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公开(公告)号:US20100217032A1
公开(公告)日:2010-08-26
申请号:US12518713
申请日:2007-12-11
申请人: Paul Klaassen , Adrianus Wilhelmus Hermanus Vollebregt , Marco Alexander Van Den Berg , Marcus Hans , Jan Metske Van Der Laan
发明人: Paul Klaassen , Adrianus Wilhelmus Hermanus Vollebregt , Marco Alexander Van Den Berg , Marcus Hans , Jan Metske Van Der Laan
IPC分类号: C12P7/62 , C07K14/195 , C07H21/04 , C07C69/34
CPC分类号: C12P7/42 , C12N9/0077 , C12P7/62
摘要: The present invention provides a polypeptide having an amino acid sequence according to SEQ ID NO 3, SEQ ID NO 6 or SEQ ID NO 43-59. The present invention also provides a polynucleotide comprising a DNA sequence encoding these polypeptides and a method for isolating polynucleotides encoding polypeptides capable of improving the compactin into pravastatin conversion. Furthermore, the present invention provides a method for producing pravastatin and a pharmaceutical composition comprising pravastatin.
摘要翻译: 本发明提供具有根据SEQ ID NO 3,SEQ ID NO 6或SEQ ID NO 43-59的氨基酸序列的多肽。 本发明还提供了一种包含编码这些多肽的DNA序列的多核苷酸,以及一种分离编码多肽的方法,所述多核苷酸能够将该致密蛋白改进普伐他汀转化。 此外,本发明提供了普伐他汀的制造方法和含有普伐他汀的药物组合物。
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公开(公告)号:US20100009404A1
公开(公告)日:2010-01-14
申请号:US12444108
申请日:2007-10-02
CPC分类号: C12N9/0004
摘要: The present invention describes a process for the production of an N-α-amino-hydroxyphenylacetyl or an N-α-aminophenylacetyl β-lactam antibiotic comprising an IPNS-catalysed conversion of a precursor tripeptide hydroxyphenylglycyl-cysteinyl-valine (HpgCV) or phenylglycyl-cysteinyl-valine (PgCV), respectively, to the N-hydroxyphenylglycyl or the N-phenylglycyl β-lactam antibiotic, respectively. The tripeptide HpgCV or the tripeptide PgCV may further be prepared by contacting the amino acids hydroxyphenylglycine (Hpg) or phenylglycine (Pg), cystein (C) and valine (V) with a non-ribosomal peptide synthetase (NRPS) to effect formation of the tripeptide HpgCV or the tripeptide PgCV, the NRPS comprising a first module M1 specific for Hpg or Pg, a second module M2 specific for C and a third module M3 specific for V An IPNS is further provided having an improved activity in this conversion, as well as an NRPS catalysing the formation of the tripeptides. Also a host cell is provided capable of fermentatively producing β-lactam antibiotics with N-α-amino-hydroxyphenylacetyl or an N-α-aminophenylacetyl side chains.
摘要翻译: 本发明描述了制备N-α-氨基 - 羟基苯基乙酰基或N-α-氨基苯基乙酰基β-内酰胺抗生素的方法,其包括前体三肽羟基苯基甘氨酰 - 半胱氨酰 - 缬氨酸(HpgCV)或苯基甘氨酰 - 半胱氨酰缬氨酸(PgCV)分别分别与N-羟基苯基甘氨酰或N-苯基甘氨酰β-内酰胺抗生素。 三肽HpgCV或三肽PgCV可以通过使氨基酸羟基苯基甘氨酸(Hpg)或苯基甘氨酸(Pg),半胱氨酸(C)和缬氨酸(V)与非核糖体肽合成酶(NRPS)接触来进一步制备,以形成 三肽HpgCV或三肽PgCV,NRPS包括特定于Hpg或Pg的第一模块M1,特定于C的第二模块M2和特定于V An IPNS的第三模块M3,还具有在该转换中具有改进的活性 作为催化三肽形成的NRPS。 还提供了能够用N-α-氨基 - 羟基苯基乙酰基或N-α-氨基苯乙酰侧链发酵生产β-内酰胺抗生素的宿主细胞。
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公开(公告)号:US08293511B2
公开(公告)日:2012-10-23
申请号:US12444108
申请日:2007-10-02
CPC分类号: C12N9/0004
摘要: The present invention describes a process for the production of an N-α-amino-hydroxyphenylacetyl or an N-α-aminophenylacetyl β-lactam antibiotic comprising an IPNS-catalysed conversion of a precursor tripeptide hydroxyphenylglycyl-cysteinyl-valine (HpgCV) or phenylglycyl-cysteinyl-valine (PgCV), respectively, to the N-hydroxyphenylglycyl or the N-phenylglycyl β-lactam antibiotic, respectively. The tripeptide HpgCV or the tripeptide PgCV may further be prepared by contacting the amino acids hydroxyphenylglycine (Hpg) or phenylglycine (Pg), cystein (C) and valine (V) with a non-ribosomal peptide synthetase (NRPS) to effect formation of the tripeptide HpgCV or the tripeptide PgCV, the NRPS comprising a first module M1 specific for Hpg or Pg, a second module M2 specific for C and a third module M3 specific for V An IPNS is further provided having an improved activity in this conversion, as well as an NRPS catalysing the formation of the tripeptides. Also a host cell is provided capable of fermentatively producing β-lactam antibiotics with N-α-amino-hydroxyphenylacetyl or an N-α-aminophenylacetyl side chains.
摘要翻译: 本发明描述了一种制备N-α-氨基 - 羟基苯基乙酰基或N-α-氨基苯基乙酰基 - 内酰胺抗生素的方法,其包括前体三肽羟基苯基甘氨酰 - 半胱氨酰 - 缬氨酸(HpgCV)或苯基甘氨酰 - 半胱氨酰缬氨酸(PgCV)分别转化为N-羟基苯基甘氨酰或N-苯基甘氨酰和β-内酰胺抗生素。 三肽HpgCV或三肽PgCV可以通过使氨基酸羟基苯基甘氨酸(Hpg)或苯基甘氨酸(Pg),半胱氨酸(C)和缬氨酸(V)与非核糖体肽合成酶(NRPS)接触来进一步制备,以形成 三肽HpgCV或三肽PgCV,NRPS包括特定于Hpg或Pg的第一模块M1,特定于C的第二模块M2和特定于V An IPNS的第三模块M3,还具有在该转换中具有改进的活性 作为催化三肽形成的NRPS。 还提供了能够用N-α-氨基 - 羟基苯基乙酰基或N-α-氨基苯乙酰侧链发酵生产β-内酰胺抗生素的宿主细胞。
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公开(公告)号:US20120034648A1
公开(公告)日:2012-02-09
申请号:US12867927
申请日:2009-03-05
申请人: Paul Klaassen , Jan Metske Van Der Laan , Bianca Elisabeth Maria Gielesen , Gijsberdina Pieternella Van Suylekom
发明人: Paul Klaassen , Jan Metske Van Der Laan , Bianca Elisabeth Maria Gielesen , Gijsberdina Pieternella Van Suylekom
IPC分类号: C12P37/00 , C12N1/14 , C12N1/15 , C12N1/19 , C12P1/00 , C12P7/06 , C12P7/16 , C12P7/56 , C12P7/52 , C12P7/54 , C12P7/48 , C12P7/46 , C12P7/44 , C12P13/04 , C12P7/18 , C12P7/20 , C12P35/00 , C12N1/16
摘要: The invention relates to a cell which comprises a nucleotide sequence encoding a xylose isomerase, wherein the amino acid sequence of the xylose isomerase has at least about 70% sequence identity to the amino acid sequence set out in SEQ ID NO: 3 and wherein the nucleotide sequence is heterologous to the host. A cell of the invention may be used in a process for producing a fermentation product, such as ethanol. Such a process may comprise fermenting a medium containing a source of xylose with a cell of the invention such that the cell ferments xylose to the fermentation product.
摘要翻译: 本发明涉及包含编码木糖异构酶的核苷酸序列的细胞,其中木糖异构酶的氨基酸序列与SEQ ID NO:3所示的氨基酸序列具有至少约70%的序列同一性,其中所述核苷酸 序列与宿主异源。 本发明的细胞可用于生产发酵产物如乙醇的方法中。 这样的方法可以包括用本发明的细胞发酵含有木糖来源的培养基,使得细胞向发酵产物发酵木糖。
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公开(公告)号:US08399215B2
公开(公告)日:2013-03-19
申请号:US12867927
申请日:2009-03-05
申请人: Paul Klaassen , Jan Metske Van Der Laan , Bianca Elisabeth Maria Gielesen , Gijsberdina Pieternella Van Suylekom
发明人: Paul Klaassen , Jan Metske Van Der Laan , Bianca Elisabeth Maria Gielesen , Gijsberdina Pieternella Van Suylekom
摘要: The invention relates to a cell which comprises a nucleotide sequence encoding a xylose isomerase, wherein the amino acid sequence of the xylose isomerase has at least about 70% sequence identity to the amino acid sequence set out in SEQ ID NO: 3 and wherein the nucleotide sequence is heterologous to the host. The cell of the invention may be used in a process for producing a fermentation product, such as ethanol. Such a process may comprise fermenting a medium containing a source of xylose with a cell of the invention such that the cell ferments xylose to the fermentation product.
摘要翻译: 本发明涉及包含编码木糖异构酶的核苷酸序列的细胞,其中木糖异构酶的氨基酸序列与SEQ ID NO:3所示的氨基酸序列具有至少约70%的序列同一性,其中所述核苷酸 序列与宿主异源。 本发明的细胞可以用于生产发酵产物如乙醇的方法。 这样的方法可以包括用本发明的细胞发酵含有木糖来源的培养基,使得细胞向发酵产物发酵木糖。
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公开(公告)号:US20090233287A1
公开(公告)日:2009-09-17
申请号:US12298191
申请日:2007-04-25
申请人: Roelof Ary Lans Bovenberg , Marco Alexander Van den Berg , Susanne Hage , Paul Klaassen , Bernard Meijrink , Lourina Madeleine Raamsdonk
发明人: Roelof Ary Lans Bovenberg , Marco Alexander Van den Berg , Susanne Hage , Paul Klaassen , Bernard Meijrink , Lourina Madeleine Raamsdonk
CPC分类号: C12N9/1029 , C12N9/0004 , C12N9/93 , C12P7/02 , C12P13/02 , C12P17/06 , C12P17/181 , C12P17/182 , C12P17/188
摘要: The present invention provides a recombinant Penicillium chrysogenum strain characterized in that a gene selected from the list consisting of penDE, pcbAB and pcbC is inactivated and the use of such a strain for the preparation of a compound of interest. Furthermore, it is an object of the present invention to provide a method for the production of a compound of interest in a eukaryotic recombinant microorganism comprising the steps of: (a) Reducing the level of secondary metabolite production in said microorganism with 50-100%; (b) Introducing a heterologous gene into said microorganism
摘要翻译: 本发明提供重组产黄青霉菌株,其特征在于,从PenDE,pcbAB和pcbC列表中选出的基因被灭活,并且使用这样的菌株来制备感兴趣的化合物。 此外,本发明的目的是提供一种在真核重组微生物中生产感兴趣的化合物的方法,包括以下步骤:(a)降低所述微生物中次级代谢产物的产生水平,其中50-100% ; (b)将异源基因引入所述微生物
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公开(公告)号:US20140162312A1
公开(公告)日:2014-06-12
申请号:US14236191
申请日:2012-08-02
IPC分类号: C12N15/81 , C12P7/16 , C12P7/56 , C12P7/42 , C12P7/40 , C12P35/00 , C12P7/46 , C12P7/48 , C12P7/18 , C12P5/02 , C12P7/20 , C12P7/06 , C12P7/54
CPC分类号: C12N15/81 , C12N9/92 , C12N15/815 , C12P5/026 , C12P7/06 , C12P7/10 , C12P7/16 , C12P7/18 , C12P7/20 , C12P7/40 , C12P7/42 , C12P7/46 , C12P7/48 , C12P7/54 , C12P7/56 , C12P35/00 , C12Y503/01005 , Y02E50/16 , Y02E50/17
摘要: The invention relates to a cell which comprises a nucleotide sequence encoding a xylose isomerase, wherein the amino acid sequence of the xylose isomerase has at least 75% sequence identity to the amino acid sequence set out in SEQ ID NO: 2 and wherein the nucleotide sequence is heterologous to the host. A cell of the invention may be used in a process for producing a fermentation product, such as ethanol. Such a process may comprise fermenting a medium containing a source of xylose with a cell of the invention such that the cell ferments xylose to the fermentation product.
摘要翻译: 本发明涉及包含编码木糖异构酶的核苷酸序列的细胞,其中所述木糖异构酶的氨基酸序列与SEQ ID NO:2所示的氨基酸序列具有至少75%的序列同一性,并且其中所述核苷酸序列 与宿主异源。 本发明的细胞可用于生产发酵产物如乙醇的方法中。 这样的方法可以包括用本发明的细胞发酵含有木糖来源的培养基,使得细胞向发酵产物发酵木糖。
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公开(公告)号:US6159725A
公开(公告)日:2000-12-12
申请号:US783045
申请日:1997-01-16
IPC分类号: C12G1/00 , A21D8/04 , C07K14/395 , C12C11/00 , C12C11/02 , C12G1/022 , C12N1/19 , C12N15/09 , C12N15/81 , C12P7/06 , C12R1/865 , C12N1/16 , C12P21/06
CPC分类号: C12C12/006 , A21D8/047 , C07K14/395 , C12C12/004 , C12G1/0203 , C12N15/81 , Y02E50/17
摘要: Transformed yeasts are provided which constitutively express a hexose transporter gene. The transformed yeast can be used in the beer, bread, wine and whisky production.
摘要翻译: 提供了组成型表达己糖转运蛋白基因的转化酵母。 转化酵母可用于啤酒,面包,葡萄酒和威士忌生产。
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公开(公告)号:US09701972B2
公开(公告)日:2017-07-11
申请号:US14236191
申请日:2012-08-02
IPC分类号: C12N15/81 , C12N9/92 , C12P7/10 , C12P7/16 , C12P7/18 , C12P7/20 , C12P7/40 , C12P7/42 , C12P7/46 , C12P7/48 , C12P7/54 , C12P7/56 , C12P5/02 , C12P7/06 , C12P35/00
CPC分类号: C12N15/81 , C12N9/92 , C12N15/815 , C12P5/026 , C12P7/06 , C12P7/10 , C12P7/16 , C12P7/18 , C12P7/20 , C12P7/40 , C12P7/42 , C12P7/46 , C12P7/48 , C12P7/54 , C12P7/56 , C12P35/00 , C12Y503/01005 , Y02E50/16 , Y02E50/17
摘要: The invention relates to a cell which comprises a nucleotide sequence encoding a xylose isomerase, wherein the amino acid sequence of the xylose isomerase has at least 75% sequence identity to the amino acid sequence set out in SEQ ID NO: 2 and wherein the nucleotide sequence is heterologous to the host. A cell of the invention may be used in a process for producing a fermentation product, such as ethanol. Such a process may comprise fermenting a medium containing a source of xylose with a cell of the invention such that the cell ferments xylose to the fermentation product.
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公开(公告)号:US09034608B2
公开(公告)日:2015-05-19
申请号:US13822288
申请日:2011-10-11
申请人: Hendrik Wouter Wisselink , Antonius Jeroen Adriaan Van Maris , Jacobus Thomas Pronk , Paul Klaassen , Rene Marcel De Jong
发明人: Hendrik Wouter Wisselink , Antonius Jeroen Adriaan Van Maris , Jacobus Thomas Pronk , Paul Klaassen , Rene Marcel De Jong
IPC分类号: C12P19/18 , C12P7/56 , C12P7/16 , C12P7/06 , C12P7/14 , C12N9/12 , C12N1/00 , C12P21/06 , C12P19/34 , C12N15/00 , C07H21/04 , C07K1/00 , C12N15/81 , C07K14/395 , C12P7/10
CPC分类号: C12N15/81 , C07K14/395 , C12N9/1205 , C12P7/06 , C12P7/10 , Y02E50/16 , Y02E50/17
摘要: The invention relates to a polypeptide having a mutation at one or more position corresponding to T219 of SEQ ID NO: 55, wherein the polypeptide has at least 50% sequence identity with SEQ ID NO: 55, and wherein the polypeptide has permease activity.
摘要翻译: 本发明涉及在一个或多个对应于SEQ ID NO:55的T219的位置具有突变的多肽,其中多肽与SEQ ID NO:55具有至少50%的序列同一性,并且其中多肽具有通透酶活性。
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