摘要:
An enzyme exhibiting xylanase activity, which enzyme is immunologically reactive with an antibody raised against a purified xylanase derived from Aspercgillus aculeatus, CBS 101.43. The enzyme may be used for degrading plant cell wall components, e.g., in the preparation of feed, in baking, in the paper and pulp industry and in connection with separation of wheat into starch and gluten.
摘要:
A desired protein having the formula:A-B-C-Pwhereina) A is Lys or Arg, and B and C are arbitrary amino acids, orb) A is an arbitrary amino acid different from Pro, Lys and Arg, and B and/or C is Pro,is produced from a biosynthetically formed amino acid extended protein having the formula:X-A-B-C-Pwherein A, B, C and P are as defined above, and X is an amino acid sequence with an even number of amino acids, of which the first one, seen from the N-terminal end, is different from Lys and Arg, all other uneven amino acids are different from Pro, Lys and Arg, and all even amino acids are different from Pro, by reaction with the enzyme dipeptidyl aminopeptidase (DAP I). The desired protein is obtained in a pure state. Thus, e.g. hGH without content of Met-hGH may be produced by the process.
摘要:
The present invention relates to methods for producing heterologous heme proteins extracellularly comprising transforming a filamentous fungus with a vector comprising a DNA sequence encoding the heterologous heme protein and a DNA sequence encoding a preregion permitting secretion of the expressed heme protein, and culturing the transformed filamentous fungus in a suitable culture medium to produce the heme protein.
摘要:
The present invention relates to DNA sequences encoding a rhamnogalacturonase which comprises(a) the DNA sequence of nucleotides 64-1587 of SEQ ID NO:1;(b) a DNA sequence which hybridizes to the same probe as nucleotides 64-1587 of SEQ ID NO:1 under conditions of presoaking in 5.times.SSC and prehybridizing for 1 hour at -40.degree. C. in a solution of 5.times.SSC, 5.times.Denhardt's solution, 50 mM sodium phosphate, pH 6.8, and 50 mg of denatured sonicated calf thymus DNA, followed by hybridization in the same solution supplemented with 50 .mu.Ci 32-P-dCTP labelled probe for 18 h at -40.degree. C., followed by washing three times in 2.times.SSC, 0.2% SDS at 40.degree. C. for 30 minutes; or(c) a DNA sequence encoding an amino acid sequence having amino acids 20-527 of the sequence of SEQ ID NO;2.
摘要翻译:本发明涉及编码鼠李糖半乳糖醛酸酶的DNA序列,其包含(a)SEQ ID NO:1的核苷酸64-1587的DNA序列; (b)在5×SSC中预浸泡的条件下,在-40℃下在5×SSC,5×丹登溶液50μl的溶液中预杂交1小时,与SEQ ID NO:1的核苷酸64-1587相同的探针杂交的DNA序列 mM磷酸钠,pH 6.8和50mg变性超声小牛胸腺DNA,然后在补充有50μCi32-P-dCTP标记的探针的相同溶液中在-40℃下杂交18小时,然后洗涤三次 次,2xSSC,0.2%SDS,40℃30分钟; 或(c)编码具有SEQ ID NO:2的序列的氨基酸20-527的氨基酸序列的DNA序列。
摘要:
The present invention relates to isolated nucleic acid constructs containing a sequence encoding a Polyporus laccase, and the laccase proteins encoded thereby.
摘要:
The present invention relates to methods for producing heterologous heme proteins extracellularly comprising transforming a filamentous fungus with a vector comprising a DNA sequence encoding the heterologous heme protein and a DNA sequence encoding a preregion permitting secretion of the expressed heme protein, and culturing the transformed filamentous fungus in a suitable culture medium to produce the heme protein.
摘要:
The present invention relates to isolated nucleic acid constructs containing a sequence encoding a polyporus laccase, and the laccase proteins encoded thereby.
摘要:
Animal feed compositions and methods for treating one or more of soy, pea or rape-seed, or other material derived from Fabales or Cruciferaceae, with an enzyme having rhamnogalacturonase activity, wherein the enzyme having rhamnogalacturonase activity cleaves a rhamnogalacturonan backbone to produce rhamnose as a non-reducing end (RGase II) or cleaves a rhamnogalaturonan backbone to produce galacturonic acid as a non-reducing end.
摘要:
The present invention relates to an enzyme with .beta.-(1-6)-endoglucanase activity encoded by a DNA sequence, which DNA sequence a) comprises the DNA sequence shown in SEQ ID No. 3, or b) comprises an analogue of the DNA sequence shown in SEQ ID No. 3, which i) is homologous with the DNA sequences shown in or SEQ ID No. 3, and/or ii) hybridizes with the same oligonucleotide probe as the DNA sequence shown in SEQ ID No. 3, and/or iii) encodes a polypeptide which is homologous with the polypeptide encoded by a DNA sequence comprising the DNA sequence shown in SEQ ID No. 3, and/or iv) encodes a polypeptide which is immunologically reactive with an antibody raised against a purified .beta.-(1-6)-glucanase shown in SEQ ID No. 4 derived from Trichoderma harzianum, CBS 243.71. The present invention also relates to a DNA construct encoding the enzyme, a method of producing the enzyme, an enzyme preparation containing the enzyme, and the use of the enzyme and enzyme preparation for the degradation or modification of .beta.-glucan containing materials.
摘要翻译:本发明涉及由DNA序列编码的β-(1-6) - 内葡聚糖酶活性的酶,该DNA序列a)包含SEQ ID No.3所示的DNA序列,或b)包含DNA的类似物 序列号3所示的序列,其i)与SEQ ID No.3所示的DNA序列同源,和/或ii)与与SEQ ID No.3所示的DNA序列相同的寡核苷酸探针杂交, 和/或iii)编码与由包含SEQ ID No.3所示的DNA序列的DNA序列编码的多肽同源的多肽,和/或iv)编码与针对纯化的抗体产生的抗体具有免疫反应性的多肽 β-(1-6) - 葡聚糖酶,如SEQ ID No.4所示,源自哈茨木霉,CBS 243.71。 本发明还涉及编码该酶的DNA构建体,该酶的制备方法,含该酶的酶制剂,以及该酶和酶制剂用于含β-葡聚糖的材料的降解或修饰的用途。
摘要:
An isolated and purified enzyme exhibiting protease activity at a pH of 4-7 which exhibits protease activity in 5% hydrogen peroxide and which is encoded by a DNA sequence which hybridizes to a DNA sequence depicted in SEQ ID NO. 1 or 2.
摘要翻译:分离和纯化的酶,其在4-7的pH下显示蛋白酶活性,其在5%过氧化氢中显示蛋白酶活性,并且由与SEQ ID NO:1所示的DNA序列杂交的DNA序列编码。 1或2。