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    • 21. 发明授权
    • Alkaline protease
    • 碱性蛋白酶
    • US07368273B2
    • 2008-05-06
    • US10385662
    • 2003-03-12
    • Mitsuyoshi OkudaTsuyoshi SatoKazuhiro SaitoNobuyuki SumitomoYoshifumi IzawaKatsuhisa SaekiTohru KobayashiMasafumi Nomura
    • Mitsuyoshi OkudaTsuyoshi SatoKazuhiro SaitoNobuyuki SumitomoYoshifumi IzawaKatsuhisa SaekiTohru KobayashiMasafumi Nomura
    • C12N9/48C11D3/386
    • C11D3/386C12N9/54C12Y304/21062
    • An alkaline protease wherein an amino acid residue at (a) position 65, (b) position 101, (c) position 163, (d) position 17-0, (e) position 171, (f) position 273, (g) position 320, (h) position 359 or (i) position 387 of SEQ. ID NO: 2 or at a position corresponding thereto has been selected from the following amino acid residues: position (a): proline, position (b): asparagine, position (e): histidine, aspartic acid, phenylalanine, lysine, asparagine, seine, isoleucine, leucine, glutamine, threonine and valine, position (d): valine and leucine, position (e): alanine, glutamic acid, glycine and threonine, position (K): isoleucine, glycine and threonine, position (g): phenylalanine, valine, threonine, leucine, isoleucine and glycine, position (h): seine, leucine, valine, isoleucine and glutamine, position (i): alanine, lysine, glutamine, glutamic acid, arginine and histidine. A method to an alkaline protease having activity even in the presence of a highly concentrated fatty acid, and exhibiting excellent detergency for the removal of a complex stain containing protein, sebum and the like, and therefore useful as an ingredient in a detergent.
    • (a)位置65,(b)位置101,(c)位置163,(d)位置17-0,(e)位置171,(f)位置273,(g) 位置320,(h)位置359或(i)SEQ ID NO: 位置(a):脯氨酸,位置(b):天冬酰胺,位置(e):组氨酸,天冬氨酸,苯丙氨酸,赖氨酸,天冬酰胺, (e):丙氨酸,谷氨酸,甘氨酸和苏氨酸,位置(K):异亮氨酸,甘氨酸和苏氨酸,位置(g):缬氨酸和亮氨酸, (i):丙氨酸,赖氨酸,谷氨酰胺,谷氨酸,精氨酸和组氨酸,位置(h):ine碱,亮氨酸,缬氨酸,异亮氨酸和谷氨酰胺。 一种碱性蛋白酶的方法,即使在高度浓缩的脂肪酸的存在下也具有活性,并且对于去除含有蛋白质,皮脂等的复合污渍具有优异的去污力,因此可用作洗涤剂中的成分。
    • 22. 发明授权
    • Developing method and apparatus
    • 开发方法和装置
    • US07182531B2
    • 2007-02-27
    • US11476574
    • 2006-06-29
    • Kiyohisa TateyamaMasafumi NomuraTaketora Shinogi
    • Kiyohisa TateyamaMasafumi NomuraTaketora Shinogi
    • G03D5/00
    • G03D3/065G03D3/06G03F7/30G03F7/3071H01L21/6715H01L21/67253
    • In this developing method and apparatus, a concentration measuring unit 222 picks part of developing fluid in a blending tank 186 to measure the resist concentration by an absorption photometry and feeds the detected resist concentration to a control unit 240. The control unit 240 controls respective valves 210, 212, 216 of a TMAH concentrate solution 200, a solvent pipe 204 and a drain pipe 208 in a manner that the developing fluid in the blending tank 186 has a TMAH concentration corresponding to a measured resist-concentration value to accomplish a constant developing rate, performing component control of the developing fluid. The developing fluid transferred from the blending tank 186 to a supply tank 188 is fed to a developer nozzle DN in a developing section 126 through a developer pipe 224 owing to the drive of a pump 228. Accordingly, even if the developing fluid is reused in the developing process in multiple times, it is possible to make sure of the uniformity in development.
    • 在该显影方法和装置中,浓度测量单元222拾取混合罐186中的显影液的一部分,通过吸收测光法测量抗蚀剂浓度,并将检测到的抗蚀剂浓度输送到控制单元240.控制单元240控制各个阀 210,212,216的TMAH浓缩液200,溶剂管204和排水管208,使得混合罐186中的显影液具有对应于测量的抗蚀剂浓度值的TMAH浓度,以实现恒定显影 速率,执行显影液的成分控制。 从混合罐186输送到供给罐188的显影液由于泵228的驱动而通过显影管224被供给到显影部126中的显影剂喷嘴DN。因此,即使显影液再利用 发展过程多次,有可能确保发展的一致性。
    • 23. 发明申请
    • Developing method and apparatus
    • 开发方法和装置
    • US20060246384A1
    • 2006-11-02
    • US11476574
    • 2006-06-29
    • Kiyohisa TateyamaMasafumi NomuraTaketora Shinogi
    • Kiyohisa TateyamaMasafumi NomuraTaketora Shinogi
    • G03C1/005
    • G03D3/065G03D3/06G03F7/30G03F7/3071H01L21/6715H01L21/67253
    • In this developing method and apparatus, a concentration measuring unit 222 picks part of developing fluid in a blending tank 186 to measure the resist concentration by an absorption photometry and feeds the detected resist concentration to a control unit 240. The control unit 240 controls respective valves 210, 212, 216 of a TMAH concentrate solution 200, a solvent pipe 204 and a drain pipe 208 in a manner that the developing fluid in the blending tank 186 has a TMAH concentration corresponding to a measured resist-concentration value to accomplish a constant developing rate, performing component control of the developing fluid. The developing fluid transferred from the blending tank 186 to a supply tank 188 is fed to a developer nozzle DN in a developing section 126 through a developer pipe 224 owing to the drive of a pump 228. Accordingly, even if the developing fluid is reused in the developing process in multiple times, it is possible to make sure of the uniformity in development.
    • 在该显影方法和装置中,浓度测量单元222拾取混合罐186中的显影液的一部分,通过吸收测光法测量抗蚀剂浓度,并将检测到的抗蚀剂浓度输送到控制单元240.控制单元240控制各个阀 210,212,216的TMAH浓缩液200,溶剂管204和排水管208,使得混合罐186中的显影液具有对应于测量的抗蚀剂浓度值的TMAH浓度,以实现恒定显影 速率,执行显影液的成分控制。 从混合罐186输送到供给罐188的显影液由于泵228的驱动而通过显影管224被供给到显影部126中的显影剂喷嘴DN。因此,即使显影液再利用 发展过程多次,有可能确保发展的一致性。
    • 29. 发明申请
    • ALKALINE PROTEASE
    • 碱性蛋白酶
    • US20080177040A1
    • 2008-07-24
    • US12049022
    • 2008-03-14
    • Mitsuyoshi OkudaTsuyoshi SatoKazuhiro SaitoNobuyuki SumitomoYoshifumi IzawaKatsuhisa SaekiTohru KobayashiMasafumi Nomura
    • Mitsuyoshi OkudaTsuyoshi SatoKazuhiro SaitoNobuyuki SumitomoYoshifumi IzawaKatsuhisa SaekiTohru KobayashiMasafumi Nomura
    • C07K2/00
    • C11D3/386C12N9/54C12Y304/21062
    • Provided in the present invention is an alkaline protease wherein an amino acid residue at (a) position 65, (b) position 101, (c) position 163, (d) position 170, (e) position 171, (f) position 273, (g) position 320, (h) position 359 or (i) position 387 of SEQ. ID NO:1 or at a position corresponding thereto has been selected from the following amino acid residues: position (a): proline, position (b): asparagine, position (c): histidine, aspartic acid, phenylalanine, lysine, asparagine, serine, isoleucine, leucine, glutamine, threonine and valine, position (d): valine and leucine, position (e): alanine, glutamic acid, glycine and threonine, position (f): isoleucine, glycine and threonine, position (g): phenylalanine, valine, threonine, leucine, isoleucine and glycine, position (h): serine, leucine, valine, isoleucine and glutamine, position (i): alanine, lysine, glutamine, glutamic acid, arginine and histidine.The present invention makes it possible to efficiently produce and provide alkaline proteases having activity even in the presence of a highly concentrated fatty acid, and exhibiting excellent detergency for the removal of a complex stain containing protein, sebum and the like, and therefore being useful as an enzyme to be incorporated in a detergent.
    • 在本发明中提供的是碱性蛋白酶,其中(a)位置65,(b)位置101,(c)位置163,(d)位置170,(e)位置171,(f) ,(g)位置320,(h)位置359或(i)SEQ ID NO: 位置(a):脯氨酸,位置(b):天冬酰胺,位置(c):组氨酸,天冬氨酸,苯丙氨酸,赖氨酸,天冬酰胺, 位置(d):缬氨酸和亮氨酸,位置(e):丙氨酸,谷氨酸,甘氨酸和苏氨酸,位置(f):异亮氨酸,甘氨酸和苏氨酸,位置(g) 位置(h):丝氨酸,亮氨酸,缬氨酸,异亮氨酸和谷氨酰胺,位置(i):丙氨酸,赖氨酸,谷氨酰胺,谷氨酸,精氨酸和组氨酸,位置(h):缬氨酸,缬氨酸,苏氨酸,亮氨酸,异亮氨酸和甘氨酸。 本发明使得可以有效地生产和提供具有活性的碱性蛋白酶,即使在高度浓缩的脂肪酸的存在下也具有优异的去污力来去除含有蛋白质,皮脂等的复合污渍,因此可用作 要掺入洗涤剂中的酶。
    • 30. 发明授权
    • Alkaline protease
    • 碱性蛋白酶
    • US07101698B2
    • 2006-09-05
    • US10456479
    • 2003-06-09
    • Tsuyoshi SatoMitsuyoshi OkudaYasushi TakimuraNobuyuki SumitomoMasafumi NomuraTohru Kobayashi
    • Tsuyoshi SatoMitsuyoshi OkudaYasushi TakimuraNobuyuki SumitomoMasafumi NomuraTohru Kobayashi
    • C12N9/54C12N15/74C12P21/00C07K14/32
    • C07H21/04C12N9/54
    • The present invention relates to an alkaline protease having a prepro sequence, wherein the prepro sequence is a mutant sequence of the amino acid sequence of SEQ ID NO: 1 or an amino acid sequence having 80% or higher homology to the amino acid sequence of SEQ ID NO: 1, in which amino acid residues at (a) position 52, (b) position 75, and (c) position 142 of SEQ ID NO: 1, or amino acid residues at positions corresponding to these positions are substituted by the following amino acid residues: at position (a): aspartic acid or arginine, at position (b): alanine or arginine, and at position (c): lysine; and the alkaline protease, when in a mature form, has the amino acid sequence of SEQ ID NO: 2 or an amino acid sequence having a homology of 80% or higher to this amino acid sequence. The present invention also relates to, for example, a gene encoding the alkaline protease. According to the present invention, an alkaline protease increased in production can be produced. In particular, there can be efficiently produced an alkaline protease having an activity even in the presence of a fatty acid of high concentration and exhibiting excellent detergency against complex soils containing proteins and sebum.
    • 本发明涉及具有前序列的碱性蛋白酶,其中前序列是SEQ ID NO:1的氨基酸序列的突变序列或与SEQ ID NO:1的氨基酸序列具有80%以上同源性的氨基酸序列 SEQ ID NO:1的(a)位置52,(b)位置75和(c)位置142处的氨基酸残基或对应于这些位置的位置处的氨基酸残基被替换为SEQ ID NO: 以下氨基酸残基:位置(a):天冬氨酸或精氨酸,位置(b):丙氨酸或精氨酸,和位置(c):赖氨酸; 碱性蛋白酶以成熟形式具有SEQ ID NO:2的氨基酸序列或与该氨基酸序列同源性为80%以上的氨基酸序列。 本发明还涉及例如编码碱性蛋白酶的基因。 根据本发明,可以生产生产中增加的碱性蛋白酶。 特别是,即使在高浓度的脂肪酸的存在下也能够有效地生成具有活性的碱性蛋白酶,并且对于含有蛋白质和皮脂的复杂土壤表现出优异的去污力。