SEQ ID NO. 1 or SEQ ID NO. 2 corresponding nucleotide sequence is shown in SEQ ID NO. 3 or SEQ ID NO. 4 indicated.

Further subject matters of the invention include nucleic acids coding for these amylases, amylases according to the invention or amylases according to the invention, and non-human host cells containing amylases or nucleic acids which encode these amylases.

The invention further relates to amylases comprising agents, in particular detergents and cleaners, washing and cleaning processes, and uses defined by the amylases described herein, wherein the amylases used in this case at least 70% sequence identity with the in SEQ ID NO. 1 or SEQ ID NO. 2 indicated amino acid sequence over the entire length or variants thereof are. The variants used here are characterized in that they consist of an amylase which has an amino acid sequence with at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 amino acid sequence indicated over their entire length, are available as a starting molecule by one or multiple conservative amino acid substitution. Alternatively or additionally, the variants used are characterized in that they consist of an amylase which has an amino acid sequence with at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 comprises, as the starting molecule, fragmentation, deletion, insertion or substitution mutagenesis and an amino acid sequence extending over at least 396, 400, 410, 420, 430, 440, 450, 460, 470 , 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566, or 567 are consistent with the parent molecule.

The present invention is based on the surprising finding of the inventors that an amylase according to the invention from Basidiomyceta, in particular Fomes fomentarius, which has an amino acid sequence identical to that described in SEQ ID NO. 1 or SEQ ID NO. 2 at least 70% identical amino acid sequence, which causes hydrolysis of a wide range of starch substrates under standard washing conditions. This is particularly surprising inasmuch as so far for none of the amylases from Basidiomyceta, in particular Fomes fomentarius, the use in detergents or cleaning agents has been described.

The amylases according to the invention have a high stability in detergents or cleaners, for example with respect to surfactants and / or bleaches and / or to temperature influences and / or acidic or alkaline conditions and / or to pH changes and / or to denaturing or oxidizing Agents and / or against proteolytic degradation and / or against a change in the redox ratios. Thus, with particularly preferred embodiments of the invention, performance-enhanced amylase variants are provided. Such advantageous embodiments of amylases according to the invention consequently enable improved wash results of starch-containing stains in a wide temperature range.

An amylase according to the invention has an enzymatic activity, that is to say it is capable of hydrolysing starch and oligosaccharides, in particular in a washing or cleaning agent. An amylase of the invention is therefore an enzyme which catalyzes the hydrolysis of α- (1-4) -glycoside bonds in glycoside substrates and thereby is capable of cleaving starch or oligosaccharides. Further, an amylase of the invention is preferably a mature amylase, i. to the catalytically active molecule without signal and / or propeptide (s). Unless otherwise stated, the sequences given refer to each mature (processed) enzymes. As used herein, SEQ ID NO. 1 shows the amino acid sequence of the mature protein, SEQ ID NO. 2 indicates the sequence including signal peptide.

"Amylase of the invention" as used herein refers to at least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81% of amylases. , 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92.5%, 93 %, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 98.6 %, 98.7%, 98.8%, 98.9%, 99%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8% or 99.9% sequence identity with the sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 indicated amino acid sequence over the entire length or variants thereof are. The Variants are characterized by being obtainable from an amylase having the indicated sequence identity as the parent molecule by one or more conservative amino acid substitutions. Alternatively or additionally, the variants used are characterized in that they are obtainable from an amylase having the stated sequence identity as the starting molecule by fragmentation, deletion, insertion or substitution mutagenesis and comprises an amino acid sequence which is at least 396, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566 or 567 contiguous amino acids matches the parent molecule.

In various embodiments of the invention, the amylase comprises an amino acid sequence identical to that shown in SEQ ID NO. 1 at least 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 98.8%, 99.0%, 99.2%, 99.4%, 99.5%, 99.6% or 99.8% is identical.

In other various embodiments of the invention, the amylase is a free enzyme. This means that the amylase can act directly with all components of an agent and, if the agent is a liquid agent, that the amylase is in direct contact with the solvent of the agent (e.g., water) of the invention. In other embodiments, the amylase of the invention may form an interaction complex with other molecules or contain an "envelope" in an agent. Here, a single or multiple amylase molecules may be separated from the other components of an agent by a surrounding structure. Such a separating structure may arise from, but is not limited to, vesicles such as a micelle or a liposome. The surrounding structure may also be a virus particle, a bacterial cell or a eukaryotic cell. In various embodiments, the amylase of the invention may be contained in Basidiomyceta cells expressing this amylase or in cell culture supernatants of such cells.

The identity of nucleic acid or amino acid sequences is determined by a sequence comparison. This sequence comparison is based on the BLAST algorithm established in the prior art and commonly used (cf., for example, US Pat Altschul, SF, Gish, W., Miller, W., Myers, EW & Lipman, DJ (1990): "Basic local alignment search tool", J. Mol. Biol. 215: 403-410 , and Altschul, Stephan F., Thomas L. Madden, Alejandro A. Schaffer, Jinghui Zhang, Hheng Zhang, Webb Miller, and David J. Lipman (1997): "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs Nucleic Acids Res. 25: 3389-3402 ) and in principle occurs in that similar sequences of nucleotides or amino acids in the nucleic acid or amino acid sequences are assigned to each other. A tabular assignment of the respective positions is referred to as alignment. Another algorithm available in the prior art is the FASTA algorithm. Sequence comparisons (alignments), in particular multiple sequence comparisons, are created with computer programs. Frequently used, for example, the Clustal series (see, for example Chenna et al. (2003): "Multiple sequence alignment with the Clustal series of programs", Nucleic Acids Res. 31: 3497-3500 ), T-Coffee (cf., for example Notredame et al. (2000): "T-Coffee: A novel method for multiple sequence alignments", J. Mol. Biol. 302: 205-217 ) or programs based on these programs or algorithms. Also possible are alignment comparisons (alignments) with the computer program Vector NTI® Suite 10.3 (Invitrogen Corporation, 1600 Faraday Avenue, Carlsbad, California, USA) with the default parameters whose AlignX module for sequence comparisons is based on ClustalW.

Such a comparison also allows a statement about the similarity of the compared sequences to each other. It is usually expressed in terms of percentage identity, that is to say the proportion of identical nucleotides or amino acid residues at the same or in an alignment with one another. The broader concept of homology involves conserved amino acid substitutions in amino acid sequences, that is, amino acids with similar chemical activity, as they usually perform similar chemical activities within the protein. Therefore, the similarity of the sequences compared can also be given as% homology or percent similarity. Identity and / or homology information can be made about whole polypeptides or genes or only over individual regions. Homologous or identical regions of different nucleic acid or amino acid sequences are therefore defined by matches in the sequences. Such areas often have identical functions. They can be small and comprise only a few nucleotides or amino acids. Often, such small regions exert essential functions for the overall activity of the protein. It may therefore be useful to relate sequence matches only to individual, possibly small areas. Unless otherwise indicated, identity or homology information in the present application, however, refers to the total length of the particular nucleic acid or amino acid sequence indicated.

In the context of the present invention, the statement that an amino acid position of a numerically designated position in SEQ ID NO. 1 therefore corresponds to the corresponding position of the numerically designated position in SEQ ID NO. 1 is assigned in an alignment as defined above.

In a further embodiment of the invention, the amylase is characterized in that its purification performance compared to that of an amylase comprising an amino acid sequence which corresponds to that in SEQ ID NO. 1 indicated amino acid sequences is not significantly reduced, i. has at least 70%, 75%, 80%, 85%, 90%, 95% of the reference washing performance. The cleaning performance can be determined in a washing system containing a detergent in a dosage between 4.5 and 7.0 grams per liter of wash liquor and the amylase, wherein the amylases to be compared are used in the same concentration (based on active protein) and the cleaning performance a soiling on cotton is determined by measuring the degree of cleaning of the washed textiles. For example, the washing process can be carried out for 60 minutes at a temperature of 40 ° C and the water has a water hardness between 5 ° and 25 °, preferably 10 ° and 20 °, more preferably 13 ° and 17 ° and further preferably 15.5 ° and 16, 5 ° (German hardness). The concentration of the amylase in the detergent intended for this washing system is from 0.001 to 1% by weight, preferably from 0.001 to 0.1% by weight, and more preferably from 0.01 to 0.06% by weight on active, purified protein.

A preferred liquid detergent for such a washing system is composed as follows (all figures in% by weight): 7% alkylbenzenesulfonic acid, 9% anionic surfactants, 4% Na salts of C ₁₂ -C ₁₈ fatty acids, 7% nonionic surfactants, 0.7% phosphonates, 3.2% citric acid, 3.0% NaOH, 0.04% defoamer, 5.7% 1,2-propanediol, 0.1% preservatives, 2% ethanol, 0.2% dye Transfer inhibitor, residual demineralized water. Preferably, the dosage of the liquid detergent is between 4.5 and 6.0 grams per liter of wash liquor, for example, 4.7, 4.9 or 5.9 grams per liter of wash liquor. Preference is given to washing in a pH range between pH 7.5 and pH 10.5, preferably between pH 7.5 and pH 9.

In the context of the invention, the determination of the cleaning performance at 40 ° C using a liquid detergent as stated above, wherein the washing process is preferably carried out for 60 minutes.

The degree of whiteness, i. the brightening of the stains, as a measure of the cleaning performance is determined by optical measurement methods, preferably photometrically. A suitable device for this purpose is for example the spectrometer Minolta CM508d. Usually, the devices used for the measurement are previously calibrated with a white standard, preferably a supplied white standard.

The activity-equivalent use of the respective amylase ensures that even if the ratio of active substance to total protein (the values of the specific activity) diverge, the respective enzymatic properties, for example the cleaning performance of certain soils, are compared. In general, a low specific activity can be compensated by adding a larger amount of protein.

The amylase activity is determined in a customary manner, preferably by an optical measuring method, preferably a photometric method. The appropriate test involves the amylase-dependent cleavage of the substrate para-nitrophenyl maltoheptaoside. This is cleaved by the amylase into para-nitrophenyl oligosaccharide. The para-nitrophenyl oligosaccharide is in turn catalyzed by the enzymes glucoamylase and alpha-glucosidase to glucose and para-nitrophenol. The presence of para-nitrophenol can be measured using a photometer, e.g. of the Tecan Sunrise device and the XFLUOR software, are determined at 405 nm and thus allows a conclusion on the enzymatic activity of the amylase.

The protein concentration can be determined by known methods, for example the BCA method (bicinchoninic acid, 2,2'-biquinolyl-4,4'-dicarboxylic acid) or the biuret method ( Gornall AG, CS Bardawill and MM David, J. Biol. Chem., 177 (1948), pp. 751-766 ). The determination of the active protein concentration can in this regard via a titration of the active sites using a suitable irreversible inhibitor and determination of the residual activity (see. Bender, M., et al., J. Am. Chem. Soc. 88, 24 (1966), p. 5890-5913 ) respectively.

Proteins can be grouped into groups of immunologically related proteins by reaction with an antiserum or antibody. The members of such a group are characterized by having the same antigenic determinant recognized by an antibody respectively. They are therefore structurally so similar to each other that they are recognized by an antiserum or specific antibodies. A further subject of the invention therefore forms amylases, which are characterized in that they have at least one and increasingly preferably two, three or four matching antigenic determinants with an amylase according to the invention. Due to their immunological similarity, such amylases are structurally so similar to the amylases according to the invention that a similar function can also be assumed.

Amylases according to the invention can be obtained in comparison to the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. Amylase described further amino acid changes, in particular amino acid substitutions, insertions or deletions exhibit. Such amylases are, for example, by targeted genetic modification, i. by mutagenesis, further developed and optimized for specific applications or specific properties (for example, in terms of catalytic activity, stability, etc.). Furthermore, nucleic acids according to the invention can be introduced into recombination approaches and thus used to generate completely novel amylases or other polypeptides.

The goal is to introduce into the known molecules targeted mutations such as substitutions, insertions or deletions, for example, to improve the cleaning performance of enzymes of the invention. For this purpose, in particular the surface charges and / or the isoelectric point of the molecules and thereby their interactions with the substrate can be changed. Thus, for example, the net charge of the enzymes can be changed in order to influence the substrate binding, in particular for use in detergents and cleaners. Alternatively or additionally, the stability of the amylase can be increased even further by one or more corresponding mutations, thereby improving its purification performance. Advantageous properties of individual mutations, e.g. individual substitutions can complement each other. An amylase which has already been optimized with regard to certain properties, for example with regard to its activity and / or its tolerance with regard to the substrate spectrum, can therefore be further developed within the scope of the invention.

For the description of substitutions that concern exactly one amino acid position (amino acid substitutions), the following convention is used: first, the naturally occurring amino acid is designated in the form of the international one-letter code, followed by the associated sequence position and finally the inserted amino acid. Several exchanges within the same polypeptide chain are separated by slashes. For insertions, additional amino acids are named after the sequence position. In the case of deletions, the missing amino acid is replaced by a symbol, for example a star or a dash, or a Δ is specified in front of the corresponding position. For example, R45Q describes the substitution of arginine at position 45 by glutamine, N45AQ the insertion of glutamine after the amino acid alanine at position 45 and N45 * or ΔN45 the deletion of asparagine at position 45. This nomenclature is known to those skilled in the art of enzyme technology.

Another object of the invention is therefore an amylase, which is characterized in that it is obtainable from an amylase as described above as the starting molecule by one or more conservative amino acid substitution. The term "conservative amino acid substitution" means the substitution of one amino acid residue for another amino acid residue, which exchange does not result in a change in polarity or charge at the position of the exchanged amino acid, eg, the replacement of a nonpolar amino acid residue with another nonpolar amino acid residue. Conservative amino acid substitutions within the scope of the invention include, for example: G = A = S, I = V = L = M, D = E, N = Q, K = R, Y = F, S = T, G = A = I = V = L = M = Y = F = W = P = S = T. In this case, the amylase may comprise an amino acid sequence before and, for example, even after the conservative amino acid substitution, which corresponds to the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. At least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, of the total amino acid sequence indicated. 84%, 85%, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92.5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 98.6%, 98.7%, 98.8%, 98.9%, 99.0%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8% or 99.9% is identical.

Alternatively or additionally, the amylase is characterized in that it is obtainable from an amylase as described above as starting molecule by fragmentation, deletion, insertion or substitution mutagenesis and comprises an amino acid sequence having a length of at least 396, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566, or 567 contiguous amino acids matches the parent molecule. In this case, the amylase before and, for example, even after fragmentation, deletion, insertion or substitution mutagenesis may comprise an amino acid sequence which corresponds to the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. At least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, of the total amino acid sequence indicated. 84%, 85%, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92.5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 98.6%, 98.7%, 98.8%, 98.9%, 99.0%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8% or 99.9% is identical.

Thus it is possible, for example, to delete individual amino acids at the termini or in the loops of the enzyme, without this losing or reducing the catalytic activity. Furthermore, such fragmentation, deletion, insertion or substitution mutagenesis can also reduce, for example, the allergenicity of the enzymes concerned and thus improve their overall applicability. Advantageously, even after mutagenesis, the enzymes retain their catalytic activity, i. their catalytic activity is at least equal to that of the starting enzyme, i. in a preferred embodiment, the catalytic activity is at least 80%, preferably at least 90% of the activity of the starting enzyme. Other substitutions can also show beneficial effects. Both single and multiple contiguous amino acids can be substituted for other amino acids.

The further amino acid positions are determined by an alignment of the amino acid sequence of an amylase according to the invention with the amino acid sequence of the amidase from Basidiomyceta, in particular Fomes fomentarius, as described in SEQ ID NO. 1 or SEQ ID NO. 2 is defined. Furthermore, the assignment of the positions depends on the mature (mature) protein. This assignment is also to be used in particular if the amino acid sequence of an amylase according to the invention comprises a higher number of amino acid residues than the amylase from Basidiomyceta, in particular Fomes fomentarius, according to SEQ ID NO. 1 or SEQ ID NO. 2. Starting from the above-mentioned positions in the amino acid sequence of the amidase from Basidiomyceta, in particular Fomes fomentarius, the change positions in an amylase according to the invention are those which are just assigned to these positions in an alignment.

Further confirmation of the correct assignment of the amino acids to be changed, ie in particular their functional correspondence, can provide comparative experiments, according to which the two positions assigned to each other on the basis of an alignment are changed in the same way in both amylases compared with each other and if both are observed the enzymatic activity is changed in the same way. If, for example, an amino acid exchange in a certain position of the amylase from Basidiomyceta, in particular Fomes fomentarius, according to SEQ ID NO. 1 or SEQ ID NO. 2 associated with a change in an enzymatic parameter, for example, with the increase of the K _M value, and a corresponding change in the enzymatic parameter, for example, also an increase in the K _M value, observed in an amylase variant according to the invention, the amino acid exchange by the same introduced amino acid has been achieved, a confirmation of the correct association is to be seen herein.

In particular, according to the invention, fragments of the amylase are also defined as herein, in particular those according to SEQ ID NO. 1, which are shortened at the N- and / or C-terminus such that one or more amino acids of the amylase, for example 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10, are no longer present, detected. Also of these truncated fragments variants can be used in various embodiments of the invention, which to the starting from in SEQ ID NO. 1 amino acid sequence shortened by (in each case) 1 to 10 N-terminal and / or C-terminal amino acids, over the total length to at least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77 %, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 90, 91, 91 , 5%, 92%, 92.5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5 %, 98%, 98.5%, 98.6%, 98.7%, 98.8%, 98.9%, 99.0%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8% or 99.9% are identical.

For example, according to the invention, amylases are also detected which have an amino acid sequence which, via the amylase, comprises an amino acid sequence which is at least 70%, preferably at least 80%, more preferably at least 95% sequence identity with the in SEQ ID NO. 1 amino acid sequence over the entire length thereof or the variants thereof described herein, goes out without thereby losing or reducing the catalytic activity. Preferably such amylases are those which have N- and / or C-terminal additional amino acids, for example the signal peptide or fragments of the signal peptide, whereby the signal peptide or the fragments of the signal peptide are formed in the production of the amylase.

According to the invention, amylases are also detected which have an amino acid sequence which is opposite to an amylase comprising an amino acid sequence which has at least 70%, preferably at least 80%, particularly preferably at least 95% sequence identity with the sequence shown in SEQ ID NO. 2 or the variants thereof described herein are shortened at the N-terminus such that the signal peptide or one or more amino acids of the signal peptide, for example 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 or 22, especially the N-terminal 22 amino acids are no longer included. Also of these amylases with the signal peptide or fragments of the signal peptide can be used in various embodiments of the invention, variants starting from the in SEQ ID NO. 2 amino acid sequence shortened by 1 to 22 N-terminal amino acids, over the total length to at least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80 %, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92, 5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5% , 98.6%, 98.7%, 98.8%, 98.9%, 99.0%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5% , 99.6%, 99.7%, 99.8% or 99.9% are identical.

All these facts are also applicable to the process of the invention for the preparation of an amylase.

1. a) Einbringen einer ein- oder mehrfachen konservativen Aminosäuresubstitution in eine Ausgangs-Amylase gemäß SEQ ID NO. 1 oder SED ID NO. 2;
2. b) Veränderung der in SEQ ID NO. 1 oder SED ID NO. 2 angegebenen Aminosäuresequenz durch Fragmentierung, Deletions-, Insertions- oder Substitutionsmutagenese derart, dass die Amylase eine Aminosäuresequenz umfasst, die über eine Länge von mindestens 396, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566 oder 567 zusammenhängenden Aminosäuren mit dem Ausgangsmolekül übereinstimmt.

Accordingly, a method according to the invention comprises a method for the production of an amylase, comprising the provision of an initial amylase which has at least 70%, preferably at least 80%, particularly preferably at least 95% sequence identity to that shown in SEQ ID NO. 1 or SEQ ID NO. 2, or variants of the starting amylase, wherein the method according to the invention for producing the variants comprises, for example, one or more of the following method steps:

1. a) introduction of a single or multiple conservative amino acid substitution into an initial amylase according to SEQ ID NO. 1 or SED ID NO. 2;
2. b) modification of SEQ ID NO. 1 or SED ID NO. 2 amino acid sequence by fragmentation, deletion, insertion or substitution mutagenesis such that the amylase comprises an amino acid sequence having a length of at least 396, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566 or 567 contiguous amino acids matches the parent molecule.

All embodiments also apply to the inventive method.

In further embodiments of the invention, the amylase or the amylase prepared by a process according to the invention is still at least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 90, 91, 91, 92, 92, 92 , 5%, 93%, 93.5%, 94%, 94.5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5 %, 98.6%, 98.7%, 98.8%, 98.9%, 99.0%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5% %, 99.6%, 99.7%, 99.8% or 99.9% identical to that shown in SEQ ID NO. 1 indicated amino acid sequence over the entire length.

Another object of the invention is a previously described amylase, which is additionally stabilized, in particular by one or more mutations, for example substitutions, or by coupling to a polymer. An increase in stability during storage and / or during use, for example in the washing process, leads to longer enzymatic activity and thus improves cleaning performance. In principle, all stabilization options described in the prior art and / or appropriate considerations come into consideration. Preference is given to those stabilizations which are achieved by mutations of the enzyme itself, since such stabilizations do not require any further working steps following the recovery of the enzyme. Examples of sequence changes suitable for this purpose are mentioned above. Other suitable sequence changes are known from the prior art.

• - Schutz gegen den Einfluss von denaturierenden Agentien wie Tensiden durch Mutationen, die eine Veränderung der Aminosäuresequenz auf oder an der Oberfläche des Proteins bewirken;
• - Austausch von Aminosäuren, die nahe dem N-Terminus liegen, gegen solche, die vermutlich über nicht-kovalente Wechselwirkungen mit dem Rest des Moleküls in Kontakt treten und somit einen Beitrag zur Aufrechterhaltung der globulären Struktur leisten.

Options for stabilization include:

• Protection against the influence of denaturing agents, such as surfactants, on mutations causing an alteration of the amino acid sequence on or at the surface of the protein;
• Replacement of amino acids located near the N-terminus against those likely to contact non-covalent interactions with the rest of the molecule, thus contributing to the maintenance of the globular structure.

Preferred embodiments are those in which the enzyme is stabilized in several ways, as several stabilizing mutations act additive or synergistic.

Another object of the invention is an amylase as described above, which is characterized in that it has at least one chemical modification. An amylase with such a change is called a derivative, ie the amylase is derivatized.

For the purposes of the present application, derivatives are understood as meaning those proteins whose pure amino acid chain has been chemically modified. Such derivatizations can be done, for example, in vivo by the host cell expressing the protein. In this regard, couplings of low molecular weight compounds such as lipids or oligosaccharides are particularly noteworthy. However, derivatizations can also be carried out in vitro, for example by the chemical transformation of a side chain of an amino acid or by covalent binding of another compound to the protein. For example, the coupling of amines to carboxyl groups of an enzyme to alter the isoelectric point is possible. Such another compound may also be another protein that is bound to a protein of the invention via bifunctional chemical compounds, for example. Similarly, derivatization is to be understood as meaning the covalent binding to a macromolecular carrier, or else a noncovalent inclusion in suitable macromolecular cage structures. Derivatizations may, for example, affect the substrate specificity or binding strength to the substrate or cause a temporary blockage of the enzymatic activity when the coupled substance is an inhibitor. This can be useful, for example, for the period of storage. Such modifications may further affect stability or enzymatic activity. They can also serve to reduce the allergenicity and / or immunogenicity of the protein and thus, for example, increase its skin compatibility. For example, couplings with macromolecular compounds, for example, polyethylene glycol, can improve the protein in terms of stability and / or skin tolerance.

Derivatives of a protein according to the invention can also be understood in the broadest sense to mean preparations of these proteins. Depending on the extraction, processing or preparation, a protein may be associated with various other substances, for example from the culture of the producing microorganisms. A protein may also have been deliberately added to other substances, for example to increase its storage stability. Therefore, all preparations of a protein according to the invention are also according to the invention. This is also independent of whether or not it actually exhibits this enzymatic activity in a particular preparation. Because it may be desired that it has no or only low activity during storage, and unfolds its enzymatic function only at the time of use. This can be controlled, for example, via appropriate accompanying substances. In particular, the joint preparation of amylases with specific inhibitors is possible in this regard.

With regard to all the amylases or amylase variants and / or derivatives described above, particular preference is given in the context of the present invention to those whose catalytic activity and / or their substrate tolerance correspond to those of the amylase according to SEQ ID NO. 1, the catalytic activity and substrate tolerance being determined as described above.

A further subject of the invention is a nucleic acid which codes for an amylase according to the invention, as well as a vector containing such a nucleic acid, in particular a cloning vector or an expression vector. In preferred embodiments, the nucleic acid is a nucleic acid according to SEQ ID NO. 3 or SEQ ID NO. 4. Accordingly, a particularly preferred vector according to the invention is a vector which comprises a nucleic acid according to SEQ ID NO. 3 or SEQ ID NO. 4 includes.

These may be DNA or RNA molecules. They can be present as a single strand, as a single strand that is complementary to this single strand, or as a double strand. Especially in the case of DNA molecules, the sequences of both complementary strands must be taken into account in all three possible reading frames. Furthermore, it should be noted that different codons, so base triplets, can code for the same amino acids, so that a particular amino acid sequence can be encoded by several different nucleic acids. Due to this degeneracy of the genetic code, all nucleic acid sequences are included in this subject of the invention which can encode any of the above-described amylases. The person skilled in the art is able to determine these nucleic acid sequences unequivocally since, despite the degeneracy of the genetic code, individual codons are assigned defined amino acids. Therefore, the person skilled in the art can easily determine nucleic acids coding for this amino acid sequence on the basis of an amino acid sequence. Furthermore, with nucleic acids according to the invention, one or more codons may be replaced by synonymous codons. This aspect relates in particular to the heterologous expression of the enzymes according to the invention. Thus, each organism, for example a host cell of a production strain, has a particular codon usage. Codon usage is the translation of the genetic code into amino acids by the particular organism Roger that. Bottlenecks in protein biosynthesis can occur if the codons lying on the nucleic acid in the organism face a comparatively small number of loaded tRNA molecules. Although coding for the same amino acid, this results in a codon being translated less efficiently in the organism than a synonymous codon encoding the same amino acid. Due to the presence of a higher number of tRNA molecules for the synonymous codon, it can be more efficiently translated in the organism.

A person skilled in the art can use well-known methods such as chemical synthesis or the polymerase chain reaction (PCR) in combination with molecular biological and / or proteinchemical standard methods, using known DNA and / or amino acid sequences, the corresponding nucleic acids to complete genes manufacture. Such methods are for example Sambrook, J., Fritsch, EF and Maniatis, T. 2001. Molecular cloning: a laboratory manual, 3rd Edition Cold Spring Laboratory Press , known.

For the purposes of the present invention, vectors are understood as consisting of nucleic acids which contain a nucleic acid according to the invention as a characteristic nucleic acid region. They can establish these in a species or cell line over several generations or cell divisions as a stable genetic element. Vectors, especially when used in bacteria, are special plasmids, ie circular genetic elements. In the context of the present invention, a nucleic acid according to the invention is cloned into a vector. The vectors include, for example, those whose origin are bacterial plasmids, viruses or bacteriophages, or predominantly synthetic vectors or plasmids with elements of various origins. With the other genetic elements present in each case, vectors are able to establish themselves as stable units in the relevant host cells over several generations. They may be extrachromosomal as separate units or integrated into a chromosome or chromosomal DNA.

Expression vectors comprise nucleic acid sequences which enable them to replicate in the host cells containing them, preferably microorganisms, particularly preferably bacteria, and to express a contained nucleic acid there. In particular, expression is influenced by the promoter (s) that regulate transcription. In principle, the expression may be effected by the natural promoter originally located in front of the nucleic acid to be expressed, but also by a promoter of the host cell provided on the expression vector or also by a modified or completely different promoter of another organism or another host cell. In the present case, at least one promoter for the expression of a nucleic acid according to the invention is made available and used for its expression. Furthermore, expression vectors can be regulatable, for example by changing the culturing conditions or when a specific cell density of the host cells contained therein is reached or by addition of specific substances, in particular activators of gene expression. An example of such a substance is the galactose derivative isopropyl-β-D-thiogalactopyranoside (IPTG), which is used as an activator of the bacterial lactose operon (lac operon). In contrast to expression vectors, the nucleic acid contained is not expressed in cloning vectors.

A further subject of the invention is a non-human host cell which contains a nucleic acid according to the invention or a vector according to the invention, or which contains an amylase according to the invention, in particular one which secretes the amylase into the medium surrounding the host cell. Preferably, a nucleic acid according to the invention or a vector according to the invention is transformed into a microorganism, which then represents a host cell according to the invention. Alternatively, individual components, ie nucleic acid parts or fragments of a nucleic acid according to the invention can be introduced into a host cell such that the resulting host cell contains a nucleic acid according to the invention or a vector according to the invention. This procedure is particularly suitable when the host cell already contains one or more constituents of a nucleic acid according to the invention or a vector according to the invention and the further constituents are then supplemented accordingly. Methods of transforming cells are well established in the art and well known to those skilled in the art. In principle, all cells, that is to say prokaryotic or eukaryotic cells, are suitable as host cells. Preference is given to those host cells which can be handled genetically advantageously, for example as regards the transformation with the nucleic acid or the vector and its stable establishment, for example unicellular fungi or bacteria. Furthermore, preferred host cells are characterized by good microbiological and biotechnological handling. This concerns, for example, easy culturing, high growth rates, low demands on fermentation media and good production and secretion rates for foreign proteins. Preferred host cells according to the invention secrete the (transgenially) expressed protein into the medium surrounding the host cells. Further, the amylases may be derived from the cells producing them after their production modified, for example, by attachment of sugar molecules, formylations, aminations, etc. Such post-translational modifications may functionally affect the amylase.

Further preferred embodiments are those host cells which are regulatable in their activity due to genetic regulatory elements which are provided, for example, on the vector, but may also be present in these cells from the outset. For example, by controlled addition of chemical compounds that serve as activators, by changing the culture conditions or when reaching a specific cell density, these can be excited for expression. This enables an economical production of the proteins according to the invention. An example of such a compound is IPTG as described above.

Preferred host cells are prokaryotic or bacterial cells. Bacteria are characterized by short generation times and low demands on cultivation conditions. As a result, inexpensive cultivation methods or production methods can be established. In addition, the expert has a wealth of experience in bacteria in fermentation technology. For a specific production, gram-negative or gram-positive bacteria may be suitable for a wide variety of reasons to be determined experimentally in individual cases, such as nutrient sources, product formation rate, time requirement, etc.

In Gram-negative bacteria, such as Escherichia coli, a large number of proteins are secreted into the periplasmic space, ie into the compartment between the two membranes enclosing the cells. This can be advantageous for special applications. Furthermore, Gram-negative bacteria can also be designed such that they eject the expressed proteins not only into the periplasmic space but into the medium surrounding the bacterium. In contrast, gram-positive bacteria such as Bacilli or Actinomycetes or other representatives of Actinomycetales have no outer membrane, so that secreted proteins are released immediately into the medium surrounding the bacteria, usually the nutrient medium, from which the expressed proteins can be purified. They can be isolated directly from the medium or further processed. In addition, Gram-positive bacteria are related or identical to most of the organisms of origin for technically important enzymes and usually form even comparable enzymes, so they have a similar codon use and their protein synthesizer is naturally aligned accordingly.

Host cells according to the invention may be altered in their requirements of the culture conditions, have different or additional selection markers or express other or additional proteins. In particular, it may also be those host cells which express several proteins or enzymes transgene.

The present invention is applicable in principle to all microorganisms, in particular to all fermentable microorganisms, particularly preferably those of the genus Bacillus, and results in the production of proteins according to the invention by the use of such microorganisms. Such microorganisms then represent host cells in the sense of the invention.

In a further embodiment of the invention, the host cell is characterized in that it is a bacterium, preferably one selected from the genera of Escherichia, Klebsiella, Bacillus, Staphylococcus, Corynebacterium, Arthrobacter, Streptomyces, Stenotrophomonas and Pseudomonas, more preferably one selected from the group consisting of Escherichia coli, Klebsiella planticola, Bacillus licheniformis, Bacillus lentus, Bacillus amyloliquefaciens, Bacillus subtilis, Bacillus alcalophilus, Bacillus globigii, Bacillus gibsonii, Bacillus clausii, Bacillus halodurans, Bacillus pumilus, Staphylococcus carnosus, Corynebacterium glutamicum , Arthrobacter oxidans, Streptomyces lividans, Streptomyces coelicolor and Stenotrophomonas maltophilia.

The host cell may also be a eukaryotic cell, which is characterized by having a cell nucleus. A further subject of the invention therefore represents a host cell, which is characterized in that it has a cell nucleus. In contrast to prokaryotic cells, eukaryotic cells are capable of post-translationally modifying the protein formed. Examples thereof are fungi such as Actinomycetes or yeasts such as Saccharomyces or Kluyveromyces.

This may be particularly advantageous, for example, if the proteins are to undergo specific modifications in the context of their synthesis that enable such systems. Among the modifications that eukaryotic systems perform, particularly in the context of protein synthesis, include, for example, the binding of low molecular weight compounds such as membrane anchors or Oligosaccharides. Such oligosaccharide modifications may be desirable, for example, to lower the allergenicity of an expressed protein. Also co-expression with the enzymes naturally produced by such cells, such as cellulases, may be advantageous. Furthermore, for example, thermophilic fungal expression systems may be particularly suitable for the expression of temperature-resistant proteins or variants. In preferred embodiments of the invention, the host cell is a basidiomycete cell.

The host cells according to the invention are cultured and fermented in the usual way, for example in discontinuous or continuous systems. In the first case, a suitable nutrient medium is inoculated with the host cells and the product is harvested from the medium after an experimentally determined period of time. Continuous fermentations are characterized by achieving a flow equilibrium, in which over a relatively long period of time cells partly die out but also regrow and at the same time the protein formed can be removed from the medium.

1. a) Kultivieren einer erfindungsgemäßen Wirtszelle, und
2. b) Isolieren der Amylase aus dem Kulturmedium oder aus der Wirtszelle.

Host cells according to the invention are preferably used to produce amylases according to the invention. Another object of the invention is therefore a process for preparing an amylase comprising

1. a) cultivating a host cell according to the invention, and
2. b) isolating the amylase from the culture medium or from the host cell.

This subject invention preferably comprises fermentation processes. Fermentation processes are known per se from the prior art and represent the actual large-scale production step, usually followed by a suitable purification method of the product produced, for example the amylase according to the invention. All fermentation processes which are based on a corresponding process for preparing an amylase according to the invention represent embodiments of this subject matter of the invention.

Fermentation processes, which are characterized in that the fermentation is carried out via a feed strategy, come in particular into consideration. Here, the media components consumed by the ongoing cultivation are fed. As a result, considerable increases can be achieved both in the cell density and in the cell mass or dry mass and / or in particular in the activity of the amylase of interest.

Furthermore, the fermentation can also be designed so that undesired metabolic products are filtered out or neutralized by the addition of buffer or suitable counterions.

The produced amylase can be harvested from the fermentation medium. Such a fermentation process is resistant to isolation of the amylase from the host cell, i. however, requires the provision of suitable host cells or one or more suitable secretion markers or mechanisms and / or transport systems for the host cells to secrete the amylase into the fermentation medium. Alternatively, without secretion, isolation of the amylase from the host cell, i. a purification of the same from the cell mass, carried out, for example by precipitation with ammonium sulfate or ethanol, or by chromatographic purification.

All of the above-described facts can be combined into processes to produce amylases of the invention.

Another object of the invention is an agent characterized by containing an amylase as described herein. The amylase has 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85 %, 86%, 87%, 88%, 89%, 90%, 90.5%, 91%, 91.5%, 92%, 92.5%, 93%, 93.5%, 94%, 94 , 5%, 95%, 95.5%, 96%, 96.5%, 97%, 97.5%, 98%, 98.5%, 98.6%, 98.7%, 98.8% , 98.9%, 99.0%, 99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8% or 99.9% sequence identity with the sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2, or is a variant thereof as described above, which is obtainable starting from an above-described amylase as the starting molecule and before and preferably also after the variation, the specified sequence identity with SEQ ID NO. 1 or SEQ ID NO. 2 has. The agent is preferably a washing or cleaning agent.

This invention includes all conceivable types of detergents or cleaners, both concentrates and undiluted agents, for use on a commercial scale, in the washing machine or in hand washing or cleaning. These include detergents for textiles, carpets, or natural fibers, for which the term detergent is used. These include, for example, dishwashing detergents for dishwashers or manual dishwashing detergents or cleaners for hard surfaces such as metal, glass, porcelain, ceramics, tiles, stone, painted surfaces, plastics, wood or leather, for which the term detergent is used, ie in addition to manual and machine Dishwashing agents, for example, scouring agents, glass cleaner, toilet scenters, etc. The washing and cleaning agents in the invention also include laundry aids, which are added to the actual detergent in the manual or machine textile laundry to achieve a further effect. Furthermore, laundry detergents and cleaners in the context of the invention also include textile pre-treatment and post-treatment agents, ie those agents with which the laundry item is brought into contact before the actual laundry, for example to dissolve stubborn soiling, and also agents which are in one of the actual Textile laundry downstream step to give the laundry further desirable properties such as comfortable grip, crease resistance or low static charge. Amongst others, the fabric softeners are calculated.

The washing or cleaning agents according to the invention, which may be in the form of homogeneous solutions or suspensions in the form of powdered solids, may contain, in addition to an amylase according to the invention, all known ingredients customary in such agents, preferably containing at least one further ingredient in the composition , The agents according to the invention may in particular contain surfactants, builders, peroxygen compounds or bleach activators. In addition, they may contain water-miscible organic solvents, further enzymes, sequestering agents, electrolytes, pH regulators and / or further auxiliaries such as optical brighteners, grayness inhibitors, foam regulators, as well as dyes and fragrances, and combinations thereof.

In particular, a combination of an amylase according to the invention with one or more further ingredients of the composition is advantageous, since in preferred embodiments according to the invention such an agent has an improved cleaning performance by virtue of resulting synergisms. In particular, by combining an amylase according to the invention with a surfactant and / or a builder (builder) and / or a peroxygen compound and / or a bleach activator, such a synergism can be achieved.

Advantageous ingredients of agents according to the invention are disclosed in the international patent application WO 2009/121725 starting there on page 5, penultimate paragraph, and ending on page 13 after the second paragraph. This disclosure is incorporated herein by reference and the disclosure is incorporated herein by reference.

1. (a) 1 bis 85 Gew.-%, vorzugsweise 5 bis 65 Gew.-%, Tenside enthält; und/oder
2. (b) 0 bis 45 Gew.-%, vorzugsweise 0,1 bis 15 Gew.-%, Builder (Gerüststoffe) enthält; und/oder
3. (c) 0,0005 bis 15 Gew.-%, vorzugsweise 0,001 bis 5 Gew.-%, Protease enthält; und/oder
4. (d) 0,0005 bis 15 Gew.-%, vorzugsweise 0,001 bis 5 Gew.-%, Lipase enthält; und/oder
5. (e) 0,00005 bis 15 Gew.-%, vorzugsweise 0,0001 bis 5 Gew.-%, Mannanase enthält; und/oder
6. (f) 0,00005 bis 15 Gew.-%, vorzugsweise 0,0001 bis 5 Gew.-%, Cellulase/Pektatlyase enthält; und/oder
7. (g) 0,00005 bis 15 g/Waschladung, vorzugsweise 0,0001 bis 5 g/Waschladung, Xanthanlyase enthält; und/oder
8. (h) 0,00005 bis 15 g/Waschladung, vorzugsweise 0,00005 bis 15 g/Waschladung, Endoglucanase, die fähig ist Xanthan zu verdauen, enthält.

In further embodiments of the invention, the agent is characterized in that it

1. (A) 1 to 85 wt .-%, preferably 5 to 65 wt .-%, surfactants; and or
2. (b) 0 to 45 wt .-%, preferably 0.1 to 15 wt .-% builder (builders); and or
3. (c) 0.0005 to 15 wt%, preferably 0.001 to 5 wt%, of protease; and or
4. (d) 0.0005 to 15% by weight, preferably 0.001 to 5% by weight, of lipase; and or
5. (e) 0.00005 to 15% by weight, preferably 0.0001 to 5% by weight, of mannanase; and or
6. (f) 0.00005 to 15% by weight, preferably 0.0001 to 5% by weight, of cellulase / pectate lyase; and or
7. (g) 0.00005 to 15 g / wash load, preferably 0.0001 to 5 g / wash load, xanthan lyase; and or
8. (h) 0.00005 to 15 g / wash load, preferably 0.00005 to 15 g / wash load, endoglucanase capable of digesting xanthan gum.

An agent of the invention advantageously contains the amylase in an amount of from 2 μg to 20 mg, preferably from 5 μg to 17.5 mg, more preferably from 20 μg to 15 mg and most preferably from 50 μg to 10 mg per gram of the agent. In addition, the agent according to the invention may advantageously contain the amylase in an amount of from 0.00005 to 15% by weight, based on the active enzyme and the total weight of the composition, preferably from 0.0001 to 5% by weight and more preferably from 0.001 to 1 wt .-% included. Further, the amylase contained in the agent, and / or other ingredients of the agent, with a substance impermeable to the enzyme at room temperature or in the absence of water, which becomes permeable to the enzyme under conditions of use of the agent. Such an embodiment of the invention is thus characterized in that the amylase is coated with a substance which is impermeable to the amylase at room temperature or in the absence of water. Furthermore, the washing or cleaning agent itself may be packaged in a container, preferably an air-permeable container, from which it is released shortly before use or during the washing process.

1. a) in fester Form vorliegt, insbesondere als rieselfähiges Pulver mit einem Schüttgewicht von 300 g/l bis 1200 g/l, insbesondere 500 g/l bis 900 g/l, oder
2. b) in pastöser oder in flüssiger Form vorliegt, und/oder
3. c) in gelförmiger oder dosierbeutelförmiger (Pouches) Form vorliegt, und/oder
4. d) als Einkomponentensystem vorliegt, oder
5. e) in mehrere Komponenten aufgeteilt ist.

In further embodiments of the invention, the agent is characterized in that it

1. a) is in solid form, in particular as a free-flowing powder having a bulk density of 300 g / l to 1200 g / l, in particular 500 g / l to 900 g / l, or
2. b) is present in pasty or in liquid form, and / or
3. c) is in a gel or Dosierbeutelelförmiger (pouches) form, and / or
4. d) is present as a one-component system, or
5. e) is divided into several components.

These embodiments of the present invention include all solid, powdered, liquid, gelatinous or paste-like administration forms of compositions according to the invention, which if appropriate can also consist of several phases and can be present in compressed or uncompressed form. The agent can be present as a free-flowing powder, in particular with a bulk density of 300 g / l to 1200 g / l, in particular 500 g / l to 900 g / l or 600 g / l to 850 g / l. The solid dosage forms of the composition also include extrudates, granules, tablets or pouches. Alternatively, the agent can also be liquid, gelatinous or pasty, for example in the form of a non-aqueous liquid detergent or a non-aqueous paste or in the form of an aqueous liquid detergent or a water-containing paste. Furthermore, the agent may be present as a one-component system. Such funds consist of one phase.

Alternatively, an agent can also consist of several phases. Such an agent is therefore divided into several components.

Detergents or cleaning agents according to the invention may contain exclusively an amylase. Alternatively, they may also contain other hydrolytic enzymes or other enzymes in a concentration effective for the effectiveness of the agent. A further embodiment of the invention thus represents agents which further comprise one or more further enzymes. Preferred enzymes which can be used as enzymes are all enzymes which can display catalytic activity in the composition according to the invention, in particular a protease, lipase, cellulase, hemicellulase, mannanase, tannase, xylanase, xanthanase, xyloglucanase, β-glucosidase, pectinase, carrageenase, perhydrolase, Oxidase, oxidoreductase or other - distinguishable from the amylases of the invention - amylases, and mixtures thereof. Additional enzymes are advantageously included in the agent each in an amount of 1 × 10 ^-8 to 5% by weight based on active protein. More preferably, each further enzyme is in an amount of 1 x 10 ^-7 to 3 wt%, from 0.00001 to 1 wt%, from 0.00005 to 0.5 wt%, of 0.0001 to 0.1 wt .-% and particularly preferably from 0.0001 to 0.05 wt .-% in inventive compositions, based on active protein. Particularly preferably, the enzymes show synergistic cleaning performance against certain stains or stains, ie the enzymes contained in the middle composition mutually support each other in their cleaning performance. Very particular preference is given to such a synergism between the amylase according to the invention and another enzyme of an agent according to the invention, including in particular between said amylase and a lipase and / or a protease and / or a mannanase and / or a cellulase and / or a pectinase , Synergistic effects can occur not only between different enzymes, but also between one or more enzymes and other ingredients of the composition according to the invention.

In the cleaning agents described herein, the enzymes to be used may also be formulated together with accompanying substances, for example from the fermentation. In liquid formulations, the enzymes are preferably used as enzyme liquid formulation (s).

The enzymes are usually not provided in the form of the pure protein, but rather in the form of stabilized, storable and transportable preparations. Such prefabricated preparations include, for example, the solid preparations obtained by granulation, extrusion or lyophilization or, in particular in the case of liquid or gel-form detergents, solutions of the enzymes, advantageously as concentrated as possible, sparing in water and / or mixed with stabilizers or further auxiliaries.

Alternatively, the enzymes may be encapsulated for both the solid and liquid dosage forms, for example by spray-drying or extruding the enzyme solution together with a preferably natural polymer or in the form of capsules, for example those in which the enzymes are entrapped as in a solidified gel or in those of the core-shell type, in which an enzyme-containing core is coated with a water, air and / or chemical impermeable protective layer. In deposited layers, further active ingredients, for example stabilizers, emulsifiers, pigments, bleaches or dyes, may additionally be applied. Such capsules are applied by methods known per se, for example by shaking or rolling granulation or in fluid-bed processes. Advantageously, such granules, for example by applying polymeric film-forming agent, low in dust and storage stable due to the coating.

The enzymes can also be incorporated into water-soluble films. Such a film allows the release of the enzymes after contact with water. As used herein, "water-soluble" refers to a film structure that is preferably completely water-soluble. However, even films that are substantially water-soluble but have relatively small amounts of a material in the film structure that is not water-soluble; Films containing materials which are water-soluble only at relatively high water temperatures or only under limited pH conditions; and films including a relatively thin layer of water-insoluble material, all included in the term "water-soluble". Preferably, such a film consists of (fully or partially hydrolyzed) polyvinyl alcohol (PVA). However, the film may also contain, solely or in addition to the PVA, acid / acrylate copolymers, preferably methacrylic acid / ethyl acrylate copolymer such as that available from Belland as GBC 2580 and 2600; Styrene-maleic anhydride copolymer (SMA) (available as Scripset (trade name) from Monsanto); Ethylene-acrylic acid copolymer (EAA) or metal salt neutralized ethylene-methacrylic acid copolymer (EMAA), known as ionomer (available from DuPont), wherein the acid content of EAA or EMAA is at least about 20 mole%; Polyether block copolymer; Polyhydroxyvaleric acid (available as Biopol (trade name) resins from Imperial Chemical Industries); polyethylene oxide; water-soluble polyester or copolyester; Polyethyloxazoline (PEOX 200 from Dow); and water-soluble polyurethane.

Furthermore, it is possible to assemble two or more enzymes together so that a single granule has several enzyme activities.

A further subject of the invention is a process for the cleaning of textiles or hard surfaces, which is characterized in that in at least one process step, an inventive agent is applied, or that in at least one process step, an amylase of the invention is catalytically active, in particular such that the amylase in an amount of from 40 μg to 4 g, preferably from 50 μg to 3 g, more preferably from 100 μg to 2 g and most preferably from 200 μg to 1 g is used.

In various embodiments, the method described above is characterized in that the amylase at a temperature of 0 to 100 ° C, preferably from 0 to 60 ° C, more preferably from 20 to 45 ° C and most preferably used at 40 ° C. becomes.

These include both manual and mechanical processes, with mechanical processes being preferred. Methods for cleaning textiles are generally distinguished by the fact that various cleaning-active substances are applied to the items to be cleaned and washed off after the contact time, or that the items to be cleaned are otherwise treated with a detergent or a solution or dilution of this product. The same applies to processes for cleaning all other materials than textiles, especially hard surfaces. All conceivable washing or cleaning processes can be enriched in at least one of the process steps by the use of a washing or cleaning agent or an amylase according to the invention and then represent embodiments of the present invention. All facts, objects and embodiments which are essential for amylases according to the invention and those containing them Means are described are also applicable to this subject invention. Therefore, reference is made at this point expressly to the disclosure in the appropriate place with the statement that this disclosure also applies to the above inventive method.

Since amylases according to the invention naturally already have a hydrolytic activity and also unfold them in media which otherwise have no cleaning power, as for example in bare buffer, a single and / or the sole step of such a method can consist in the fact that, if desired, the only cleaning-active component is an inventive Amylase is brought into contact with the soiling, preferably in a buffer solution or in water. This represents a further embodiment of this subject of the invention.

Alternative embodiments of this subject matter of the invention are also processes for the treatment of textile raw materials or for textile care, in which an amylase according to the invention becomes active in at least one process step. Among these, methods for textile raw materials, fibers or textiles with natural components are preferred, and especially for those with wool or silk.

In a further aspect, the present invention relates to the use of an amylase according to the invention or an amylase obtainable by a process according to the invention in a washing or cleaning agent for removing starch-containing stains.

All aspects, objects, and embodiments described for amylase and agents containing it are also applicable to the described methods and uses. Therefore, reference is made at this point expressly to the disclosure in the appropriate place with the statement that this disclosure also applies to the above uses and methods according to the invention.

In a further aspect, the present invention relates to the use of an amylase according to the invention or an amylase obtainable by a process according to the invention or an amylase as used in the agents of the invention in a washing or cleaning agent for removing starch-containing stains. All aspects, objects and embodiments described for amylase and agents containing it are also applicable to this subject of the invention.

Examples

Example 1: Identification of the amylase

It was screened in Basidiomycetes for starch degrading enzymes. A wild-type enzyme, annotated as alpha-amylase, was discovered from Fomes fomentarius (Ffo). This amylase showed good washing performance on various starchy textiles.

The sequence of the amylase found in Fomes fomentarius differs significantly from the sequences of amylases previously used in detergents and cleaners. This opens up many possibilities for increasing the genetic and biochemical diversity in the field of amylases used in cleaning agents.

Example 2: Screening for Amylase with Washing Performance

Cultivation and concentration

All basidiomycetes were cultured in a standard liquid nutrient (SNL) medium, replacing glucose with 1% soluble starch as the carbon source. The presence of starch in the medium was checked by Lugol's solution. To this was added 20 μl of Lugol's solution (Sigma) to 200 μl of culture supernatant. If no more starch was detectable in the medium, the cultivation was stopped. After culturing for six days, the culture supernatant to increase the enzyme concentration was concentrated using Centricons® Plus 70 membranes (Merck Milipore, Darmstadt, MWCO 10 kDa). The centrifugation, which was carried out at 3500 g and 4 ° C, was stopped as soon as the liquid flow had stopped.

The separation of the unknown glycoside hydrolases from the concentrated culture supernatants was achieved by ion exchange chromatography. Due to the generally acidic plc of the glycoside hydrolases, strong (1 ml QXL) and weak (1 ml DEAE) anion exchange materials were used for purification (GE Healthcare, Chalfont St Gilles, GBR).

Example 3: Activity assay for amylase

For the determination of the amylolytic activity of amylases of the invention, a modified para-nitrophenyl maltoheptaoside was used whose terminal glucose unit was blocked by a benzylidene group. From this molecule is released by the amylase para-nitrophenyl oligosaccharide, which in turn is converted by the enzymes glucoamylase and alpha-glucosidase to glucose and para-nitrophenol. Thus, the amount of released para-nitrophenol is proportional to the activity of the amylase. The measurement is carried out, for example, using the Quick-Start® test kit from Abbott (Abbott Park, Illinois, USA). The increase in absorbance (405 nm) in the test mixture was determined at 37 ° C. for 3 minutes compared to a photometric control value (blank value). Calibration was performed on an enzyme standard of known activity (e.g., Maxamyl® / Purastar® 2900 Genencor 2900 TAU / g). The evaluation was carried out by determining the absorption difference dE (405 nm) per minute against the enzyme concentration of the standard.

Example 4: Washing test and results

A washing test was carried out with the purified wild-type supernatant from Fomes fomentarius, in which the described amylase is present.

Conditions: 40 ° C, 16 ° dH water, 1 h;

Enzyme concentration: 0.186 TAU / ml (determination of amylase activity with benzylidene-blocked para-nitrophenol-maltoheptaoside); this corresponds to the amount of amylase usually used in detergents.

stains: 1. CS-27 Potato starch (from CFT) Second CS-26 Corn starch (from CFT)

• Execution:
  • - Place punched tissue (diameter = 10 mm) in microtiter plate, preheat the wash liquor to 40 ° C, final concentration 4.58 g / L;
  • - Add lye and enzyme to the stain, incubate for 1 h at 40 ° C and 600 rpm;
  • - Then rinse the soiling several times with clean water, leave to dry and determine the brightness with a colorimeter.

The lighter the tissue, the better the cleaning performance. Measured here is the L value = brightness, the higher the brighter.

• Probe 1: nur Waschmittel als Benchmark (Vergleichsreferenz)
• Probe 2: Waschmittel plus Amylase aus Fomes fomentarius (gemäß SEQ ID NO. 1)

It is washed with a common liquid detergent without enzymes (see Table 2).

• Sample 1: only detergent as benchmark (comparison reference)
• Sample 2: detergent plus amylase from Fomes fomentarius (according to SEQ ID NO. 1)

The results are shown in Table 1. Table 1: Results of the washing tests soiling Sample 1 Sample 2 potato starch 75.0 77.5 corn starch 75.9 78.5

It is clear that the amylase on both soils causes improved performance of the detergent. As a negative control, the boiled, purified supernatant from Fomes fomentarius (99 ° C for 30 min) was washed with it, which shows no washing performance (not shown). Table 2: Used detergent matrix Chemical name Wt .-% active substance in the raw material Wt .-% active ingredient in the formulation Water demin. 100 rest alkyl benzene sulfonic acid 96 4.40 Other anionic surfactants 70 5.60 C ₁₂ -C ₁₈ fatty acids Na salt 30 2.40 Nonionic surfactants 100 4.40 phosphonates 40 0.20 citric acid 100 1.40 NaOH 50 0.95 defoamers tq 0.01 glycerin 100 2.00 preservative 100 0.08 ethanol 93 1.00

The matrix used contained no optical brighteners, perfumes, dyes or enzymes. Dosage: 4.58 g / L

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited patent literature

• US 8512986 [0003]
• US 7407677 B2 [0003]
• US 8852912 B2 [0003]
• WO 2009/121725 [0076]

Cited non-patent literature

• Altschul, S.F., Gish, W., Miller, W., Myers, E.W. & Lipman, D.J. (1990): "Basic local alignment search tool", J. Mol. Biol. 215: 403-410 [0018]
• Altschul, Stephan F., Thomas L. Madden, Alejandro A. Schaffer, Jinghui Zhang, Hheng Zhang, Webb Miller, and David J. Lipman (1997): "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs Nucleic Acids Res. 25: 3389-3402 [0018]
• Chenna et al. (2003): "Multiple sequence alignment with the Clustal series of programs", Nucleic Acid Res. 31: 3497-3500 [0018]
• Notredame et al. (2000): "T-Coffee: A novel method for multiple sequence alignments", J. Mol. Biol. 302: 205-217 [0018]
• Gornall, C.S. Bardawill and M.M. David, J. Biol. Chem., 177 (1948), pp. 751-766 [0027]
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• Sambrook, J., Fritsch, E.F. and Maniatis, T. 2001. Molecular cloning: a laboratory manual, 3rd Edition Cold Spring Laboratory Press [0053]

Claims (11)

An amylase comprising an amino acid sequence which has at least 70% sequence identity with the amino acid sequence shown in SEQ ID NO. 1 or SEQ ID NO. 2 has indicated amino acid sequence over the entire length. Amylase or variants thereof, wherein these variants are characterized in that a) they from an amylase according to Claim 1 are obtainable as starting molecule by one or more conservative amino acid substitution; and / or b) from an amylase Claim 1 can be obtained as a starting molecule by fragmentation, deletion, insertion or substitution mutagenesis and an amino acid sequence over a length of at least 396, 400, 410, 420, 430, 440, 450, 460, 470, 480, 490, 500, 510 , 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566, or 567 contiguous amino acids matches the parent molecule. A method for producing an amylase according to Claim 1 or 2 comprising providing a parent amylase having at least 70% sequence identity to that shown in SEQ ID NO. 1 or SEQ ID NO. 2 has indicated amino acid sequence over the entire length. Method according to Claim 3 further comprising one or both of the following method steps: a) introducing a single or multiple conservative amino acid substitution into the parent amylase; b) altering the amino acid sequence of the parent amylase by fragmentation, deletion, insertion or substitution mutagenesis such that the altered amylase comprises an amino acid sequence of at least 396, 400, 410, 420, 430, 440, 450, 460 , 470, 480, 490, 500, 510, 520, 530, 540, 550, 555, 556, 557, 558, 559, 560, 561, 562, 563, 564, 565, 566 or 567 contiguous amino acids with the starting Amylase matches. Nucleic acid coding for an amylase after Claim 1 or 2 or coding for one according to a method Claim 3 or 4 obtained amylase. Vector containing a nucleic acid according to Claim 5 , in particular a cloning vector or an expression vector. Non-human host cell that replaces a nucleic acid Claim 5 or a vector after Claim 6 contains, or the an amylase after Claim 1 or 2 includes, or the one according to a method Claim 3 or 4 containing amylase, especially one which secretes the amylase into the medium surrounding the host cell. A process for producing an amylase comprising a) cultivating a host cell according to Claim 7 ; and b) isolating the amylase from the culture medium or from the host cell. Agent, in particular a detergent or cleaning agent, characterized in that it contains at least one amylase Claim 1 or 2 or one after a procedure Claim 3 or 4 containing amylase, wherein the amylase in particular in an amount of 0.00005 to 15 wt .-%, preferably from 0.0001 to 5 wt .-% and particularly preferably from 0.001 to 1 wt .-% based on active protein in the Means is included. Process for the cleaning of textiles or hard surfaces, characterized in that in at least one process step, an agent Claim 9 is applied, or that in at least one process step, an amylase after Claim 1 or 2 or one after a procedure Claim 3 or 4 obtained amylase is catalytically active. Use of an amylase after Claim 1 or 2 or one after a procedure Claim 3 or 4 obtained amylase in a washing or cleaning agent to remove starchy stains.