摘要:
Alkaline protease which has leucine or isoleucine in the place of valine at the amino acid number 40 of wild type alkaline protease, a gene encoding the amino acid sequence of alkaline protease which has the substitution as described above, a recombinant DNA comprising said gene, a method of producing the above described alkaline protease, and a DNA fragment used for the expression of a gene.
摘要:
The present invention relates to luminescent playthings such as candles, table lights, pen lights, illumination, illuminating playthings for camp, illuminating playthings for night fishing, fish-gathering lamps, safety candles, neon lights, luminescent inks, luminescent pens, luminescent coatings or luminescent writing implements, in which a soft light of an indescribable tone of color not obtainable from flames of conventional candles is emitted via seawater, lake and marsh water, river water, ground water, tap water or mineral drinking water by utilizing 3 components of luciferin, luciferase and ATP or 4 components of these components plus a metal salt, out of components necessary for bioluminescence in fireflies.
摘要:
A purified luciferase from Luciola lateralis is disclosed. The enzyme is characterized by having properties including: an optimum pH range of 7.5 to 9.5, an optimum temperature range of 0.degree. C. to 50.degree. C., and that the enzyme does not act on ADP, CTP, UTP, and GTP. The enzyme is purified by using a process which includes: gel filtration chromatography, hydroxyapatite column chromatography, and a tris(hydroxy)aminomethane-hydro-chloric acid buffer.
摘要:
Disclosed is a purified luciferase and a method for making it. The luciferase is obtained from Luciola cruciata. The luciferase has a pH range for stabililty of 6.5-9.0 and a optimum pH range of 8.0-9.5. The enzyme does not act on ADP, CTP, UTP and GTP.
摘要:
The present invention provides an improved mink growth hormone gene, a recombinant DNA containing the improved mink growth hormone gene, microorganisms which belong to the genus Escherichia and contain the recombinant DNA and which are capable of producing a mink growth hormone, and a method for producing a mink growth hormone using the E.coli transformant containing the recombinant DNA. According to the present invention, a mink growth hormone is efficiently produced.
摘要:
A luciferase gene isolated from Luciola cruciata (Japanese firefly) coding for an amino acid sequence shown in FIG. 4 and a novel recombinant DNA characterized by incorporating a gene coding for luciferase into a vector DNA are disclosed. There is also disclosed a method of producing luciferase which comprises culturing in a medium a microorganism containing a recombinant DNA having inserted a gene coding for luciferase in a vector DNA and belonging to the genus Escherichia capable of producing luciferase and collecting luciferase from the culture.
摘要:
The present invention relates to variant E.sub.1 protein of pyruvate dehydrogenase complex of high activity in which arginine at the 146-position is replaced by proline in the amino acid sequence of wild-type E.sub.1 protein of pyruvate dehydrogenase complex, a gene coding for said variant E.sub.1 protein, a novel recombinant DNA comprising said variant E.sub.1 protein-encoding gene inserted in a vector DNA, and a process for producing variant E.sub.1 protein by said recombinant DNA. The present invention provides the variant E.sub.1 protein of pyruvate dehydrogenase complex of high activity.
摘要:
The present invention provides a method of controlling an electrocoating bath using an ion exchange resin. The ion exchange resin is maintained in a porous container in a suspended state in the electrocoating bath, and is used in a quantity of not more than the chemical equivalent of excess counter-ion to be removed from the bath. Bath control is easily achieved without any coagulation trouble as often observed in conventional column methods.
摘要:
The present invention relates to a DNA fragment of 3,563 base pairs containing a gene coding for tannase and derived from a microorganism belonging to the genus Aspergillus, with the following restriction enzyme map: ##STR1## B: Bam HI, H: Hind III, K: Kpn I, S: Sal I, X: Xba I; a DNA fragment containing a tannase gene coding for the amino acid sequence of (SEQ ID NO:4); a recombinant plasmid comprising the DNA fragment containing the tannase gene inserted into a plasmid vector; a process for producing tannase, comprising culturing a microorganism belonging to the genus Aspergillus capable of producing tannase in medium with the recombinant plasmid, and recovering tannase from the culture; and a promoter represented by the nucleotide sequence of (SEQ ID NO:1). Tannase can be efficiently produced according to the present invention.
摘要翻译:本发明涉及含有编码鞣酸酶的基因并衍生自属于曲霉属的微生物的3,563个碱基对的DNA片段,其具有以下限制酶图:B:Bam HI,H:Hind III,K :Kpn I,S:Sal I,X:Xba I; 含有编码(SEQ ID NO:4)的氨基酸序列的鞣酸酶基因的DNA片段; 包含插入质粒载体中的含有鞣酸酶基因的DNA片段的重组质粒; 一种鞣酸酶的制造方法,其特征在于,在培养基中培养能够在培养基中生产鞣酸酶的微生物属于属于曲霉属的微生物,从培养物中回收鞣酸酶; 和由(SEQ ID NO:1)的核苷酸序列表示的启动子。 根据本发明可以有效地制备鞣酸酶。
摘要:
A method for the pretreatment of a long cloth continuously in which a cloth to be subjected to desizing, scouring and bleaching for the pretreatment thereof is preliminarily subjected to souring treatment in the sodium chlorite solution prepared by absorbing the chlorine dioxide gas, which is exhausted from the subsequent bleaching process with the use of chlorite, in a solution of H.sub.2 O.sub.2 and NaOH, and accordingly it is possible to transport the long cloth continuously in the pretreating process speedily with no need of staying the cloth in folded state for increasing the productivity and improving the quality of the product, and further to render the pretreating apparatus compact so as suitable for the production of small lot products.