The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.
Evidence for a Specific Uptake System for Iron Phytosiderophores in Roots of Grasses
Open accessAbstract
Roots of grasses in response to iron deficiency markedly increase the release of chelating substances (;phytosiderophores') which are highly effective in solubilization of sparingly soluble inorganic Fe(III) compounds by formation of Fe(III)phytosiderophores. In barley (Hordeum vulgare L.), the rate of iron uptake from Fe(III)phytosiderophores is 100 to 1000 times faster than the rate from synthetic Fe chelates (e.g. Fe ethylenediaminetetraacetate) or microbial Fe siderophores (e.g. ferrichrome). Reduction of Fe(III) is not involved in the preferential iron uptake from Fe(III)phytosiderophores by barley. This is indicated by experiments with varied pH, addition of bicarbonate or of a strong chelator for Fe(II) (e.g. batho-phenanthrolinedisulfonate). The results indicate the existence of a specific uptake system for Fe(III)phytosiderophores in roots of barley and all other graminaceous species. In contrast to grasses, cucumber plants (Cucumis sativus L.) take up iron from Fe(III)phytosiderophores at rates similar to those from synthetic Fe chelates. Furthermore, under Fe deficiency in cucumber, increased rates of uptake of Fe(III)phytosiderophores are based on the same mechanism as for synthetic Fe chelates, namely enhanced Fe(III) reduction and chelate splitting. Two strategies are evident from the experiments for the acquisition of iron by plants under iron deficiency. Strategy I (in most nongraminaceous species) is characterized by an inducible plasma membrane-bound reductase and enhancement of H(+) release. Strategy II (in grasses) is characterized by enhanced release of phytosiderophores and by a highly specific uptake system for Fe(III)phytosiderophores. Strategy II seems to have several ecological advantages over Strategy I such as solubilization of sparingly soluble inorganic Fe(III) compounds in the rhizosphere, and less inhibition by high pH. The principal differences in the two strategies have to be taken into account in screening methods for resistance to ;lime chlorosis'.
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Citations
Cites
Obligatory Reduction of Ferric Chelates in Iron Uptake by Soybeans
Chaney, R. L., Brown, J. C., & Tiffin, L. O. (1972) · Plant Physiology · doi:10.1104/pp.50.2.208 · Cited by 688
Physiological aspect of mugineic acid, a possible phytosiderophore of graminaceous plants
Takagi, S., Nomoto, K., & Takemoto, T. (1984) · Journal of Plant Nutrition · doi:10.1080/01904168409363213 · Cited by 567
Takagi, S.-I. (1976) · Soil Science and Plant Nutrition · doi:10.1080/00380768.1976.10433004 · Cited by 560
IRON ABSORPTION AND TRANSPORT IN MICROORGANISMS
Neilands, J. B. (1981) · Annual Review of Nutrition · doi:10.1146/annurev.nu.01.070181.000331 · Cited by 474
Römheld, V., & Marschner, H. (1983) · Plant Physiology · doi:10.1104/pp.71.4.949 · Cited by 402
Self-citationFree Space Iron Pools in Roots: Generation and Mobilization
Bienfait, H. F., van den Briel, W., & Mesland-Mul, N. T. (1985) · Plant Physiology · doi:10.1104/pp.78.3.596 · Cited by 304
Siderophore mediated absorption of iron
Hider, R. C. (2007) · Structure and Bonding · doi:10.1007/bfb0111310 · Cited by 261
Characterization of ferric reducing activity in roots of Fe‐deficient Phaseolus vulgaris
Bienfait, H. F., Bino, R. J., Bliek, A., et al. (1983) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1983.tb00757.x · Cited by 215
Localization and Capacity of Proton Pumps in Roots of Intact Sunflower Plants
Römheld, V., Müller, C., & Marschner, H. (1984) · Plant Physiology · doi:10.1104/pp.76.3.603 · Cited by 208
Self-citationCytosolic NADPH Is the Electron Donor for Extracellular FeIII Reduction in Iron-Deficient Bean Roots
Sijmons, P. C., van den Briel, W., & Bienfait, H. F. (1984) · PLANT PHYSIOLOGY · doi:10.1104/pp.75.1.219 · Cited by 144
Cited by
THE ROLE OF ROOT EXUDATES IN RHIZOSPHERE INTERACTIONS WITH PLANTS AND OTHER ORGANISMS
Bais, H. P., Weir, T. L., Perry, L. G., Gilroy, S., & Vivanco, J. M. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105159 · Cited by 4,682
Antimicrobial properties of tannins
Scalbert, A. (1991) · Phytochemistry · doi:10.1016/0031-9422(91)83426-l · Cited by 2,321
Enhanced Accumulation of Pb in Indian Mustard by Soil-Applied Chelating Agents
Blaylock, M. J., Salt, D. E., Dushenkov, S., Zakharova, O., Gussman, C., Kapulnik, Y., Ensley, B. D., & Raskin, I. (1997) · Environmental Science & Technology · doi:10.1021/es960552a · Cited by 1,257
Dissecting iron deficiency‐induced proton extrusion in Arabidopsis roots
Santi, S., & Schmidt, W. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02908.x · Cited by 616
Higuchi, K., Suzuki, K., Nakanishi, H., Yamaguchi, H., Nishizawa, N.-K., & Mori, S. (1999) · Plant Physiology · doi:10.1104/pp.119.2.471 · Cited by 435
Metadata
- Authors
- Römheld, V., & Marschner, H.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 1986-01-01
- Volume
- 80
- Issue
- 1
- Pages
- 175-180
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2070831559
- Cited by
- 992
- References
- 19
- FWCI
- 30.15
- Type
- journal article
- Language
- en
- Open access
- bronze
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