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A soybean gene encoding Δ1-pyrroline-5-carboxylate reductase was isolated by functional complementation in Escherichia coli and is found to be osmoregulated

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Summary

We have isolated several cDNA clones encoding Δ1 1-pyrroline-5-carboxylate reductase (P5CR, l-proline: NAD(P)+ 5-oxidoreductase, EC 1.5.1.2) which catalyzes the terminal step in proline biosynthesis, by direct complementation of a proC mutation in Escherichia coli with an expression library of soybean root nodule cDNA. The library was constructed in the λ ZapII vector, converted to a plasmid library by in vivo excision of recombinant pBluescript phagemids, and used for transformation of the E. coli mutant. Complementing plasmids contained inserts of about 1.2 kb which hybridized to a 1.3 kb RNA transcript in nodules, uninfected roots and leaves. DNA sequence analysis of one full length cDNA clone showed that it encoded a 28 586 Mr polypeptide with 39% amino acid identity to the E. coli P5CR sequence. Genomic analysis showed that there are two to three copies of the P5CR gene in the soybean genome. The steady-state level of P5CR mRNA in root nodules was twice as high as in uninfected roots and about five times higher than in leaves. Subjecting young seedlings to osmotic stress by watering with 400 mM NaCl resulted in an almost six-fold increase in the level of root P5CR mRNA, suggesting that this gene may be osmoregulated.

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References

  • Adams E, Frank L (1980) Metabolism of proline and the hydroxyprolines. Annu Rev Biochem 49:1005–1061

    Google Scholar 

  • Ausubel FM, Brent R, Kingston RE, Moore DD, Smith JA, Seidman JG, Struhl K (1987) Current Protocols in Molecular Biology. Green/Wiley Interscience, New York, p 1.1.2

    Google Scholar 

  • Bachmann BJ (1987) Linkage map of Escherichia coli K-12, edition 7. In: Neidhardt FC, Ingraham JL, Low KB, Magasanik B, Schaechter M, Umbarger HE (eds) Escherichia coli and Salmonella typhimurium Cellular and Molecular Biology. American Society for Microbiology, Washington, DC, pp 807–876

    Google Scholar 

  • Bernard T, Pocard J-A, Perroud B, LeRudulier D (1982) Variations in response of salt-stressed Rhizobium strains to betaines. Arch Microbiol 143:359–364

    Google Scholar 

  • Csonka LN (1989) Physiological and genetic responses of bacteria to osmotic stress. Microbiol Rev 53:121–147

    Google Scholar 

  • DasSarma S, Tischer E, Goodman HM (1986) Plant glutamine synthetase complements a glnA mutation in Escherichia coli. Science 232:1242–1244

    Google Scholar 

  • Delauney AJ, Tabaeizadeh Z, Verma DPS (1988) A stable bifunctional antisense transcript inhibiting gene expression in transgenic plants. Proc Natl Acad Sci USA 85:4300–4304

    Google Scholar 

  • Deutch AH, Smith CJ, Rushlow KE, Kretschmer PJ (1982) Analysis of the Escherichia coli proBA locus by DNA and protein sequencing. Nucleic Acids Res 10: 7701–7714

    Google Scholar 

  • Gubler U, Hoffman BJ (1983) A simple and very efficient method for generating cDNA libraries. Gene 25:263–269

    Google Scholar 

  • Hanahan D (1985) Techniques for transformation of E. coli. In: Glover DM (ed) DNA Cloning: A Practical Approach, vol. I. IRL Press, Oxford, pp 109–135

    Google Scholar 

  • Jones JDG, Dunsmuir P, Bedbrook J (1985) High level expression of introduced chimaeric genes in regenerated transformed plants. EMBO J 4:2411–2418

    CAS  Google Scholar 

  • Kohl DH, Schubert KR, Carter MB, Hagedorn CH, Shearer G (1988) Proline metabolism in N2-fixing root nodules: energy transfer and regulation of synthesis. Proc Natl Acad Sci USA 85:2036–2040

    Google Scholar 

  • Larsen PI, Sydnes LK, Landfald B, Strom AR (1987) Osmoregulation in Escherichia coli by accumulation of organic osmolytes: betaines, glutamic acid, and trehalose. Arch Microbiol 147:1–7

    Google Scholar 

  • Leisinger T (1987) Biosynthesis of proline. In: Neidhardt FC, Ingraham JL, Low KB, Magasanik B, Schaechter M, Umbarger HE (eds) Escherichia coli and Salmonella typhimurium Cellular and Molecular Biology. American Society for Microbiology, Washington, DC, pp 345–351

    Google Scholar 

  • Le Rudulier D, Young SS, Csonka LN (1982) Nitrogen fixation in Klebsiella pneumoniae during osmotic stress: effect of oxygenous proline overproducing plasmid. Biochim Biophys Acta 719:273–283

    Google Scholar 

  • Le Rudulier D, Strom AM, Dandekar AM, Smith LT, Valentine RC (1984) Molecular biology of osmoregulation. Science 224:1064–1068

    CAS  Google Scholar 

  • Mahmoudi M, Lin VK (1989) Comparison of two different hybridization systems in northern transfer analysis. Biotechniques 7:331–333

    Google Scholar 

  • Matthews BF, Reardon EM, Turano FJ, Wilson BJ (1988) Amino acid biosynthesis in plants — approaching an understanding at the molecular level. Plant Mol Biol Rep 6:137–154

    Google Scholar 

  • McCabe DE, Swain WF, Martinell BJ, Christou P (1988) Stable transformation of soybean (Glycine max.) by particle acceleration. Bio/Technology 6:923–926

    Google Scholar 

  • Schubert KR (1986) Products of biological nitrogen fixation in higher plants: synthesis, transport, and metabolism. Annu Rev Plant Physiol 37:539–574

    Google Scholar 

  • Shiono T, Kador PF, Kinoshita JJ (1986) Purification and characterization of rat lens pyrroline-5-carboxylate reductase. Biochim Biophys Acta 881:72–78

    Google Scholar 

  • Snustad DP, Hunsperger JP, Chereskin BM, Messing J (1988) Maize glutamine synthetase cDNAs: isolation by direct genetic selection in Escherichia coli. Genetics 120:1111–1124

    Google Scholar 

  • Steege DA (1977) 5′-terminal nucleotides sequence of Escherichia coli lactose repressor mRNA: features of transitional initiation and reinitiation sites. Proc Natl Acad Sci USA 74:4163–4167

    Google Scholar 

  • Stewart CR (1981) Proline accumulation: biochemical aspects. In: Beleg LG, Espinall D (eds) Physiology and Biochemistry of Drought Resistance in Plants. Academic Press, Sydney, Australia, pp 243–259

    Google Scholar 

  • Streeter JG (1985) Accumulation of α, α-trehalose by Rhizobium bacteria and bacteroids. J Bacteriol 164:78–84

    Google Scholar 

  • Thompson JF (1980) Arginine synthesis, proline synthesis, and related processes. In: Miflin BJ (ed) The Biochemistry of Plants, vol 5: Amino Acids and Derivatives. Academic Press, New York, pp 375–402

    Google Scholar 

  • Tomenchok DM, Brandriss MA (1987) Gene-enzyme relationships in the proline biosynthetic pathway of Saccharamyces cerevisiae. J Bacteriol 169:5364–5372

    Google Scholar 

  • Treichel S (1986) The influence of NaCl on Δ1-pyrroline-carboxylate reductase in proline-accumulating cell suspension cultures of Mesembryanthemum nodiflorum and other halophytes. Physiol Plant 67:173–181

    Google Scholar 

  • Verma DPS, Delauney AJ (1988) Root nodule symbiosis: nodulins and nodulin genes. In: Verma DPS, Goldberg R (eds) Temporal and Spatial Regulation of Plant Genes. Springer-Verlag, New York, pp 169–199

    Google Scholar 

  • Verma DPS, Kazazian V, Zogbi V, Bal AK (1978) Isolation and characterization of the membrane envelope enclosing the bacteroids in soybean root nodules. J Cell Biol 78:919–936

    Google Scholar 

  • Verma DPS, Fortin MG, Stanley J, Mauro VP, Purohit S, Morrison N (1986) Nodulins and nodulin genes of Glycine max. Plant Mol Biol 7:51–61

    Google Scholar 

  • Wong S-L, Verma DPS (1985) Promoter analysis of a soybean nuclear gene coding for nodulin-23, a nodule-specific polypeptide involved with symbiosis with Rhizobium. EMBO J 4:2431–2438

    Google Scholar 

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Communicated by H. Hennecke

EMBL Accession number: X16352

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Delauney, A.J., Verma, D.P.S. A soybean gene encoding Δ1-pyrroline-5-carboxylate reductase was isolated by functional complementation in Escherichia coli and is found to be osmoregulated. Mol Gen Genet 221, 299–305 (1990). https://doi.org/10.1007/BF00259392

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  • DOI: https://doi.org/10.1007/BF00259392

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