摘要:
The present invention relates to isolated DNA sequences which code for the expression of plant 1-deoxy-D-xylulose-5-phosphate reductoisomerase protein, such as the sequence presented in SEQ ID NO:1 which encodes a 1-deoxy-D-xylulose-5-phosphate reductoisomerase protein from peppermint (Mentha x piperita). Additionally, the present invention relates to isolated plant 1-deoxy-D-xylulose-5-phosphate reductoisomerase protein. In other aspects, the present invention is directed to replicable recombinant cloning vehicles comprising a nucleic acid sequence which codes for a plant 1-deoxy-D-xylulose-5-phosphate reductoisomerase, to modified host cells transformed, transfected, infected and/or injected with a recombinant cloning vehicle and/or DNA sequence of the invention.
摘要翻译:本发明涉及编码植物1-脱氧-SMALLCAPS> D D SMALLCAPS> - 5-羟基-5-磷酸还原异构酶蛋白。 此外,本发明涉及分离的植物1-脱氧-β-氧化物-5-磷酸还原异构酶蛋白。 在其它方面,本发明涉及可复制的重组克隆载体,其包含编码植物1-脱氧-SMALLCAPS> D / /SMALLCAPSα-羟基-5-磷酸还原异构酶的核酸序列,转化的修饰的宿主细胞, 转染,感染和/或注射本发明的重组克隆载体和/或DNA序列。
摘要:
Disclosed are isolated polypeptides having glucose isomerase activity selected from: (a) a polypeptide having an amino acid sequence which has at least 95% identity with amino acids of SEQ ID NO:2; (b) a variant of the polypeptide having an amino acid sequence of SEQ ID NO:2 comprising a substitution, deletion, and/or insertion of one or more amino acids; (c) a fragment of (a) that has glucose isomerase activity; and (d) a polypeptide having a pH optimum in the range of 5.7 to 6.3 at 60° C., a pH optimum in the range of 6.1 to 6.7 at 90° C and a temperature optimum of above 90° C. Also disclosed are isolated nucleic acid sequences encoding the polypeptides, nucleic acid constructs, vectors, and host cells comprising the nucleic acid sequences as well as methods for producing and using the polypeptides.
摘要翻译:公开了具有选自以下的葡萄糖异构酶活性的分离的多肽:(a)具有与SEQ ID NO:2的氨基酸具有至少95%同一性的氨基酸序列的多肽;(b)具有氨基酸的多肽的变体 包含一个或多个氨基酸的取代,缺失和/或插入的SEQ ID NO:2的序列;(c)具有葡萄糖异构酶活性的(a)的片段; 和(d)在60℃下pH最佳为5.7至6.3的多肽,在90℃下最佳为6.1至6.7,最适温度为90℃以上的pH最佳。 分离的编码多肽的核酸序列,核酸构建体,载体和包含核酸序列的宿主细胞以及产生和使用多肽的方法。
摘要:
The invention concerns novel polypeptides capable of interacting with the human topoisomerase III&agr; and the nucleic acid sequences coding for said polypeptides. The invention also concerns a method for identifying compounds capable of interacting with said polypeptides and a method for identifying molecules capable of modulating the interaction of the topoisomerase III&agr; with said polypeptides.
摘要:
A novel topoisomerase IV, nucleotide sequences coding for said enzyme, corresponding vectors, and the use of said enzyme for screening biologically active materials.
摘要:
There are provided a DNA coding for phosphohexuloisomerase, which is a protein defined in the following (A) or (B), and a method for producing the enzyme: (A) a protein having the amino acid sequence of SEQ ID NO: 3 shown in Sequence Listing, (B) a protein having the amino acid sequence of SEQ ID NO: 3 shown in Sequence Listing including substitution, deletion, insertion or addition of one or several amino acid residues and having phosphohexulose isomerase activity.
摘要翻译:提供了编码以下(A)或(B)中定义的蛋白质的磷酸己糖异构酶的DNA及其制造方法:(A)具有SEQ ID NO:3的氨基酸序列的蛋白质 (B)具有序列表所示的氨基酸序列SEQ ID NO:3的蛋白质,其包含一个或几个氨基酸残基的取代,缺失,插入或添加并具有磷酸己糖糖异构酶活性。
摘要:
Hexulose phosphate synthase was purified from Mycobacterium gastri to determine an amino acid sequence of the enzyme. Oligonucleotide primers to be used for PCR were synthesized on the basis of obtained amino acid sequence information. A DNA fragment, which was amplified by performing PCR by using a template of genomic DNA prepared from Mycobacterium gastri, was used as a probe so that colony hybridization was carried out with respect to a library comprising fragments obtained by digesting Mycobacterium gastri genomic DNA with PstI to obtain a positive clone. Thus, the DNA fragment which contains ORF encoding hexulose phosphate synthase was obtained. Furthermore, the DNA fragment cloned contained other ORF(ORF-1). The expression system of ORF-1 was constructed (pT-HPIS-1), and it was introduced into Escherichia coli cell. After the induction of the expression of ORF-1, the hexulose phosphate isomerase activity was found in the extract of cells harvoring pT-HPIS-1. Thus, gene, which coded for hexulose phosphate isomerase, was obtained together with ORF which coded for hexulose phosphate synthase.
摘要:
The present invention relates to a method of isolating an enzyme having a desired chemical or biological activity, the method comprising linking the enzyme to a substrate for the enzyme, reacting the enzyme and substrate such that a product is produced which remains linked to the enzyme and isolating the enzyme by selectively isolating the product linked to the enzyme.
摘要:
The present invention relates to a 5-substituted hydantoin racemase, which efficiently catalyzes racemization reactions at a high optimum temperature for racemization reactions, DNA coding for the racemase, and processes for producing optically active amino acids.
摘要:
The present invention relates to the use of these cyclophilins, hereinafter referred to as ‘tyrosine-containing’ cyclophilins, in a method for identifying compounds capable of binding to and/or inhibiting the enzymatic activity of these proteins. Such compounds may be further screened for their ability to inhibit parasites which are not susceptible to the anti-parasitic effects of CsA.