Uranium uptake and translocation by the arbuscular mycorrhizal fungus, Glomus intraradices, under root-organ culture conditions (original) (raw)

Contribution of hyphae and roots to uranium uptake and translocation by arbuscular mycorrhizal carrot roots under root-organ culture conditions

New Phytologist, 2003

Here, the respective contributions of the arbuscular mycorrhizal (AM) fungus Glomus intraradices and carrot ( Daucus carota ) roots to the uptake and translocation of uranium (U) were quantified and compared. • The U absorption by the AM fungus and roots was observed by growing mycorrhizal and nonmycorrhizal roots in two-compartment Petri plates. The central compartment allowed growth of roots and extraradical fungal hyphae. The external compartment (EC), which was labelled with 0.1 µ M 233 U, allowed growth of: hyphae only (hyphal compartment, HC), both mycorrhizal roots and hyphae (root hyphal compartment, RHC), or nonmycorrhizal roots (root compartment, RC). • The U concentration was 5.5 and 9.6 times higher for hyphae than for the mycorrhizal and nonmycorrhizal roots, respectively, both developing in the EC's. Translocation of U was similar for the RHC and the HC systems, and was 8 times higher for these two systems than for the RC system. • These results indicate that the U flux rate was higher in fungal hyphae than in roots, while the intraradical hyphae may significantly contribute to the U immobilization by mycorrhizal roots.

2005 Arbuscular mycorrhizal fungi mediated uptake (2005) 338-3.pdf

In a first experiment of soil contaminated with 137 Cs, inoculation with a mixture of arbuscular mycorrhizae enhanced the uptake of 137 Cs by leek under greenhouse conditions, while no effect on the uptake by ryegrass was observed. The mycorrhizal infection frequency in leek was independent of whether the 137 Cs-contaminated soil was inoculated with mycorrhizal spores or not. The lack of mycorrhizae-mediated uptake of 137 Cs in ryegrass could be due to the high root density, which was about four times that of leek, or due to a less well functioning mycorrhizal symbiosis than of leek. In a second experiment, ryegrass was grown for a period of four cuts. Additions of fungi enhanced 137 Cs uptake of all harvests, improved dry weight production in the first cut, and also improved the mycorrhizal infection frequencies in the roots. No differences were obtained between the two fungal inoculums investigated with respect to biomass production or 137 Cs uptake, but root colonization differed. We conclude that, under certain circumstances, mycorrhizae affect plant uptake of 137 Cs. There may be a potential for selecting fungal strains that stimulate 137 Cs accumulation in crops. The use of ryegrass seems to be rather ineffective for remediation of 137 Cscontaminated soil. D 2004 Published by Elsevier B.V.

Use of mycorrhizal fungi for the phytostabilisation of radio-contaminated environment (European project MYRRH): Overview on the scientific achievements

Radioprotection, 2005

Because plants significantly affect radionuclides (RN) cycling and further dispersion into the biosphere, it is important to understand the biological factors influencing RN plant uptake, accumulation and redistribution. In this respect, mycorrhizal fungi are of particular interest. The effects of ecto-mycorrhizal (ECM) and arbuscular mycorrhizal (AM) fungi on the transport of uranium (U) or radiocaesium (Cs) were investigated both under pot and in vitro culture conditions. Results obtained in vitro demonstrated that AM hyphae can take up and translocate U and Cs towards roots, while this uptake and translocation were not perceptible using pot culture systems with soil. These contrasting results could be due to different experimental conditions, including the K level in the external solution and the bio-availability of Cs. The in vitro studies also indicated that root colonisation by AM fungi might limit U and Cs root transport. Under pot culture conditions, they appeared to significantly reduce root to shoot translocation of U. Under the same conditions, ECM transport of Cs was demonstrated, and appeared to be dependent on fungal species. A better estimation of the potential use of mycorrhizal fungi for the phytoremediation of RN-contaminated areas is now available and will be further discussed.

Role and influence of mycorrhizal fungi on radiocesium accumulation by plants

Journal of Environmental Radioactivity, 2008

This review summarizes current knowledge on the contribution of mycorrhizal fungi to radiocesium immobilization and plant accumulation. These root symbionts develop extended hyphae in soils and readily contribute to the soil-to-plant transfer of some nutrients. Available data show that ecto-mycorrhizal (ECM) fungi can accumulate high concentration of radiocesium in their extraradical phase while radiocesium uptake and accumulation by arbuscular mycorrhizal (AM) fungi is limited. Yet, both ECM and AM fungi can transport radiocesium to their host plants, but this transport is low. In addition, mycorrhizal fungi could thus either store radiocesium in their intraradical phase or limit its root-to-shoot translocation. The review discusses the impact of soil characteristics, and fungal and plant transporters on radiocesium uptake and accumulation in plants, as well as the potential role of mycorrhizal fungi in phytoremediation strategies.

Comparison of arbuscular mycorrhizal fungal effects on the heavy metal uptake of a host and a non-host plant species in contact with extraradical mycelial network

Chemosphere, 2017

The effects of inoculation with an arbuscular mycorrhizal (AM) fungus on Cd and Ni tolerance and uptake in Medicago sativa, an AM host, and Sesuvium portulacastrum, a nonhost plant, were investigated in a greenhouse experiment. The plants were cultivated in sterilized sand in a two-compartmented system, which prevented root competition but enabled colonization of the whole substrate by AM fungal extraradical mycelium. M. sativa was either left non-inoculated or inoculated with the AM fungus Rhizophagus irregularis, and both plants were either cultivated without heavy metal (HM) addition or supplied with cadmium (Cd) or nickel (Ni), each in two doses. Additional pots with singly cultivated plants were established to control for the effect of the co-cultivation. AM significantly enhanced the growth of M. sativa and substantially increased its uptake of both HMs. The roots of S. portulacastrum became colonized by AM fungal hyphae and vesicles. The presence of the AM fungus in the cultivation system tended to increase the HM uptake of S. portulacastrum, but the effect was less consistent and pronounced than that in M. sativa. We conclude that AM fungal mycelium radiating from M. sativa did not negatively affect the growth and HM uptake of S. portulacastrum. On the contrary, we hypothesize that it stimulated the absorption and translocation of Cd and Ni in the non-host species. Thus, our results suggest that AM fungal mycelium radiating from mycorrhizal plants does not decrease the HM uptake of nonhost plants, many of which are considered promising candidate plants for phytoremediation.

Hyphal transport by a vesicular-arbuscular mycorrhizal fungus of N applied to the soil as ammonium or nitrate

Biology and Fertility of Soils, 1993

Transport of N by hyphae of a vesicular-arbuscular mycorrhizal fungus was studied under controlled experimental conditions. The N source was applied to the soil as 15NH~-or ~sNO~-. Cucumis sativus was grown for 25 days, either alone or in symbiosis with Glomus intraradices, in containers with a hyphal compartment separated from the root compartment by a fine nylon mesh. Mineral N was then applied to the hyphal compartment as lSNH~ or 15NO~-at 5 cm distance from the root compartment. Soil samples were taken from the hyphal compartment at 1, 3 and 5 cm distance from the root compartment at 7 and 12 days after labelling, and the concentration of mineral N in the samples was measured from 2 M KC1 extracts. Mycorrhizal colonization did not affect plant dry weight. The recovery of ~SN in mycorrhizal plants was 38 or 40070, respectively, when ~SNH~-or lsNO~-was applied. The corresponding values for nonmycorrhizal plants were 7 and 16070. The higher ~SN recovery observed in mycorrhizal plants than in nonmycorrhizal plants suggests that hyphal transport of N from the applied ~SN sources towards the host plant had occurred. The concentration of mineral N in the soil of hyphal compartments was considerably less in mycorrhizal treatments than in controls, indicating that the hyphae were able to deplete the soil for mineral N.

Uptake and transport of organic and inorganic nitrogen by arbuscular mycorrhizal fungi

2000

New information on N uptake and transport of inorganic and organic N in arbuscular mycorrhizal fungi is reviewed here. Hyphae of the arbuscular mycorrhizal fungus Glomus mosseae (Nicol. and Gerd.) Gerd. and Trappe (BEG 107) were shown to transport N supplied as 15 N-Gly to wheat plants after a 48 h labelling period in semi-hydroponic (Perlite), non-sterile, compartmentalised pot cultures. Of the 15 N supplied to hyphae in pot cultures over 48 h, 0.2 and 6% was transported to plants supplied with insufficient N or sufficient N, respectively. The increased 15 N uptake at the higher N supply was related to the higher hyphal length density at the higher N supply. These findings were supported by results from in vitro and monoxenic studies. Excised hyphae from four Glomus isolates (BEG 84, 107, 108 and 110) acquired N from both inorganic ( 15 NH 4 15 NO 3 , 15 NO 3 − or 15 NH 4 + ) and organic ( 15 N-Gly and 15 N-Glu, except in BEG 84 where amino acid uptake was not tested) sources in vitro during short-term experiments. Confirming these studies under sterile conditions where no bacterial mineralisation of organic N occurred, monoxenic cultures of Glomus intraradices Schenk and Smith were shown to transport N from organic sources ( 15 N-Gly and 15 N-Glu) to Ri T-DNA transformed, AM-colonised carrot roots in a long-term experiment. The higher N uptake (also from organic N) by isolates from nutrient poor sites (BEG 108 and 110) compared to that from a conventional agricultural field implied that ecotypic differences occur. Although the arbuscular mycorrhizal isolates used contributed to the acquisition of N from both inorganic and organic sources by the host plants/roots used, this was not enough to increase the N nutritional status of the mycorrhizal compared to non-mycorrhizal hosts.