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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Planta 207 (1998), S. 207-216 
    ISSN: 1432-2048
    Keywords: Key words: Hydrogen peroxide generation ; Lignification ; NADPH oxidase ; Peroxidase ; Xylem ; Zinnia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The nature of the enzymatic system responsible for the generation of H2O2 in the lignifying xylem of Zinnia elegans (L.) was studied using the starch/KI method for monitoring H2O2 production and the nitroblue tetrazolium method for monitoring superoxide production. The results showed that lignifying xylem tissues are able to accumulate H2O2 and to sustain H2O2 production. Hydrogen peroxide production in the xylem of Z. elegans was sensitive to pyridine, imidazole, quinacrine and diphenylene iodonium, which are inhibitors of phagocytic plasma-membrane NADPH oxidase. The sensitivity of H2O2 production to the inhibitor of phospholipase C, neomycin, and to the inhibitor of protein kinase, staurosporine, and its reversion by the inhibitor of protein phosphatases, cantharidin, pointed to the analogies existing between the mechanism of H2O2 production in lignifying xylem and the oxidative burst observed during the hypersensitive plant cell response. A further support for the participation of an NADPH-oxidase-like activity in H2O2 production in lignifying xylem was obtained from the observation that areas of H2O2 production were superimposed on areas producing superoxide anion, the suspected product of NADPH oxidase, although attempts to demonstrate the existence of superoxide dismutase activity in intercellular washing fluid from Z. elegans were unsuccessful. Even so, the levels of NADPH-oxidase-like activity in microsomal fractions, and of peroxidase in intercellular washing fluids, are consistent with a role for NADPH oxidase in the delivery of H2O2 which may be further used by xylem peroxidases for the synthesis of lignins. This hypothesis was further confirmed through a direct histochemical probe based on the H2O2-dependent oxidation of tetramethylbenzidine by xylem cell wall peroxidases. These results are the first evidence for the existence of an NADPH oxidase responsible for supplying H2O2 to peroxidase in the lignifying xylem of Z. elegans.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-203X
    Keywords: Acidic isoperoxidases ; Basic isoperoxidases ; Capsicum annuum ; Medium ; Sequential release
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The establishment of suspension cell cultures from trimmed cotyledons of pepper (Capsicum annuum L.) provides a new experimental system for studying the relationship between release of peroxidase (EC 1.11.1.7) into the free intercellular spaces and plant cell growth. In contrast with several other species, the total peroxidase activity in the medium increased continuously during the post-exponential growth phase of the pepper cell culture, and this was correlated with the growth inhibition of pepper cells cultivated in suspension. The increase in the peroxidase activity in the culture medium was the consequence of a differential release of isoperoxidases, prominently marked by a primary release of basic isoperoxidases, followed by a strong increase in the level of acidic isoperoxidases. Thus, pepper cells cultures constitute a new experimental system for studying the regulation of the sequential release of basic and acidic isoperoxidases, which occurs during the growth cessation of plant cells.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1615-6102
    Keywords: Laccase activities ; Lignification ; Lupinus albus ; Peroxidase activities ; Secondary thickening ; Xylem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The post-exponential growth phase of lupin (Lupinus albus cv. Multolupa) hypocotyls is characterized by a strong deposition of lignins in the primary and secondary walls of the xylem vessels. Coinciding with this phenomenon, there is a clearly peroxidatic activity in both the primary cell walls and the outer-most layers of the secondary thickening of the xylem vessels, as demonstrated by 3,3′-diaminobenzidine cytochemistry. This activity was completely inhibited by KCN and the removal of H2O2 and was not due to laccase since this enzyme shows an almost total inability to oxidize 3,3′-diaminobenzidine both in the presence and in the absence of H2O2. The absence of laccase-like activities in cell walls of vascular cells was supported by the fact that cell wall proteins from vascular cells were only capable of oxidizing 3,3′-diaminobenzidine and coniferyl alcohol in the presence of H2O2. These results support the idea of an exclusive role of peroxidase (and exclude any role for laccase) in lignin formation in the secondary thickening of xylem vessels inLupinus.
    Type of Medium: Electronic Resource
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