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The effect of acid irrigation on enzyme activities of the single partners of ectomycorrhizas from a limed stand of Norway spruce (Picea abies [L.] Karst.)

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Abstract

The aim of our investigations was to elucidate the effects of acid precipitation on some enzymes of the primary metabolism of ectomycorrhizas. Mycorrhizas of the type of Piceirhiza nigra Gronbach and of Russula ochroleuca (Pers.) Fr. and Tuber puberulum Berk. and Br. were collected from a stand of Norway spruce (Picea abies [L.] Karst.) during the growing seasons of 1991 and 1992. The experimental plots had been limed (Ca: 22 kmol ha-1, Mg: 20 kmol ha-1) in 1984 and exposed to acid irrigation (pH 2.7–2.8, H2SO4: 2 kmol ha-1 a-1) from 1984 to 1990. Crude extracts of mycorrhizas were assayed for the activities of glucose-6-phosphate dehydrogenase (G6P-DH, EC 1.1.1.49), 6-phosphogluconate dehydrogenase (EC 1.1.1.44), NADP-dependent isocitrate dehydrogenase (EC 1.1.1.42) and NAD-dependent glutamate dehydrogenase (EC 1.4.1.2). The influence of the experimental treatments on these enzyme activities of the primary metabolism was generally low. For P. nigra, the activity of G6P-DH was decreased on the irrigated plot (photometric determinations). This seems to be a selective effect on the fungal partner, since quantitative enzyme electrophoresis revealed a decrease in the percentage of the fungal enzyme activity in relation to the total enzyme activity, whereas the content of the fungal compound ergosterol was not affected. A decrease in the fungal G6P-DH activity could also be detected in mycorrhizas of Tuber puberulum. There was also a seasonal variation in the proportion of fungal activity of G6P-DH in relation to the total G6P-DH activity. In the photometric assay (total activity) the effect was not discernible. This is indicative of a degree of regulation between the two partners, which could only be detected by quantitative enzyme electrophoresis. In addition, it could be deduced from the electrophoretograms, that in the case of G6P-DH and 6PG-DH the fungal enzyme activity was dominating in all mycorrhizas studied whereas in the case of ICA-DH the fungal band varied from being conspicuous to absent in different species of mycorrhizas. The banding pattern of G6P-DH was reproducibly different for all investigated species of mycorrhizas.

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References

  • Agerer R 1988 Colour Atlas of Ectomycorrhizae. Einhorn-Verlag, Munich.

    Google Scholar 

  • Bilger I, Guillot V, Martin F and Le Tacon F 1989 Assessment of the contributions of glycolysis and the pentose phosphate pathway to glucose respiration in ectomycorrhizas and non-mycorrhizal roots of spruce (Picea abies L. Karsten). Ann. Sci. For. (Paris) (Suppl.) 46, 724s–727s.

    Google Scholar 

  • Boudot J P, Becquer T, Merlet D and Rouiller J 1994 Aluminium toxicity in declining forests: a general overview with a seasonal assessment in a silver fir forest in the Vosges mountains (France). Ann. Sci. For. 51, 27–51.

    Google Scholar 

  • Chen R D and Gadal P 1990 Structure, functions and regulation of NAD and NADP dependent isocitrate dehydrogenases in higher plants and in other organisms. Plant Physiol. Biochem. 28, 411–427.

    Google Scholar 

  • Dell B, Botton B, Martin F and Le Tacon F 1989 Glutamate dehydrogenases in ectomycorrhizas of spruce (Picea excelsa L.) and beech (Fagus sylvatica L.). New Phytol. 111, 683–692.

    Google Scholar 

  • Dighton J and Skeffington R A 1987 Effects of artificial acid precipitation on the mycorrhizas of Scots pine seedlings. New Phytol. 107, 191–202.

    Google Scholar 

  • Gallagher S R, Carroll E J Jr and Leonard R T 1986 A sensitive diffusion plate assay for screening inhibitors of protease activity in plant cell fractions. Plant Physiol. 81, 869–874.

    Google Scholar 

  • Gronbach E 1988 Charakterisierung und Identifizierung von Ektomykorrhizen in einem Fichtenbestand mit Untersuchungen zur Merkmalsvariabilität in sauer beregneten Flächen. Bibl. Mycol. 125, 1–216.

    Google Scholar 

  • Guttenberger M 1989 Untersuchungen zur Biochemie der Pilz-Baumwurzel-Symbiose. Proteinanalytik im Mikromaßstab. PhD thesis, Universität Tübingen.

  • Guttenberger M 1995 The protein complement of ectomycorrhizas. In Mycorrhiza: Function, Molecular Biology and Biotechnology. Eds. B Hock and A Varma. Springer Verlag, Berlin. 59–77.

    Google Scholar 

  • Guttenberger M, Compart U, Spägele S and Hampp R 1994a Proteolytic activity in the ectomycorrhizal fungus Amanita muscaria and its mycorrhizas on Betula pendula. Plant Physiol. (Suppl.) 105, 869.

    Google Scholar 

  • Guttenberger M, Neuhoff V and Hampp R 1991 A dot-blot assay for quantitation of nanogram amounts of protein in the presence of carrier ampholytes and other possibly interfering substances. Anal. Biochem. 196, 99–103.

    PubMed  Google Scholar 

  • Guttenberger M, Schaeffer C and Hampp R 1994b Kinetic and electrophoretic characterization of NADP dependent dehydrogenases from root tissues of Norway spruce (Picea abies (L.) Karst) employing a rapid one-step extraction procedure. Trees 8, 191–197.

    Google Scholar 

  • Kahl G 1974 Metabolism in plant storage tissue slices. Bot. Rev. 40, 263–314.

    Google Scholar 

  • Keller G 1992 Isozymes in isolates of Suillus species from Pinus cembra L. New Phytol. 120, 351–358.

    Google Scholar 

  • Klein R M and Perkins T D 1988 Primary and secondary causes and consequences of contemporary forest decline. Bot. Rev. 54, 1–43.

    Google Scholar 

  • Kreutzer K 1995 Effects of forest liming on soil processes. Plant Soil 168–169, 447–470.

    Google Scholar 

  • Kreutzer K and Weiss T 1998 The Höglwald field experiments-aims, concept and basic data. Plant Soil 199, 1–10.

    Google Scholar 

  • Kreutzer K, Göttlein A and Pröbstle P 1991 Dynamik und chemische Auswirkungen der Auflösung von Dolomitkalk unter Fichte (Picea abies [L.] Karst.) In Ökosystemforschung Höglwald. Eds. K Kreutzer and A Göttlein. Forstwiss. For. 39, 186–204. Parey, Hamburg, Berlin.

    Google Scholar 

  • Lowry O H and Passonneau J V 1972 A Fexible System of enzymatic Analysis. Academic Press, New York.

    Google Scholar 

  • Maijala P, Fagerstedt K V and Raudaskoski M 1991 Detection of extracellular cellulolytic and proteolytic activity in ectomycorrhizal fungi and Heterobasidion annosum (Fr.) Bref. New Phytol. 117, 643–648.

    Google Scholar 

  • Meier S 1991 Quality versus quantity-Optimizing evaluation of ectomycorrhizae for plants under stress. Environ. Pollut. 73, 205–216.

    PubMed  Google Scholar 

  • Namysl C 1992 Etude du métabolisme des racines d'Epicéa (Picea abies L. Karsten) soumises à une mycorhization par Amanita muscaria. Effets de l'ozone et de la sécheresse sur la mycorhization de l'Epicéa. PhD thesis, Université de Nancy.

  • Namysl C, Chalot M, Dell B, Dizengremel P, Botton B and Le Tacon F 1989 Changes in pathways for carbon and nitrogen assimilation in spruce roots under mycorrhization. Ann. Sci. For. (Paris) 46, 721s–723s.

    Google Scholar 

  • Nylund J-E and Wallander H 1992 Ergosterol analysis as a means of quantifying mycorrhizal biomass. Meth. Microbiol. 24, 77–88.

    Google Scholar 

  • Plassard C, Scheromm P, Mousain D and Salsac L 1991 Assimilation of mineral nitrogen and ion balance in the two partners of ectomycorrhizal symbiosis: data and hypothesis. Experientia 47, 340–349.

    Google Scholar 

  • Ramstedt M and Söderhäll K 1983 Protease, phenoloxidase and pectinase activities in mycorrhizal fungi. Trans. Br. Mycol. Soc. 81, 157–161.

    Google Scholar 

  • Read D J 1991 Mycorrhizas in ecosystems. Experientia 47, 376–391.

    Google Scholar 

  • Schaeffer C, Wallenda T, Guttenberger M and Hampp R 1995 Acid invertase in mycorrhizal and non-mycorrhizal roots of Norway spruce (Picea abies (L.) Karst) seedlings. New Phytol. 129, 417–424.

    Google Scholar 

  • Sen R 1990 Isozymic identifcation of individual ectomycorrhizas synthesized between Scots pine (Pinus sylvestris L.) and isolates of two species of Suillus. New Phytol. 114, 617–626.

    Google Scholar 

  • Sokal R R and Rohlf F J 1981 Biometry. Freeman, New York. 859p.

    Google Scholar 

  • Srivastava H S and Singh R P 1987 Role and regulation of L-glutamate dehydrogenase activity in higher plants. Phytochemistry 26, 597–610.

    Article  Google Scholar 

  • Taylor A F S, Brand F and Agerer R The response of a Norway spruce mycorrhizal community to acid irrigation and liming. Plant Soil (submitted).

  • Thelen H 1994 Die Anwendung quantitativer Enz y melektrophorese zur Bestimmung der partnerspezifischen Aktivitäten ausgewählter Dehydrogenasen aus Mykorrhizen von Amanita muscaria (L. ex Fr.) Hooker und Picea abies (L.) Karst. PhD thesis, Universität Tübingen.

  • Vézina L P, Margolis H A, McAfee B J and Delaney S 1989 Changes in the activity of enzymes involved with primary nitrogen metabolism due to ectomycorrhizal symbiosis on jack pine seedlings. Physiol. Plant. 75, 55–62.

    Google Scholar 

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Guttenberger, M., Zick, H., Thelen, H. et al. The effect of acid irrigation on enzyme activities of the single partners of ectomycorrhizas from a limed stand of Norway spruce (Picea abies [L.] Karst.). Plant and Soil 199, 71–81 (1998). https://doi.org/10.1023/A:1017995225968

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