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    • 3. 发明申请
    • LIGATIONAL ENCODING OF SMALL MOLECULES
    • 小分子的编码
    • WO2004083427A3
    • 2005-02-17
    • PCT/DK2004000195
    • 2004-03-22
    • NUEVOLUTION ASFRANCH THOMASJACOBSEN SOEREN NYBOERASMUSSEN TORBENNEVE SOERENPEDERSEN HENRIKGOULIAEV ALEX HAAHR
    • FRANCH THOMASJACOBSEN SOEREN NYBOERASMUSSEN TORBENNEVE SOERENPEDERSEN HENRIKGOULIAEV ALEX HAAHR
    • C12N15/10C12P21/02
    • C07H21/04C12N15/1068C12P21/02C40B40/06C40B50/04
    • The invention relates to a method for synthesising a bifunctional complex comprising an encoded molecule and an identifier polynucleotide identifying the chemical entities having participated in the synthesis of the encoded molecule, said method comprising the steps of i) providing a) at least one template comprising one or more codons capable of hybridising to an anti-codon, wherein said template is optionally associated with one or more chemical entities, and b) a plurality of building blocks each comprising an anti-codon associated with one or more chemical entities, and ii) hybridising the anti-codon of one or more of the provided building blocks to the template, iii) covalently linking said anti-codons and/or linking the at least one template with the anti-codon of at least one building block, thereby generating an identifier polynucleotide capable of identifying chemical entities having participated in the synthesis of the encoded molecule, iv) separating the template from one or more of the anti-codons hybridised thereto, thereby generating an at least partly single stranded identifier polynucleotide associated with a plurality of chemical entities, v) generating a bifunctional complex comprising an encoded molecule and an identifier polynucleotide identifying the chemical entities having participated in the synthesis of the encoded molecule, wherein said encoded molecule is generated by reacting at least two of said plurality of chemical entities associated with the identifier polynucleotide, and wherein said at least two chemical entities are provided by separate building blocks.
    • 本发明涉及一种合成双功能复合物的方法,所述双功能复合物包含编码分子和识别已经参与编码分子合成的化学实体的标识多核苷酸,所述方法包括以下步骤:i)提供a)至少一个包含一个 或更多能够与抗密码子杂交的密码子,其中所述模板任选地与一个或多个化学实体相关联,以及b)多个结构单元,每个结构单元包含与一个或多个化学实体相关联的抗密码子,和ii) 将一个或多个所提供的构建块的抗密码子与模板杂交,iii)共价连接所述抗密码子和/或将至少一个模板与至少一个构建块的抗密码子连接,由此产生 能够识别已经参与编码分子的合成的化学实体的标识符多核苷酸,iv)将模板从一个或多个分离出来 更多的与其杂交的抗密码子,从而产生与多个化学实体相关联的至少部分单链标识多核苷酸,v)产生包含编码分子的双功能复合物和识别参与合成的化学实体的标识符多核苷酸 的编码分子,其中所述编码的分子通过使与所述标识多核苷酸相关联的所述多个化学实体中的至少两个反应而产生,并且其中所述至少两个化学实体由单独的构建块提供。
    • 9. 发明申请
    • FUNGAL LIPOLYTIC ENZYMES
    • 真菌脂肪酶
    • WO2005087918A9
    • 2006-08-24
    • PCT/IB2005000875
    • 2005-03-10
    • DANISCOBRUNSTEDT JANNEMIKKELSEN JOERN DALGAARDPEDERSEN HENRIKSOEE JOERN BORCH
    • BRUNSTEDT JANNEMIKKELSEN JOERN DALGAARDPEDERSEN HENRIKSOEE JOERN BORCH
    • C12N9/00A21D8/04A23C19/032A23K1/165A23K1/18A23L1/03A23L1/105A23L1/16A23L1/24C11B3/00C12N9/18
    • A21D8/042A23C19/0328A23D7/02A23K20/189A23K50/75A23L7/107A23L7/109A23L7/111A23L27/60A23L29/06C11B3/003C12N9/18C12P7/62C12P19/44C12Y301/01
    • A fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides, wherein the enzyme preferably has a phospholipidAriglyceride hydrolysing activity ratio of at least 4. Preferably, the lipolytic enzyme according to the present invention has a glycolipid:triglyceride hydrolysing activity ratio of at least 1.5. In one embodiment, the fungal lipolytic enzyme according to the present invention comprises an amino acid sequence as shown in SEQ ID No. 1 or SEQ ID No. 2 or SEQ ID No. 4 or SEQ ID No. 6 or an amino acid sequence which has at least 90% identity thereto. The present invention further encompasses a nucleic acid encoding a fungal lipolytic enzyme, which nucleic acid is selected from the group consisting of: (a) a nucleic acid comprising a nucleotide sequence shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7; (b) a nucleic acid which is related to the nucleotide sequence of SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7 by the degeneration of the genetic code; and (c) nucleic acid comprising a nucleotide sequence which has at least 90% identity with the nucleotide sequence shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7.
    • 与甘油三酸酯相比,极性脂质的活性比例更高的真菌野生型脂肪分解酶,其中该酶优选具有至少4个磷脂酸甘油酯水解活性比。优选地,根据本发明的脂肪分解酶具有糖脂:甘油三酯 水解活性比至少为1.5。 在一个实施方案中,根据本发明的真菌脂肪分解酶包含如SEQ ID No.1或SEQ ID No.2或SEQ ID No.4或SEQ ID No.6所示的氨基酸序列或氨基酸序列, 与其具有至少90%的同一性。 本发明还包括编码真菌脂肪分解酶的核酸,该核酸选自:(a)包含SEQ ID No.3,SEQ ID No.5或SEQ SEQ ID No.5所示核苷酸序列的核酸 第7号; (b)通过遗传密码的退化与SEQ ID No.3,SEQ ID No.5或SEQ ID No.7的核苷酸序列有关的核酸; 和(c)核酸,其包含与SEQ ID No.3,SEQ ID No.5或SEQ ID No.7所示的核苷酸序列具有至少90%同一性的核苷酸序列。
    • 10. 发明申请
    • ENCODED MOLECULES BY TRANSLATION (EMT)
    • 编码分子通过翻译(EMT)
    • WO2004110964A3
    • 2005-03-31
    • PCT/DK2004000416
    • 2004-06-15
    • NUEVOLUTION ASPEDERSEN HENRIKFRANCH THOMAS
    • PEDERSEN HENRIKFRANCH THOMAS
    • C07B61/00C12N15/10C12N15/67
    • C12N15/1062C12N15/1068C12N15/67
    • The present invention is directed to methods for the synthesis, selection, amplification and isolation of templated molecules having desirable properties. The invention makes it possible to synthesise a variety of different templated molecules other than alpha-peptides and modified alpha-peptides. In particular, the present invention enables synthesis of templated molecules such as beta -, ϒ -, ϖ peptides, carbopeptoids, vinylogous peptides, oligoanthrilamides, oligoureas, azapeptides (azatides), oligocarbamates, PNA, oligopyrrolinones, vinylogous sulfonamidopeptide, peptoids, azapeptoids and hydrazino peptides. It is possible in accordance with the methods of the invention to synthesise templated molecules comprising heterocyclic components, such as coumarins and quinolones, pyrazolone, isoxazolone, pyrimidiones, phtalhydrazides, diketopiperazines, hydantoins, and benzodiazepines.
    • 本发明涉及用于合成,选择,扩增和分离具有所需性质的模板分子的方法。 本发明使得可以合成除α-肽和修饰的α-肽以外的各种不同的模板分子。 特别地,本发明能够合成模板分子,例如β - ,Υ-,π肽,卡皮派,血液肽,寡聚甲酰胺,寡聚脲,azapeptides(azatides),oligocarbamates,PNA,oligopyrrolinones,vinylogous sulfamidopeptide,peptoids,azapeptoids和hydrazino 肽。 可以根据本发明的方法合成包含杂环成分的模板分子,例如香豆素和喹诺酮类,吡唑啉酮,异恶唑酮,嘧啶,邻苯二甲酰肼,二酮哌嗪,乙内酰脲和苯并二氮杂。