Abstract

Phosphate (P) fixation to the soil solid phase is considered to be important for P availability and is often attributed to the strong binding of orthophosphate anion species. However, the fixation and subsequent immobilization of inositolhexa and pentaphosphate isomers (phytate) in soil is often much stronger than that of the orthosphate anion species. The result is that phytate is a main organic P form in soil and the dominating form of identifiable organic P. The reasons for the accumulation are not fully clear. Two hypothesis can be found in the literature in the last 20 years, the low activity of phytase (phosphatases) in soil, which makes phytate P unavailable to the plant roots, and, on the other hand, the strong binding of phytate to the soil solid phase with its consequent stabilization and accumulation in soil. The hypothesis that low phytase activity is responsible for phytate accumulation led to the development of genetically modified plant genotypes with a higher expression of phytase activity at the root surface and research on the effect of a higher phytate activity on P acquisition. Obviously, this hypothesis has a basic assumption, that the phytate mobility in soil is not the limiting step for P acquisition of higher plants from soil phytate. This assumption is, however, not justified considering the results on the sorption, immobilization and fixation of phytate to the soil solid phase reported in the last two decades. Phytate is strongly bound, and the P sorption maximum and probably the sorption strength of phytate P to the soil solid phase is much higher, compared to that of orthophosphate P. Mobilization of phytate seems to be a promising step to make it available to the plant roots. The excretion of organic acid anions, citrate and to a lesser extend oxalate, seems to be an important way to make phytate P available to the plants. Phytase activity at the root surface seems not be the limiting step in P acquisition from phytate. Phytate is not only bound to inorganic surfaces in soil but can also be bound, similar to orthophosphate, to humic surfaces via Fe or Al bridges. Humic-metal-phytate complexes may be transported in the soil solution to the roots where hydrolysis and uptake of the liberated P may occur. Research on this topic is strongly required.

Highlights

  • Myoinositolhexakisphosphate is the quantitative most important inositol phosphate found in soil

  • This review aims to give an overview on the main processes and the gaps of knowledge on inositol hexakisphosphates (IHP)

  • Richardson et al [37] ignored that in sand IHP was as good as P source as orthophosphate for two lupin species and Richardson et al [37]

Read more

Summary

Introduction

Myoinositolhexakisphosphate (phytate) is the quantitative most important inositol phosphate found in soil. Lower phosphorylated inositol phosphates seem to be of minor quantitative importance in soil. In the following paper we will term the highly phosphorylated inositol molecules inositol hexakisphosphates (IHP), taking in mind that phytate is the dominating molecule within this group and inositol pentakisphosphate isomers may be present. Po is often the dominant fraction in soil, often consisting of high molecular mass organic matter P, mainly associated with humic substances in soil [19]. Phosphate is strongly bound to the soil solid phase and is taken up by the plant roots as H2PO4− or HPO42− ion (Pi), the soil solution being replenished from the soil solid phase. The mechanisms by which IHP accumulate in soil and by which way phytate P can be acquired by the plant roots is not fully understood. This review aims to give an overview on the main processes and the gaps of knowledge on IHP accumulation in soil and IHP-P acquisition by the plants

The Binding of Inositol Hexakisphosphate in Soil
Mobilization of IHP from the Soil Solid Phase
The Role of Soil Microorganisms in the P Acquisition from IHP-P
Summary and Outlook
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.