Composition and Properties of Hydrogen Peroxide Decomposing Systems in Extracellular and Total Extracts from Needles of Norway Spruce (Picea abies L., Karst.) 1
Hydrogen peroxide (H 2 O 2 ) scavenging systems of spruce ( Picea abies ) needles were investigated in both extracts obtained from the extracellular space and extracts of total needles. As assessed by the lack of activity of symplastic marker enzymes, the extracellular washing fluid was free from in...
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Published in: | Plant physiology (Bethesda) Vol. 94; no. 1; pp. 312 - 319 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-09-1990
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Subjects: | |
Online Access: | Get full text |
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Summary: | Hydrogen peroxide (H
2
O
2
) scavenging systems of spruce (
Picea abies
) needles were investigated in both extracts obtained from the extracellular space and extracts of total needles. As assessed by the lack of activity of symplastic marker enzymes, the extracellular washing fluid was free from intracellular contaminations. In the extracellular washing fluid ascorbate, glutathione, cysteine, and high specific activities of guaiacol peroxidases were observed. Guaiacol peroxidases in the extracellular washing fluid and needle homogenates had the same catalytic properties,
i.e.
temperature optimum at 50°C, pH optimum in the range of pH 5 to 6 and low affinity for guaiacol (apparent
K
m
= 40 millimolar) and H
2
O
2
(apparent
K
m
= 1-3 millimolar). Needle homogenates contained ascorbate peroxidase, dehydroascorbate reductase, monodehydroascorbate reductase, glutathione reductase, and catalase, but not glutathione peroxidase activity. None of these activities was detected in the extracellular washing fluid. Ascorbate and glutathione related enzymes were freeze sensitive; ascorbate peroxidase was labile in the absence of ascorbate. The significance of extracellular antioxidants for the detoxification of injurious oxygen species is discussed. |
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Bibliography: | Present address: TU München, Institut für Botanik und Mikrobiologie, Arcisstr. 21, D-8000 München 2, Federal Republic of Germany. Present address: Department of Biochemistry, University College of Science, 35 Ballygunge Circular Rd., Calcutta 700109, India. This study was financially supported by a grant of the Bayerisches Staatsministerium für Landesentwicklung und Umweltfragen. |
ISSN: | 0032-0889 1532-2548 |