Skip to main content
Log in

Use of NaCN to increase the growth of N2-fixing bacteria in a model spermosphere mimicked by sucrose and amino acids leached by seeds

  • Original Paper
  • Published:
Biology and Fertility of Soils Aims and scope Submit manuscript

Abstract

In order to study the establishment of a spermosphere, the C2H2 reduction activity of N2-fixing bacteria isolated from river sand was examined in a simulated spermosphere in the river sand which contained sucrose, an amino acid mixture, and CN- released from plant seeds. The sand incubated with 10-10 to 10-9 mol CN- 30 g sand-1 exhibited higher C2H2 reduction activity than that without CN-. The change in the most probable number of N2 fixers with increasing quantities of CN- roughly corresponded to that in C2H2 reduction activity. However, the most probable number of non-N2-fixing bacteria decreased except for CN--tolerant ones. Both C2H2 reduction activity and proliferation of the N2 fixers isolated on a modified Burk's medium were almost similar to those in the bacteria in the sand. In contrast, the proliferation of some nonfixers decreased with an increasing CN- concentration. C2H2 reduction activity of N2 fixers cultured in combination with non-fixers exhibited a clear peak at 10-7 M CN- as for C2H2 reduction activity in the sand. We therefore speculate that cyanide evolved from seeds during a pregermination period may suppress the growth of general bacteria, but may promote the proliferation of N2 fixers, thus contributing to the establishment of a spermosphere.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Abbot TP, Nakamura LK, Nelsen TC, Gasdorf HJ, Bennett GA, Kleiman R (1990) Microorganisms for degrading simmondsin and related cyanogenic toxins in jojoba. Appl Microbiol Biotechnol 34:270–273

    Google Scholar 

  • van Berkum P, Sloger C (1979) Immediate acetylene reduction by excised grass root not previously preincubated at low oxygen tensions. Plant Physiol 64:739–743

    Google Scholar 

  • Conn EE (1980) Cyanogenic compounds. Annu Rev Plant Physiol 31:433–451

    Google Scholar 

  • Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356

    Google Scholar 

  • Esashi Y, Isuzugawa K, Matsuyama S, Ashino H, Hasegawa R (1991) Endogenous evolution of HCN during pre-germination periods in many seed species. Physiol Plant 83:27–33

    Google Scholar 

  • Harris R, Knowles CJ (1983) Isolation and growth of a Pseudomonas species that utilizes cyanide as a source of nitrogen. J Gen Microbiol 129:1005–1011

    Google Scholar 

  • Hwang JC, Burris RH (1972) Nitrogenase-catalyzed reaction. Biochim Biophys Acta 283:339–350

    Google Scholar 

  • Li J-G, Burgess BK, Corbin JL (1982) Nitrogenase-reactivity: Cyanide as substrate and inhibitor. Biochem 21:4393–4402

    Google Scholar 

  • Lowe DJ, Fisher K, Thorneley RNF, Vaughn SA, Burgess BK (1989) Kinetics and mechanism of the reaction of cyanide with molybdenum nitrogenase from Azotobacter vinelandii. Biochem 28:8460–8466

    Google Scholar 

  • Nawaz MS, Davis JW, Wolfram JH, Chapatwala KD (1991) Degradation of organic cyanides by Pseudomonas aeruginosa. Appl Biochem Biotechnol 28/29:865–875

    Google Scholar 

  • Ota H, Kurihara Y, Satoh S, Esashi Y (1991) Development of acetylene reduction (nitrogen-fixation) activity on and around imbibed plant seeds. Soil Biol Biochem 23:9–14

    Google Scholar 

  • Rivera-Ortiz JM, Burris RH (1975) Interaction among substrates and inhibitors of nitrogenase. J Bacteriol 123:537–545

    Google Scholar 

  • Silva-Avalos J, Richmond MG, Nagappan O, Kunz DA (1990) Degradation of the metal-cyano complex tetracyanonickelate(II) by cyanide-utilizing bacterial isolates. Appl Environ Microbiol 56:3664–3670

    Google Scholar 

  • Spackman DH, Stein WH, Moore S (1958) Automatic recording apparatus for use in the chromatography of amino acid. Anal Chem 30:1190–1206

    Google Scholar 

  • Taylor J (1962) The estimation of numbers of bacteria by tenfold dilution series. J Appl Bact 25:54–61

    Google Scholar 

  • Wilson PW, Knight SG (1952) Experiments in bacterial physiology, 3rd. edn. Burgess, Minneapolis, Minn

    Google Scholar 

  • Yemm EW, Cocking EC (1955) The determination of amino acids with ninhydrin. Analyst 80:209–213

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to H. Ota.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ota, H., Easashi, Y. Use of NaCN to increase the growth of N2-fixing bacteria in a model spermosphere mimicked by sucrose and amino acids leached by seeds. Biol Fertil Soils 22, 305–309 (1996). https://doi.org/10.1007/BF00334574

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00334574

Key words

Navigation