摘要:
The invention relates to an isolated polynucleotide having a polynucleotide sequence which codes for the alr gene, and a host-vector system having a coryneform host bacterium in which the alr gene is present in attenuated form and a vector which carries at least the alr gene according to SEQ ID No 1, and the use of polynucleotides which comprise the sequences according to the invention as hybridization probes.
摘要翻译:本发明涉及具有编码alr基因的多核苷酸序列的分离的多核苷酸,以及具有其中alr基因以减毒形式存在的棒状细胞宿主细菌的宿主 - 载体系统和至少携带alr基因的载体 至SEQ ID No 1,以及使用包含根据本发明的序列的多核苷酸作为杂交探针。
摘要:
This invention relates to the mutually compatible plasmids pTET3 and pCRY4, isolated from the strain of Corynebacterium glutamicum deposited under DSM number 5616, wherein plasmid pTET3 is characterised by 1.1 a length of ˜27.8 kbp and the restriction map shown in FIG. 1, 1.2 a replication region comprising the nucleotide sequence shown in SEQ ID no. 1 and 1.3 an antibiotic resistance region consisting of a tetA gene imparting tetracycline resistance and an aadA gene imparting streptomycin and spectinomycin resistance, shown in SEQ ID no. 6, and plasmid pCRY4 is characterised by 1.4 a length of ˜48 kbp and the restriction map shown in FIG. 2 and 1.5 a replication region comprising the nucleotide sequence shown in SEQ ID no. 4 to composite plasmid vectors of these plasmids which are capable of autonomous replication in coryneform bacteria and to processes for the production of L-amino acids, vitamins and nucleotides using these bacteria.
摘要翻译:本发明涉及从DSM号5616中沉积的谷氨酸棒杆菌菌株分离的相互相容的质粒pTET3和pCRY4,其中质粒pTET3的特征在于1.1,长度为约27.8kbp,图1所示的限制性图谱。 1,1.2复制区,其包含SEQ ID No: 1和1.3由SEQ ID No.3所示的赋予四环素抗性的tetA基因和赋予链霉素和壮观霉素抗性的aadA基因组成的抗生素抗性区域。 6,并且质粒pCRY4的特征在于1.4〜48kbp的长度以及图4所示的限制性图谱。 2和1.5复制区,其包含SEQ ID No: 这些质粒能够在棒状细菌中自主复制的这些质粒的复合质粒载体和使用这些细菌生产L-氨基酸,维生素和核苷酸的方法。
摘要:
A method for the production of D-pantothenic acid by the fermentation of microorganisms of the family Enterobacteriacae producing D-pantothenic acid which is characterized in that strains are used which a) Contain the plasmid pFV31 and/or pFV202 and that b) A panD gene and optionally other nucleotide sequences coding for aspartate-1-decarboxylase are enhanced, especially overexpressed in these microorganisms, c) The pantothenic acid is enriched in the medium or in the cells of the microorganisms and d) The pantothenic acid formed is isolated.
摘要:
The invention relates to a process for the preparation and improvement of D-pantothenic acid-producing microorganisms by amplification of nucleotide sequences which code for ketopantoate reductase, in particular the panE gene, individually or in combination with one another, and optionally additionally of the ilvC gene, the microorganisms containing these nucleotide sequences, and a process for the preparation of D-pantothenic acid comprising fermentation of these microorganisms, concentration of pantothenic acid in the medium or in the cells of the microorganisms, and isolation of the D-pantothenic acid.
摘要:
The invention relates to a process for the preparation and improvement of D-pantothenic acid-producing microorganisms by amplification of nucleotide sequences which code for ketopantoate reductase, in particular the panE gene, individually or in combination with one another, and optionally additionally of the ilvC gene, the microorganisms containing these nucleotide sequences, and a process for the preparation of D-pantothenic acid comprising fermentation of these microorganisms, concentration of pantothenic acid in the medium or in the cells of the microorganisms, and isolation of the D-pantothenic acid.
摘要:
An isolated polynucleotide containing a polynucleotide sequence selected from the group a) polynucleotide which is at least 70% identical to a polynucleotide which codes for a polypeptide containing the amino acid sequence of SEQ ID no. 2, b) polynucleotide which codes for a polypeptide which contains an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID no. 2, c) polynucleotide which is complementary to the polynucleotides of a) or b) and d) polynucleotide containing at least 15 successive bases of the polynucleotide sequence of a), b) or c), and a process for the fermentative production of L-amino acids by attenuation of the poxB gene.
摘要翻译:一种分离的多核苷酸,其含有多核苷酸序列,所述多核苷酸序列选自a)多核苷酸,其与编码含有SEQ ID NO:1的氨基酸序列的多肽的多核苷酸至少70%相同。 2,b)编码多肽的多核苷酸,其含有与SEQ ID No:1的氨基酸序列至少70%相同的氨基酸序列。 2)c)与a)或b)的多核苷酸互补的多核苷酸,和d)包含a),b)或c)多核苷酸序列的至少15个连续碱基的多核苷酸,以及发酵生产L - 氨基酸通过减少poxB基因。
摘要:
The invention relates to an isolated polynucleotide from coryneform bacteria containing at least one polynucleotide sequence selected from the group consisting of a) polynucleotide which is at least 70% identical to a polynucleotide which encodes a polypeptide containing the amino acid sequence according to SEQ ID no. 2, b) polynucleotide which encodes a polypeptide which contains an amino acid sequence which is at least 70% identical to the amino acid sequence of SEQ ID no. 2, c) polynucleotide which is complementary to the polynucleotides of a) or b), and d) polynucleotide containing at least 15 successive nucleotides of the polynucleotide sequences of a), b) or c), and to a process for the fermentative production of L-amino acids, in particular L-lysine.
摘要翻译:本发明涉及来自棒状细菌的分离的多核苷酸,其含有至少一种多核苷酸序列,所述多核苷酸序列选自a)多核苷酸,其与编码含有根据SEQ ID No.3所述的氨基酸序列的多肽的多核苷酸至少70%相同。 2,b)编码多肽的多核苷酸,其含有与SEQ ID NO:1的氨基酸序列至少70%相同的氨基酸序列。 2)c)与a)或b)的多核苷酸互补的多核苷酸,和d)包含a),b)或c)的多核苷酸序列的至少15个连续核苷酸的多核苷酸,以及d)发酵生产的方法 的L-氨基酸,特别是L-赖氨酸。
摘要:
Disclosed herein is an isolated polynucleotide comprising a polynucleotide sequence chosen from the group consisting of a) polynucleotide which is identical to the extent of at least 70% to a polynucleotide which codes for a polypeptide which comprises the amino acid sequence of SEQ ID NO:2, b) polynucleotide which codes for a polypeptide which comprises an amino acid sequence which is identical to the extent of at least 70% to the amino acid sequence of SEQ ID NO:2 c) polynucleotide which is complementary to the polynucleotides of a) and b) and d) polynucleotide comprising at least 15 successive nucleotides of the polynucleotide sequence of a), b) or c), and processes for the fermentative preparation of L-amino acid with amplification of the zwa1 gene in the coryneform bacteria employed.
摘要翻译:本文公开了一种分离的多核苷酸,其包含选自以下的多核苷酸序列:a)与编码包含SEQ ID NO:2的氨基酸序列的多肽的多核苷酸的程度相同的多核苷酸 b)编码多肽的多核苷酸,其包含与SEQ ID NO:2的氨基酸序列至少70%相同程度的氨基酸序列c)与a)和 b)和d)包含a),b)或c)的多核苷酸序列的至少15个连续核苷酸的多核苷酸,以及在所用棒状细菌中扩增zwa1基因的L-氨基酸的发酵制剂的方法。
摘要:
The present invention relates to a method of effecting the conjugative transfer of a mobilizable vector from cells of an E. coli mobilizer strain to gram-positive bacterial cells. The invention also relates to vectors suitable for use in such a method.
摘要:
The invention relates to a transposon consisting of a fragment of the R plasmid pCxM82B from Corynebacterium xerosis DSM 5021, to mobilizable, non-self-transferrable vectors which contain this transposon, and to methods for the mutagenesis of gram-positive bacteria by means of the transfer of these vectors and the generation of auxotrophic mutants.