首页> 外国专利> DNA SEQUENCES FOR 5S CLAVAM BIOSYNTHESIS IN STREPTOMYCES CLAVULIGERUS MICROORGANISMS, STREPTOMYCES CLAVULIGERUS MICROORGANISM STRAINS, CONTAINING SAID DNA SEQUENCES AND A PROCESS FOR IMPROVING 5R CLAVAM PRODUCTION, IN PARTICULAR, CLAVULANIC ACID IN STREPTOMYCES CLAVULIGERUS MICROORGANISMS

DNA SEQUENCES FOR 5S CLAVAM BIOSYNTHESIS IN STREPTOMYCES CLAVULIGERUS MICROORGANISMS, STREPTOMYCES CLAVULIGERUS MICROORGANISM STRAINS, CONTAINING SAID DNA SEQUENCES AND A PROCESS FOR IMPROVING 5R CLAVAM PRODUCTION, IN PARTICULAR, CLAVULANIC ACID IN STREPTOMYCES CLAVULIGERUS MICROORGANISMS

机译:链霉菌克拉维奇菌微生物,链霉菌克拉维奇菌微生物菌株中5S克拉维菌生物合成的DNA序列,包含有用的DNA序列,以及特别是在蟹形细菌中,提高5R克拉维霉菌产量的过程

摘要

1. A DNA molecule comprising a cas1 gene and flanking regions specific for 5S clavam biosynthesis in Streptomyces clavuligerus microorganisms and which is not essential for 5R clavam biosynthesis having nucleid sequence (SEQ ID No. 1), identified in Figure 1 or a DNA molecule which is hybridised under conditions of high stringency with said DHA molecule. 2. The DNA molecule which is an open reading frame specific for 5S clavam biosynthesis in Streptomyces clavuligerus microorganisms and which is not essential for 5R clavam biosynthesis selected from the group consisting of: a). orfup1, having the sequence (SEQ ID No. 4); b). orfup2, having the sequence (SEQ ID No. 3); c). orfup3, having the sequence (SEQ ID No. 2); d). orfdwn1, having the sequence (SEQ ID No. 5); e). orfdwn2, having the sequence (SEQ ID No. 6); f). orfdwn3, having the sequence (SEQ ID No. 7). 3. A vector comprising the DNA molecule of any one of claims 1 or 2. 4. Plasmid comprising one or more genes specific for 5S clavam biosynthesis from which one or more genes has been disrupted or otherwise made defective wherein the genes correspond to open reading frame selected from the group consisting of: a). orfup1, having the sequence (SEQ ID No. 4); b). orfup2, having the sequence (SEQ ID No. 3); c). orfup3, having the sequence (SEQ ID No. 2); d). orfdwn1, having the sequence (SEQ ID No. 5); e). orfdwn2, having the sequence (SEQ ID No. 6); f). orfdwn3, having the sequence (SEQ ID No. 7). 5. The plasmid of claim 4 which is pCEC060, pCEC061, pCEC056, pCEC057 or pDES3. 6. Streptomyces clavuligerus microorganism strain comprising the plasmid of claim 4. 7. Streptomyces clavuligerus microorganism strain comprising one or more genes specific for 5S clavam biosynthesis from which one or more genes has been disrupted or otherwise made defective wherein the genes have open reading frame selected from the group consisting of: a). orfup1, having the sequence (SEQ ID No. 4); b). orfup2, having the sequence (SEQ ID No. 3); c). orfup3, having the sequence (SEQ ID No. 2); d). orfdwn1, having the sequence (SEQ ID No. 5); e). orfdwn2, having the sequence (SEQ ID No. 6); f). orfdwn3, having the sequence (SEQ ID No. 7); wherein said disrupted or otherwise made defective genes have been included in said Streptomyces clavuligerus microorganism strain by changing genes using the plasmid of claim 4. 8. A process for improving 5R clavam production in a Streptomyces clavuligerus microorganism strain comprising the steps of: a). disrupting or otherwise making defective DNA of claim 1 or 2; b). introducing disrupted or defective DNA obtained after a) in Streptomyces clavuligerus microorganism strain capable of producing 5R clavam; and c). fermentation of Streptomyces clavuligerus microorganism strain obtained after b) under conditions suitable for producing 5R clavam. 9. The process of claim 8, wherein said DNA corresponds to open reading frames ortup3, ortup2, orfupl, orfdwn 1, orfdwn2 or orfdwn3. 10. The process of claim 8 or 9, wherein the 5R clavam is clavulanic acid.
机译:1.一种DNA分子,该DNA分子包含cas1基因和特异于棒状链霉菌微生物中5S克拉维生物合成的侧翼区,并且对于图1所示的具有核序列(SEQ ID No.1)的5R克拉维生物合成不是必需的,或在高度严格的条件下将其与所述DHA分子杂交。 2.DNA分子,其是对链霉菌微生物中的5S克拉维生物合成具有特异性的开放阅读框,并且对于选自以下的5R克拉维生物合成而言不是必需的:a)。 orfup1,具有序列(SEQ ID No. 4); b)。 orfup2,具有序列(SEQ ID No.3); C)。 orfup3,具有序列(SEQ ID No.2); d)。 orfdwn1,具有序列(SEQ ID No. 5); e)。 orfdwn2,具有序列(SEQ ID No. 6); F)。 orfdwn3,具有序列(SEQ ID No. 7)。 3.一种载体,其包含权利要求1或2中任一项的DNA分子。4.质粒,其包含一个或多个对5S克拉维生物合成具有特异性的基因,其中一个或多个基因已被破坏或以其他方式使其有缺陷,其中所述基因对应于开放阅读框架选自:a)。 orfup1,具有序列(SEQ ID No. 4); b)。 orfup2,具有序列(SEQ ID No.3); C)。 orfup3,具有序列(SEQ ID No.2); d)。 orfdwn1,具有序列(SEQ ID No. 5); e)。 orfdwn2,具有序列(SEQ ID No. 6); F)。 orfdwn3,具有序列(SEQ ID No. 7)。 5.权利要求4的质粒,其是pCEC060,pCEC061,pCEC056,pCEC057或pDES3。 6.包含权利要求4的质粒的棒状链霉菌微生物菌株。7.包含对5S克拉维生物合成特异的一种或多种基因的链霉菌棒状微生物微生物菌株,从中破坏了一个或多个基因或使其具有缺陷,其中所述基因具有选择的开放阅读框选自:a)。 orfup1,具有序列(SEQ ID No. 4); b)。 orfup2,具有序列(SEQ ID No.3); C)。 orfup3,具有序列(SEQ ID No.2); d)。 orfdwn1,具有序列(SEQ ID No. 5); e)。 orfdwn2,具有序列(SEQ ID No. 6); F)。 orfdwn3,具有序列(SEQ ID No. 7);其中通过使用权利要求4的质粒通过改变基因,将所述破坏的或以其他方式产生的缺陷基因包括在所述锁链霉菌微生物菌株中。8.一种用于改善在锁链霉菌微生物菌株中5R克拉瓦生产的方法,该方法包括以下步骤:a)。破坏或以其他方式制造权利要求1或2的缺陷DNA; b)。将在a)之后获得的破坏的或有缺陷的DNA导入能够产生5R克拉维的克拉维链霉菌微生物菌株中;和c)。 b)在适于产生5R克拉瓦姆的条件下,发酵b)后获得的棒状链霉菌微生物菌株。 9.权利要求8的方法,其中所述DNA对应于开放阅读框ortup3,ortup2,orfupl,orfdwn 1,orfdwn2或orfdwn3。 10.根据权利要求8或9所述的方法,其中所述5R克拉维姆为克拉维酸。

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