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  4. White lupin has developed a complex strategy to limit microbial degradation of secreted citrate required for phosphate acquisition

White lupin has developed a complex strategy to limit microbial degradation of secreted citrate required for phosphate acquisition

Author(s)
Weisskopf, Laure
Abou-Mansour, Eliane
Fromin, Nathalie
Tomasi, Nicola
Santelia, Diana
Edelkott, Iris
Neumann, Günter
Aragno, Michel  
Institut de biologie  
Tabacchi, Raffaele  
Institut de chimie  
Martinoia, Enrico
Date issued
2006
In
Plant, Cell & Environment, Wiley, 2006/29/5/917-927
Subjects
<i>Lupinus albus</i> chitinase glucanase isoflavonoids phenolics protection
Abstract
White lupins (<i>Lupinus albus</i> L.) respond to phosphate deficiency by producing special root structures called cluster roots. These cluster roots secrete large amounts of carboxylates into the rhizosphere, mostly citrate and malate, which act as phosphate solubilizers and enable the plant to grow in soils with sparingly available phosphate. The success and efficiency of such a P-acquisition strategy strongly depends on the persistence and stability of the carboxylates in the soil, a parameter that is influenced to a large extent by biodegradation through rhizosphere bacteria and fungi. In this study, we show that white lupin roots use several mechanisms to reduce microbial growth. The abundance of bacteria associated with cluster roots was decreased at the mature state of the cluster roots, where a burst of organic acid excretion and a drastic pH decrease is observed. Excretion of phenolic compounds, mainly isoflavonoids, induced fungal sporulation, indicating that vegetative growth, and thus potential citrate consumption, is reduced. In addition, the activity of two antifungal cell wall-degrading enzymes, chitinase and glucanase, were highest at the stage preceding the citrate excretion. Therefore, our results suggest that white lupin has developed a complex strategy to reduce microbial degradation of the phosphate-solubilizing agents.
Publication type
journal article
Identifiers
https://libra.unine.ch/handle/20.500.14713/61809
DOI
10.1111/j.1365-3040.2005.01473.x
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