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General organization of the genes specifically involved in the diaminopimelate-lysine biosynthetic pathway of Corynebacterium glutamicum

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Summary

We utilized diaminopimelate-lysine mutants of Escherichia coli K12 to clone the genes specifically involved in the Corynebacterium glutamicum diaminopimelate-lysine anabolic pathway. From a cosmid genomic bank of C. glutamicum strain AS019, we isolated cosmids pSM71, pSM61 and pSM531, that are respectively able to complement dapA/dapB, dapD, and lysA mutants of E. coli. DNA hybridization analysis indicates that these complementing genes are located on the chromosome of C. glutamicum in at least three separate transcription units. Subcloning of parental cosmids in dapA, dapD, and lysA mutants of E. coli localized these genes, respectively, within 1.4, 3.4, and 1.8 kb fragments, cloned in an E. coli/C. glutamicum shuttle vector. Enzymatic analysis in C. glutamicum identified the dapA-complementing gene as l-2,3-dihydrodipicolinate synthetase (dapA), and the lysA-complementing gene as meso-diaminopimelate decarboxylase (lysA). In contrast, complementation of E. coli dapD8, presumably lacking L-Δ1-tetrahydrodipicolinate synthetase (dapD), led us to clone a diaminopimelate-lysine anabolic gene of C. glutamicum which does not exist in E. coli: meso-diaminopimelate dehydrogenase. Although meso-diaminopimelate is crucial in lysine formation and in cell wall biosynthesis, expression of the genomic copies of the cloned genes, which encode activities involved at key branching points of the diaminopimelate-lysine pathway of C. glutamicum, appears constitutive with regard to the addition of diaminopimelate and/or lysine during cell growth.

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References

  • Annie T, Bartlett M, White PJ (1985) Species of bacillus that make a vegetative peptidoglycan containing lysine lack diaminopimelate epimerase but have diaminopimelate dehydrogenase. J Gen Microbiol 131:2145–2152

    Google Scholar 

  • Bachmann B (1983) Linkage map of Escherichia coli K-12. Ed. 7, Microbiol Rev 47:180–230

    Google Scholar 

  • Batt CA, Follettie MT, Shin HK, Yeh P, Sinskey AJ (1985) Genetic engineering of coryneform bacteria. Trends Biotechnol 3:305–310

    Google Scholar 

  • Birnboim HC, Doly J (1979) A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res 7:1513–1523

    Google Scholar 

  • Bouvier J, Richaud C, Richaud F, Patte JC, Stragier P (1984) Nucleotide sequence and expression of the E. coli dapB gene. J Biol Chem 259:14829–14834

    Google Scholar 

  • Boy E, Richaud C, Patte JC (1979) Multiple regulation of DAP-decarboxylase synthesis in E. coli K-12. FEMS Microbiol Lett 5:287–290

    Google Scholar 

  • Bukhari AI, Taylor AL (1971a) Genetic analysis diaminopimelic acid- and lysine-requiring mutants of Escherichia coli. J Bacteriol 105:844–854

    Google Scholar 

  • Bukhari AI, Taylor AL (1971b) Mutants of Escherichia coli with a growth requirement for either lysine or pyridoxine. J Bacteriol 105:988–998

    Google Scholar 

  • Cohen SN, Chang ACY, Hsu L (1973) Nonchromosomal antibiotic resistance in bacteria: genetic transformation of Escherichia coli by R-factor DNA. Proc Natl Acad Sci USA 69:2110–2114

    Google Scholar 

  • Del Real G, Aguilar A, Martin JF (1985) Cloning and expression of tryptophan genes from Brevibacterium lactofermentum in Escherichia coli. Biochem Biophys Res Commun 133:1013–1019

    Google Scholar 

  • Follettie MT, Sinskey AJ (1986) Molecular cloning and nucleotide sequence of the C. glutamicum pheA gene. J Bacteriol 167:695–702

    Google Scholar 

  • Ishino S, Yamaguchi K, Shirahata K, Araki K (1984) Involvement of meso-α,ε-diaminopimelate d-dehydrogenase in lysine biosynthesis in C. glutamicum. Agric Biol Chem 48:2557–2560

    Google Scholar 

  • Keddie RM, Cure GL (1978) Cell wall composition. In: Bousfield IJ, Callaly AG (eds) Coryneform bacteria. Academic Press Inc., London, pp 47–83

    Google Scholar 

  • Kelland JG, Palcic MM, Pickard MA, Vederas JC (1985) Stereochemistry of lysine formation by meso-diaminopimelate decarboxylase from wheat germ: use of 1H−13C NMR shift correlation to detect stereospecific deuterium labelling. Biochemistry 24:3263–3267

    Google Scholar 

  • Maniatis T, Fritsch FF, Sambrook J (1982) Molecular cloning, a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Marquez G, Fernandez Sousa JM, Sanchez F (1985) Cloning and expression in E. coli of genes involved in the lysine pathway of B. lactofermentum. J Bacteriol 164:379–383

    Google Scholar 

  • Martin C, Borne F, Cami B, Patte JC (1986) Autogenous regulation by lysine of the lysA gene of Escherichia coli. FEMS Microbiol Lett 36:105–108

    Google Scholar 

  • Mateos LM, Del Real G, Aguilar A, Martin JF (1987) Cloning and expression in Escherichia coli of the homoserine kinase (thrB) gene from Brevibacterium lactofermentum. Mol Gen Genet 206:361–367

    Google Scholar 

  • Minnikin DE, Goodfellow M, Collins MD (1978) Lipid composition in the classification and identification of coryneform and related taxa. In: Bousfield IJ, Callaly AG (eds) Coryneform bacteria. Academic Press, London, pp 85–160

    Google Scholar 

  • Misono H, Togawa H, Yamamoto T, Soda K (1979) Meso-α,ε-diaminopimelate d-dehydrogenase: distribution and the reaction product. J Bacteriol 137:22–27

    Google Scholar 

  • Ozaki A, Katsumata R, Oka T, Furuya A (1985) Cloning of the genes concerned in phenylalanine biosynthesis in Corynebacterium glutamicum and its application to breeding of a phenylalanine-producing strain. Agric Biol Chem 49:2925–2930

    Google Scholar 

  • Patte JC (1983) Diaminopimelate and lysine. In: Hermann K, Somerville R (eds) Amino acid biosynthesis and genetic regulation. Addison-Wesley Publishing Co., Reading, MA

    Google Scholar 

  • Pitcher DG (1983) Deoxyribonucleic acid base composition of Corynebacterium diphtheriae and corynebacteria with cell wall type IV. FEMS Microbiol Lett 16:291–295

    Google Scholar 

  • Richaud C, Richaud F, Martin C, Haziza C, Patte JC (1984) Regulation of expression and nucleotide sequence of the E. coli dapD gene. J Biol Chem 259:14824–14828

    Google Scholar 

  • Richaud C, Higgins W, Mengin-Lecreulx D, Stragier P (1987) Molecular cloning, characterization, and chromosomal localization of dapF, the Escherichia coli gene for diaminopimelate epimerase. J Bacteriol 169:1454–1459

    Google Scholar 

  • Richaud F, Richaud C, Ratet P, Patte JC (1986) Chromosmal location and nucleotide sequence of the E. coli dapA gene. J Bacteriol 166:297–300

    Google Scholar 

  • Rigby PW, Dieckmann M, Rhodes C, Berg P (1977) Labelling DNA to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol 113:237–251

    Google Scholar 

  • Shiio I, Miyajima R (1969) Concerted inhibition and its reversal by end products of aspartate kinase in Brevibacterium flavum. J Biochem 65:849–859

    Google Scholar 

  • Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–517

    Google Scholar 

  • Stragier P, Patte JC (1983) Regulation of diaminopimelate decarboxylase synthesis in E. coli: III. Nucleotide sequence and regulation of the lysR gene. J Mol Biol 168:333–350

    Google Scholar 

  • Stragier P, Richaud F, Borne F, Patte JC (1983a) Regulation of diaminopimelate decarboxylase synthesis in E. coli: I. Identification of a lysR gene encoding an activator of the lysA gene. J Mol Biol 168:307–320

    Google Scholar 

  • Stragier P, Danos O, Patte JC (1983b) Regulation of diaminopimelate decarboxylase synthesis in E. coli: II. Nucleotide sequence of the lysA gene and its regulatory region. J Mol Biol 168:321–331

    Google Scholar 

  • Tosaka O, Takinami K (1978) Pathway and regulation of lysine biosynthesis in Brevibacterium lactofermentum. Agric Biol Chem 42:95–100

    Google Scholar 

  • Tosaka O, Hirakawa H, Takinami K, Hirose Y (1978) Regulation of lysine biosynthesis by leucine in Brevibacterium lactofermentum. Agric Biol Chem 42:1501–1506

    Google Scholar 

  • Vieira J, Messing J (1982) The pUC plasmids, an M13 mp7 derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene 19:259–268

    Google Scholar 

  • Yeh P, Sicard AM, Sinskey AJ (1988) Nucleotide sequence of the lysA gene of Corynebacterium glutamicum and possible mechanisms for modulation of its expression. Mol Gen Genet 212:112–119

    Google Scholar 

  • Yoshihama M, Higashino K, Eswara AR, Akedo M, Shanabrush WG, Follettie MT, Walker GC, Sinskey AJ (1985) Cloning vector system for Corynebacterium glutamicum. J Bacteriol 162:591–597

    Google Scholar 

  • Yugari Y, Gilvarg C (1965) The condensation step in diaminopimelate synthesis. J Biol Chem 240:4710–4716

    Google Scholar 

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Communicated by J.W. Lengeler

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Yeh, P., Sicard, A.M. & Sinskey, A.J. General organization of the genes specifically involved in the diaminopimelate-lysine biosynthetic pathway of Corynebacterium glutamicum . Molec. Gen. Genet. 212, 105–111 (1988). https://doi.org/10.1007/BF00322451

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