Skip to main content
Log in

Occurrence of uncommon polyamines in cultured tissues of maize

  • Physiology
  • Published:
In Vitro Cellular & Developmental Biology - Plant Aims and scope Submit manuscript

Summary

The uncommon polyamines, norspermidine and norspermine, were detected in maizein vitro cultures of three different genotypes. The common polyamines, spermidine and spermine, along with the diamine, putrescine, were also observed. The total amounts of the uncommon polyamines, norspermidine and norspermine, were comparable to the total amounts of the common polyamines, spermidine and spermine, in the maize tissues. The titer for norspermidine was 6- to 15-fold greater than that of its common counterpart (spermidine) in the three genotypes. Norspermidine was the predominant polyamine among all triamines and tetramines detected in cell cultures of two of the three genotypes of maize examined and was predominant along with spermine in the third genotype. Enzyme assays performed with extracts from callus of one of the genotypes suggested a likely mechanism to account for the biosynthesis of the uncommon polyamines in cultured maize cells, through the actions of putrescine aminopropyltransferase, polyamine oxidase, and Schiff-base reductase/decarboxylase enzyme activities. This is the first report of the detection of uncommon polyamines in maize tissues, as well as the first report of these uncommon polyamines in a monocotyledonous plant.

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

  • Adiga, P. R.; Prasad, G. L. Biosynthesis and regulation of polyamines in higher plants. Plant Growth Regul. 3:205–226; 1985.

    Article  CAS  Google Scholar 

  • Armstrong, C. L.; Green, C. E. Establishment and maintenance of friable, embryogenic maize callus and the involvement of L-proline. Planta 164:207–214; 1985.

    Article  CAS  Google Scholar 

  • Armstrong, C. L.; Green, C. E.; Phillips, R. L. Development and availability of germplasm with high type II culture formation response. Maize Cooperative Newsletter; 1991:92–93.

  • Bagga, S.; Dharma, A.; Phillips, G. C., et al. Evidence for the occurrence of polyamine oxidase in the dicotyledonous plantMedicago sativa L. (alfalfa). Plant Cell Rep. 10:550–554; 1991a.

    Article  CAS  Google Scholar 

  • Bagga, S.; Phillips, G. C.; Kuehn, G. D. Unique enzyme activities for polyamine biosynthesis in drought-tolerant alfalfa. Third International Congress of Plant Molecular Biology; October 6–12, 1991; Tucson, AZ; Abstr. 1559; 1991b.

  • Bagga, S.; Rochford, J.; Klaene, Z., et al. Putrescine aminopropyltransferase is responsible for biosynthesis of spermidine, spermine, and multiple uncommon polyamines in osmotic stress-tolerant alfalfa. Plant Physiol. 114:445–454; 1997.

    PubMed  CAS  Google Scholar 

  • Boget, N.; Torné, J. M.; Willadino, L., et al. Variations in endogenous polyamine content of maize calli obtained from zygotic and androgenetic embryos. Plant Cell Tissue Organ Cult. 40:139–144; 1995.

    Article  CAS  Google Scholar 

  • Bueno, M.; Garrido, D.; Matilla, A. Gene expression induced by spermine in isolated embryonic axes of chick-pea seeds. Physiol. Plant. 87:381–388; 1993.

    Article  CAS  Google Scholar 

  • Chu, C. C.; Wang, C. C.; Sun, C. S., et al. Establishment of an efficient medium for anther culture of rice through comparative experiments on the nitrogen sources. Sci. Sin. 18:659–668; 1975.

    Google Scholar 

  • Erdei, L.; Szegletes, Z.; Barabas, K., et al. Responses in polyamine titer under osmotic and salt stress in sorghum and maize seedlings. J. Plant Physiol. 147:599–603; 1996.

    CAS  Google Scholar 

  • Flores, H. E. Changes in polyamine metabolism in response to abiotic stress. In: Slocum, R. D.; Flores, H. E., ed. Biochemistry and physiology of polyamines in plants. Boca Raton, FL: CRC Press; 1991:213–228.

    Google Scholar 

  • Flores, H. E.; Protacio, C. M.; Signs, M. W.. Primary and secondary metabolism of polyamines in plants. Recent Adv. Phytochem. 23:329–393; 1989.

    CAS  Google Scholar 

  • Galston, A. W.; Sawhney, R. K. Polyamines in plant physiology. Plant Physiol. 94:406–410; 1990.

    PubMed  CAS  Google Scholar 

  • Khan A. U.; Mei, Y. H.; Wilson, T. A proposed function for spermine and spermidine: protection of replicating DNA against damage by singlet oxygen. Proc. Natl. Acad. Sci. USA 89:11426–11427; 1992.

    Article  PubMed  CAS  Google Scholar 

  • Kuehn, G. D.; Bagga, S.; Rodriguez-Garay, B., et al. Biosynthesis of uncommon polyamines in higher plants and their relation to abiotic stress responses. In: Flores, H. E.; Arteca, R. N.; Shannon, J. C., ed. Polyamines and ethylene: biochemistry, physiology, and interaction. Rockville, MD: Amer. Soc. Plant Physiol.; 1990:190–202.

    Google Scholar 

  • Marton, L. J.; Morris, D. R. Molecular and cellular functions of the polyamines. In: McCann, P. P., et al., ed. Inhibition of polyamine metabolism: biological significance and basis for new therapies. New York: Academic Press; 1987:79–105.

    Google Scholar 

  • Murashige, T.; Skoog, F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15:473–497; 1962.

    Article  CAS  Google Scholar 

  • Phillips, G. C.; Kuehn, G. D.. Uncommon polyamines in plants and other organisms. In: Slocum, R. D.; Flores, H. E., ed. Biochemistry and physiology of polyamines in plants. Boca Raton, FL: CRC Press; 1991:121–136.

    Google Scholar 

  • Rodriguez-Garay, B.; Phillips, G. C.; Kuehn, G. D. Detection of norspermidine and norspermine inMedicago sativa L. (alfalfa). Plant Physiol. 89:525–529; 1989.

    Article  PubMed  CAS  Google Scholar 

  • Schuber, F. Influence of polyamines on membrane functions. Biochem. J. 260:1–10; 1989.

    PubMed  CAS  Google Scholar 

  • Songstad, D. D.; Armstrong, C. L.; Petersen, W. L. AgNO3 increases type II callus production from immature embryos of maize inbred B73 and its derivatives. Plant Cell Rep. 9:699–702; 1991.

    Article  CAS  Google Scholar 

  • Tomes, D. T.; Ross, M. C.; Songstad, D. D.. Direct DNA transfer into intact plant cells via microprojectile bombardment. In: Gamborg, O. L.; Phillips, G. C., ed. Plant cell, tissue and organ culture—fundamental methods. Berlin, Heidelberg; Springer-Verlag; 1995:197–213.

    Google Scholar 

  • Torrigiani, P.; Scoccianti, V.; Bagni, N.Polyamine oxidase activity and polyamine content in maize during seed germination. Physiol. Plant. 74:427–432; 1988.

    Article  CAS  Google Scholar 

  • Van den Broeck, D.; Van der Straeten, D.; Van Montagu, M., et al. A group of chromosomal proteins is specifically released by spermine and loses DNA-binding activity upon phosphorylation. Plant Physiol. 106:559–566; 1994.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Koc, E.C., Bagga, S., Songstad, D.D. et al. Occurrence of uncommon polyamines in cultured tissues of maize. In Vitro Cell.Dev.Biol.-Plant 34, 252–255 (1998). https://doi.org/10.1007/BF02822717

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02822717

Key words

Navigation