摘要:
The present application relates to two novel alkaline proteases (SEQ ID NO. 4 and 7) which are similar to one another, whose DNA was obtained from soil samples, and C-terminally deleted, likewise proteolytically active fragments thereof (SEQ ID NO. 5 and 8), all alkaline proteases similar at least to 90% to SEQ ID NO. 4 or to 87.5% to SEQ ID NO. 7, and those which can be summarized under a consensus sequence (SEQ ID NO. 9) derived from SEQ ID NO. 4 and 7. Furthermore it relates to all nucleic acids which have a homology of at least 85% identity to the associated nucleic acids (SEQ ID NO. 3 and 6) or the fragments concerned. Furthermore, it defines technical possibilities of use for these proteases and especially describes their use in detergents and cleaners.
摘要翻译:本申请涉及两个彼此相似的碱性蛋白酶(SEQ ID NO.4和7),其DNA是从土壤样品获得的,并且C末端缺失,同样蛋白水解活性片段(SEQ ID NO.5 和8),所有碱性蛋白酶类似于至少90%的SEQ ID NO。 4或至87.5%。 7,以及可以在源自SEQ ID NO:1的共有序列(SEQ ID NO.9)中总结的那些。 此外,它涉及与相关核酸(SEQ ID NO.3和6)或相关片段具有至少85%同一性的同源性的所有核酸。 此外,它定义了用于这些蛋白酶的技术可能性,特别描述了它们在洗涤剂和清洁剂中的应用。
摘要:
The invention relates to a novel alkaline protease, the DNA thereof having been taken from a bottom sample, to all alkaline proteases that are at least 40% identical, and to all nucleic acids with an identity at least 50% homologous with the associated nucleic acids. The invention also relates to the fragment of said protease, comprising the amino acid positions 108 to 325, in addition to the gene fragment coding therefor, and to all alkaline proteases that are at least 60% identical, or nucleic acids that are at least 70% identical. Furthermore, the invention defines technical possibilities of use for said proteases and especially describes the use thereof in washing and cleaning products.
摘要:
The present application relates to two novel proteases (SEQ ID NO: 4 and 7) which are similar to one another. The DNA of the two proteases, was obtained from soil samples, and C-terminally deleted, producing proteolytically active fragments thereof (SEQ ID NO: 5 and 8). The invention also provides all alkaline proteases similar at least to 90% to SEQ ID NO: 4 or to 87.5% to SEQ ID NO: 7, and those which can be summarized under a consensus sequence (SEQ ID NO: 9) derived from SEQ ID NO: 4 and 7. Furthermore, it relates to all nucleic acids which have a homology of at least 85% identity to the associated nucleic acids (SEQ ID NO: 3 and 6) or the fragments concerned. Furthermore, it defines technical possibilities of use for these proteases and especially describes their use in detergents and cleaners.
摘要翻译:本申请涉及两个彼此相似的新型蛋白酶(SEQ ID NO:4和7)。 两种蛋白酶的DNA从土壤样品获得,并且C末端缺失,产生其蛋白水解活性片段(SEQ ID NO:5和8)。 本发明还提供了类似于SEQ ID NO:4至少90%或SEQ ID NO:7至87.5%的所有碱性蛋白酶,以及可归纳于SEQ ID NO:7衍生的共有序列(SEQ ID NO:9) 此外,它涉及与相关核酸(SEQ ID NO:3和6)或相关片段具有至少85%同一性的同源性的所有核酸。 此外,它定义了用于这些蛋白酶的技术可能性,特别描述了它们在洗涤剂和清洁剂中的应用。
摘要:
The present application relates to two novel proteases (SEQ ID NO: 4 and 7) which are similar to one another, whose DNA was obtained from soil samples, and C-terminally deleted, likewise proteolytically active fragments thereof (SEQ ID NO: 5 and 8), all alkaline proteases similar at least to 90% to SEQ ID NO: 4 or to 87.5% to SEQ ID NO: 7, and those which can be summarized under a consensus sequence (SEQ ID NO: 9) derived from SEQ ID NO: 4 and 7. Furthermore, it relates to all nucleic acids which have a homology of at least 85% identity to the associated nucleic acids (SEQ ID NO: 3 and 6) or the fragments concerned. Furthermore, it defines technical possibilities of use for these proteases and especially describes their use in detergents and cleaners.
摘要翻译:本申请涉及两个彼此相似的新型蛋白酶(SEQ ID NO:4和7),其DNA从土壤样品获得,并且C末端缺失,同样蛋白水解活性片段(SEQ ID NO:5和 8),所有与SEQ ID NO:4至少90%相同的碱性蛋白酶或与SEQ ID NO:7相似至87.5%的那些,以及源自SEQ ID NO:7的共有序列(SEQ ID NO:9) 此外,它涉及与相关核酸(SEQ ID NO:3和6)或相关片段具有至少85%同一性的同源性的所有核酸。 此外,它定义了用于这些蛋白酶的技术可能性,特别描述了它们在洗涤剂和清洁剂中的应用。
摘要:
An alkaline protease, the DNA thereof having been taken from a bottom sample, alkaline proteases that are at least 40% identical, and nucleic acids with an identity at least 50% homologous with the associated nucleic acids. The invention also relates to the fragment of said protease comprising the amino acid positions 108 to 325, in addition to the gene fragment coding therefor, and alkaline proteases that are at least 60% identical or nucleic acids that are at least 70% identical. Furthermore, the invention defines technical possibilities of use for said proteases, especially use thereof in washing and cleaning products.
摘要:
The present application relates to two novel alkaline proteases (SEQ ID NO. 4 and 7) which are similar to one another, whose DNA was obtained from soil samples, and which were C-terminally deleted. The present application also provides proteolytically active fragments thereof (SEQ ID NO. 5 and 8), all alkaline proteases similar at least to 90% to SEQ ID NO. 4 or to 87.5% to SEQ ID NO. 7, and those which can be summarized under a consensus sequence (SEQ ID NO. 9) derived from SEQ ID NO. 4 and 7. Furthermore, the present application relates to all nucleic acids which have a homology of at least 85% identity to the associated nucleic acids (SEQ ID NO. 3 and 6) or the fragments concerned. Furthermore, the present application relates to use for these proteases and especially describes their use in detergents and cleaners.
摘要翻译:本申请涉及两种彼此相似的新型碱性蛋白酶(SEQ ID NO.4和7),其DNA从土壤样品中获得,并且被C末端缺失。 本申请还提供了其蛋白水解活性片段(SEQ ID NO.5和8),所有碱性蛋白酶类似于SEQ ID NO.1至少90%。 4或至87.5%。 7,以及可以在源自SEQ ID NO:1的共有序列(SEQ ID NO.9)中总结的那些。 此外,本申请涉及与相关核酸(SEQ ID NO.3和6)或相关片段具有至少85%同一性的同源性的所有核酸。 此外,本申请涉及这些蛋白酶的用途,特别描述了它们在洗涤剂和清洁剂中的用途。
摘要:
The invention relates to a new glycosyl hydrolases with an amyloltic activity and nucleic acids coding for said gylcosyl hydrolases, A PCR-based method for identifying and preparing new gylcosyl hydrolases from metagenome DNA and several possible technical uses for such glycosyl hydrolases with an amylolytic activity. Washing and cleaning products containing such enzymes, and methods and possible uses corresponding thereto are particularly interesting.
摘要:
The invention relates to a new glycosyl hydrolases with an amyloltic activity and nucleic acids coding for said gylcosyl hydrolases, A PCR-based method for identifying and preparing new gylcosyl hydrolases from metagenome DNA and several possible technical uses for such glycosyl hydrolases with an amylolytic activity. Washing and cleaning products containing such enzymes, and methods and possible uses corresponding thereto are particularly interesting.
摘要:
The invention relates to a DNA sequence, which codes for a polypeptide having phospholipase activity essentially without lipase activity, characterized in that the DNA sequence is selected from a) DNA sequences that comprise a nucleotide sequence according to SEQ ID NO: 1, b) DNA sequences that comprise the coding sequence according to SEQ ID NO: 1, c) DNA sequences that code for the protein sequence according to SEQ ID NO: 2, d) DNA sequences that are coded for by the plasmid pPL3940-Topo2.5 with the restriction map according to FIG. 7, which is deposited under accession number DSM 22741, e) DNA sequences that hybridize under stringent conditions with one of the DNA sequences according to a), b), c) or d), f) DNA sequences that are related to the DNA sequences according to a), b), c), d) or e) due to the degeneration of the genetic code, and g) complementary strands to the sequences according to a) to f), wherein the DNA sequence is preferably derived from Aspergillus, and more preferably from Aspergillus fumigatus, and a polypeptide having phospholipase activity essentially without lipase activity selected from a) a polypeptide which is coded for by the coding part of a DNA sequence as defined above, b) a polypeptide having the sequence according to SEQ ID NO: 2 or a sequence derived therefrom, which may be obtained by substitution, addition, deletion of one or more amino acid(s), c) a polypeptide having a sequence that has at least 83% identity with the amino acids 1 to 299 of SEQ ID NO: 2, d) a polypeptide which is coded for by a nucleic acid sequence which hybridizes under stringent conditions with (i) nucleotides 55 to 1106 of SEQ ID NO: 1, (ii) the cDNA sequence contained in nucleotides 55 to 1106 of SEQ ID NO: 1, (iii) a partial sequence of (i) or (ii) composed of at least 100 nucleotides, or (iv) a complementary strand of (i), (ii) or (iii), e) a variant of the polypeptide having SEQ ID NO: 2, comprising a substitution, deletion and/or insertion of one or more amino acid(s), f) allelic variants to amino acid sequences a) to e).
摘要:
The invention relates to novel polypeptides which have the biological activity of an NAD- or NADP-dependent alcohol dehydrogenase. The invention furthermore relates to nucleic acids encoding said polypeptides, to nonhuman hosts or host cells and to reaction systems which may be used for preparing desired products. The polypeptides of the invention are preferably used in the preparation, starting from aldehydes or ketones, of primary and enantiomerically pure secondary alcohols which may serve as intermediates for medicaments. Alternatively, the polypeptides of the invention may also be employed in the reverse reaction, i.e. the oxidation of alcohols with the formation of aldehydes or ketones.