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Localization and speciation of arsenic in Glomus intraradices by synchrotron radiation spectroscopic analysis
Institution:1. Colegio de Postgraduados, Edafología, km 36.5 Carr. Mexico-Texcoco, Montecillo, Estado de México 56230, Mexico;2. U.S. Environmental Protection Agency, National Risk Management Research Laboratory, Land Remediation and Pollution Control Division, Cincinnati, OH, United States;3. Departamento de Biotecnología Agrícola, Instituto Politécnico Nacional, Centro Interdisciplinario de Investigación para el Desarrollo Integral Regional-IPN Unidad Sinaloa, Mexico;1. NOAA National Centers for Coastal Ocean Science, 1305 East West Highway, Silver Spring, MD 20910, USA;2. Consolidated Safety Services, 10301 Democracy Lane, Suite 300, Fairfax, VA 22030, USA;1. School of Geographic and Oceanographic Sciences, Nanjing University, Nanjing 210046 (China);2. Ministry of Education Key Laboratory of Protection and Development Utilization of Tropical Crop Germplasm Resources, Hainan University, Haikou 570228 (China)
Abstract:The protective mechanisms employed by arbuscular mycorrhizal fungi (AMF) to reduce the toxic effects of arsenic on host plants remain partially unknown. The goal of this research was identifying the in situ localization and speciation of arsenic (As) in the AM fungus Rhizophagus intraradices formerly named Glomus intraradices] exposed to arsenate As(V)]. By using a two-compartment in vitro fungal cultures of R. intraradices-transformed carrot roots, microspectroscopic X-ray fluorescence (μ-XRF), and microspectroscopic X-ray absorption near edge structure (μ-XANES), we observed that As(V) is absorbed after 1 h in the hyphae of AMF. Three hours after exposure a decrease in the concentration of As was noticed and after 24 and 72 h no detectable As concentrations were perceived suggesting that As taken up was pumped out from the hyphae. No As was detected within the roots or hyphae in the root compartment zone three or 45 h after exposure. This suggests a dual protective mechanism to the plant by rapidly excluding As from the fungus and preventing As translocation to the plant root. μ-XANES data showed that gradual As(V) reduction occurred in the AM hyphae between 1 and 3 h after arsenic exposure and was completed after 6 h. Principal component analysis (PCA) and linear combination fitting (LCF) of μ-XANES data showed that the dominant species after reduction of As(V) by R. intraradices extra-radical hyphal was As(III) complexed with a reduced iron(II) carbonate compound. The second most abundant As species present was As(V)–iron hydroxides. The remaining As(III) compounds identified by the LCF analyses suggested these molecules were made of reduced As and S. These results increase our knowledge on the mechanism of As transport in AMF and validate our hypotheses that R. intraradices directly participates in arsenic detoxification. These fungal mechanisms may help AMF colonized plants to increase their tolerance to As at contaminated sites.
Keywords:Arbuscular mycorrhizal fungi  Arsenate  Arsenite  Reduction  X-ray absorption near edge spectroscopy
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