Skip to main content
Log in

Cell wall peroxidase activity, hydrogen peroxide level and NaCl-inhibited root growth of rice seedlings

  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

The changes in cell-wall peroxidase (POD) activity and H2O2 level in roots of NaCl-stressed rice seedlings and their correlation with root growth were investigated. Increasing concentrations of NaCl from 50 to 150 mM progressively reduced root growth and increased ionically bound cell-wall POD activity. NaCl had no effect on covalently bound cell-wall POD activities. The reduction of root growth by NaCl is closely correlated with the increase in H2O2 level. Exogenous H2O2 was found to inhibit root growth of rice seedlings. Since ammonium and proline accumulation are associated with root growth inhibition caused by NaCl, we determined the effects of NH4Cl or proline on root growth, cell-wall POD activity and H2O2level in roots. External application of NH4Cl or proline markedly inhibited root growth, increased cell-wall POD activity and increased H2O2 level in roots of rice seedlings in the absence of NaCl. An increase in cell-wall POD activity and H2O2 level preceded inhibition of root growth caused by NaCl, NH4Cl or proline. NaCl or proline treatment also increased NADH-POD and diamine oxidase (DAO) activities in roots of rice seedlings, suggesting that NADH-POD and DAO contribute to the H2O2 generation in the cell wall of NaCl- or proline-treated roots. NH4Cl treatment increased NADH-POD activity but had no effect on DAO activity, suggesting that NADH-POD but not DAO is responsible for H2O2 generation in cell wall of NH4Cl-treated roots.

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

  • Allan A C and Fluhr R 1997 Two distinct sources of elicited reactive oxygen species in tobacco epidermal cells. Plant Cell 9, 1559–1572.

    Google Scholar 

  • Angelini R and Federico R 1989 Histochemical evidence of polyamine oxidation and hydrogen peroxide production in the cell wall. J. Plant Physiol. 135, 12–217.

    Google Scholar 

  • Angelini R, Manes F and Federico R 1990 Spatial and functional correlation between diamine-oxidase and peroxidase activities and their dependence upon de-etiolation and wounding in chickpea stems. Planta 182, 89–96.

    Google Scholar 

  • Bradley D J, Kjellbom P and Lamb C J 1992 Elicitor-and woundinduced oxidative cross-linking of a proline-rich plant cell wall protein: A novel, rapid defense response. Cell 70, 21–30.

    Google Scholar 

  • Carpita N C and Gilbeaut D M 1993 Structural models of primary cell walls in flowering plants: Consistency of molecular structure with the physical properties of the walls during growth. Plant J. 3, 1–30.

    Google Scholar 

  • Chen S L and Kao C H 1995 Cd induced changes in proline level and peroxidase activity in roots of rice seedlings. Plant Growth Regul. 17, 67–71.

    Google Scholar 

  • Cogoni A, Piras C, Farei R, Melis A and Floris G 1990 Hordeum vulgare seedlings amine oxidase. Purification and properties. Plant Physiol. 93, 818–821.

    Google Scholar 

  • Cosgrove D J 1997 Assembly and enlargement of the primary cell wall in plants. Annu. Rev. Cell Dev. Biol. 13, 171–201.

    Google Scholar 

  • Curtis C R 1971 Disc electrophoretic comparisons of proteins and peroxidases from Phaseolus vulgaris leaves infected with Agrobacterium tumefaciens. Can. J. Bot. 49, 333–337.

    Google Scholar 

  • Elstner E F and Heupel A 1976 Formation of hydrogen peroxide by isolated cell walls from horseradish (Armoracia lapathifolia Gilib). Planta 193, 283–289.

    Google Scholar 

  • Federico R and Angelini R 1986 Occurrence of diamine oxidase in the apoplast of pea epicotyls. Planta 167, 300–303.

    Google Scholar 

  • Frahry G and Schopfer P 1998 Hydrogen peroxidase production by roots and its stimulation by exogenous NADH. Physiol. Plant. 103, 395–404.

    Google Scholar 

  • Fry S C 1986 Cross-linking of matrix polymers in the growing cells of angiosperms. Annu. Rev. Plant Physiol. 37, 165–186.

    Google Scholar 

  • Gardiner M G and Cleland R 1974 Peroxidase changes during the cessation of elongation in Pisum sativnm stems. Phytochemistry 13, 1095–1098.

    Google Scholar 

  • Goldberg R, Liberman M, Mathieu C, Pierron M and Catesson A M 1987 Development of epidermal cell wall peroxidases along the mung been hypocotyl: possible involvement in the cell wall stiffening process. J. Exp. Bot. 38, 1378–1390.

    Google Scholar 

  • Gross G G 1977 Cell wall-bound malate dehydrogenase from horseradish. Phytochemistry 16, 319–321.

    Google Scholar 

  • Haynes R I and Goh K M 1978 Ammonium and nitrate nutrition of plants. Biol. Rev. 53, 465–510.

    Google Scholar 

  • Hohl M, Greiner H and Schopfer P 1995 The cryptic growth response of maize coleoptile and its relationship to H2O2-dependent cell wall stiffening. Physiol. Plant. 94, 491–498.

    Google Scholar 

  • Ishida A, Ookubo K and Ono K 1987 Formation of hydrogen peroxide by NAD(P)H oxidation with isolated cell wall-associated peroxidase from cultured liverwort cells, Marchantia polymorpha L. Plant Cell Physiol. 28, 723–726.

    Google Scholar 

  • Jana S and Choudhuri M A 1981 Glycolate metabolism of three submerged aquatic angiosperms during aging. Aquat. Bot. 12, 345–354.

    Google Scholar 

  • Lee T-M and Lin Y-H 1995 Changes in soluble and cell wall-bound peroxidase activities with growth in anoxia-treated rice (Oryza sativa L.) coleoptiles and roots. Plant Sci. 106, 1–7.

    Google Scholar 

  • Lin C C and Kao C H 1995 Levels of endogenous polyamines and NaCl-inhibited growth of rice seedlings. Plant Growth Regul. 17, 15–20.

    Google Scholar 

  • Lin C C and Kao C H 1996a Disturbed ammonium assimilation is associated with inhibition of roots in rice seedlings caused by NaCl. Plant Growth Regul. 18, 233–238.

    Google Scholar 

  • Lin C C and Kao C H 1996b Proline accumulation is associated with inhibiton of rice seedling root growth caused by NaCl. Plant Sci. 114, 121–128.

    Google Scholar 

  • Lin C C and Kao C H 1999 NaCl induced changes in ionically bound peroxidase activity in roots of rice seedlings. Plant Soil 216, 147–153.

    Google Scholar 

  • MacAdem J W, Sharp R E and Nelson C J 1992 Peroxidase activity in the leaf elongation zone of tall fescue. II. Spatial distribution of apoplastic peroxidase activity in genotypes differing in length of elongation zone. Plant Physiol. 99, 79–885.

    Google Scholar 

  • Mader M, Ongemach J and Schloss P 1980 The role of peroxidase isoenzyme groups of Nicotiana tabaccum in hydrogen peroxide formation. Planta 147, 467–471.

    Google Scholar 

  • Mader M, Nessel A and Schloss P 1986 Cell compartmentation and specific roles of isoenzymes. In Molecular and Physiological Aspects of Plant Peroxidases. Ed. H Greppin, C Penel and T Gaspar). pp 247–260. Univ. of Geneva Press, Geneva.

    Google Scholar 

  • Munns R 1993 Physiological responses limiting plant growth in saline soils: Some dogma and hypothesis. Plant Cell Environ. 16, 15–24.

    Google Scholar 

  • Naik B I, Goswami R G and Srivastawa S K 1981 A rapid and sensitive colorimetric assay of amine oxidase. Anal. Biochem. 111, 146–148.

    Google Scholar 

  • Neumann P M, Azaizeh H and Leon D 1994 Hardening of root cell walls: Growth inhibitory responses to salinity stress. Plant Cell Environ. 17, 303–309.

    Google Scholar 

  • Rengel Z 1992 The role of calcium in salt toxicity. Plant Cell Environ. 15, 625–632.

    Google Scholar 

  • Sanchez O J, Pan A, Nicolas G and Labrador E 1989 Relation of cell wall peroxidase activity with growth in epicotyls of Cicer arietinum. Effect of calmodulin inhibitors. Physiol. Plant. 75, 275–279.

    Google Scholar 

  • Schopfer P 1994 Histochemical demonstrations and localization of H2O2 in organs of higher plants by tissue printing on nitrocellulose paper. Plant Physiol. 104, 1269–1275.

    Google Scholar 

  • Schopher P 1996 Hydrogen peroxide-mediated cell-wall stiffening in vitro in maize coleoptiles. Planta 199, 43–49.

    Google Scholar 

  • Siegel S M 1953 On the biosynthesis of lignins. Physiol. Plant. 6, 134–139.

    Google Scholar 

  • Smith T A 1985 Di-and polyamine oxidases of higher plants. Biochem. Soc. Trans. 13, 319–322.

    Google Scholar 

  • Suzuki Y and Hagiwara M 1993 Purification and characterization of diamine oxidase from Zea mays shoot. Phytochemistry 33, 995–998.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ching Huei Kao.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lin, C.C., Kao, C.H. Cell wall peroxidase activity, hydrogen peroxide level and NaCl-inhibited root growth of rice seedlings. Plant and Soil 230, 135–143 (2001). https://doi.org/10.1023/A:1004876712476

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1004876712476

Navigation