Process for the preparation of l-amino acids using strains of the enterobacteriaceae family
A technology of Enterobacteriaceae and amino acids, applied in the field of L-threonine and microorganisms, can solve the problem of undetectable
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Embodiment 1
[0156] Example 1: Construction of expression plasmid pTrc99AmalT
[0157] The malT gene of E. coli K12 was amplified using polymerase chain reaction (PCR) and synthetic oligonucleotides. Starting from the nucleotide sequence of the malT gene of E. coli K12 MG1655 (Accession No. AE000418, Blattner et al. (Science 277: 1453-1474 (1997)), PCR primers were synthesized (MWG Biotech, Ebersberg, Germany). The primers contain sequences of restriction enzymes, which are underlined in the nucleotide sequences shown below.Primer malT1 contains a restriction cleavage site for XabI, and primer malT2 contains a restriction cleavage site for HindIII.
[0158] malT1:
[0159] 5′-CCTCAT TCTAG ACAGTGAAGTGATTAA-3' (SEQ ID No: 1)
[0160] malT2:
[0161] 5′-GGCGCGTTATC AAGCTT AACTTACAC-3' (SEQ ID No: 2)
[0162] Chromosomal DNA of E. coli K12 MG1655 for PCR was isolated using Qiagen Genomic-tips 100 / G (QIAGEN, Hilden, Germany) according to the manufacturer's instructions. Using specific p...
Embodiment 2
[0164] Example 2: Preparation of L-threonine with bacterial strain MG442 / pTrc99AmalT
[0165] The Escherichia coli strain MG442 producing L-threonine is described in patent specification US-A-4,278,765, deposited with the Russian State Collection of Industrial Microorganisms (VKPM, Moscow, Russia) under the Budapest Treaty under the deposit number CMIM B-1628 and with the deposit number DSM 16574 is deposited at the German Collection of Microorganisms (DSMZ, Braunschweig, Germany).
[0166]Strain MG442 was transformed with the expression plasmid pTrc99AmalT and the vector pTrc99A described in Example 1, and cells carrying the plasmids were selected on LB agar with 50 μg / ml ampicillin. Successful transformation was confirmed by control cleavage with the enzymes HpaI, HindIII / XbaI and EcoRV after isolation of the plasmid DNA. In this way the strains MG442 / pTrc99AmalT and MG442 / pTrc99A were formed. Selected individual colonies were then further propagated on minimal medium with...
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