Oxalate production by fungi: its role in pathogenicity and ecology in the soil environment

1996 ◽  
Vol 42 (9) ◽  
pp. 881-895 ◽  
Author(s):  
Martin V. Dutton ◽  
Christine S. Evans

Oxalate secretion by fungi provides many advantages for their growth and colonization of substrates. The role of oxalic acid in pathogenesis is through acidification of host tissues and sequestration of calcium from host cell walls. The formation of calcium oxalate crystals weakens the cell walls, thereby allowing polygalacturonase to effect degradation more rapidly in a synergistic response. There is good correlation between pathogenesis, virulence, and oxalic acid secretion. Solubility of soil nutrients is achieved by soil-living species, when cations freed by oxalate diffusing in clay layers increases the effective solubility of Al and Fe. Oxalate retained in hyphal mats of mycorrhizal species increases phosphate and sulphate availability. The formation of calcium oxalate crystals provides a reservoir of calcium in the ecosystem. The ability of oxalate to bind divalent cations permits detoxification of copper, particularly evident in wood preserved with copper salts. Oxalate plays a unique role in lignocellulose degradation by wood-rotting basidiomycetes, acting as a low molecular mass agent initiating decay. In addition, in white-rot fungi oxalate acts as a potential electron donor for lignin-peroxidase catalysed reduction and chelates manganese, allowing the dissolution of Mn3+from the manganese–enzyme complex and thus stimulating extracellular manganese peroxidase activity. The biosynthesis and degradation of oxalate are discussed.Key words: oxalic acid, calcium oxalate, pathogenicity, fungi.

1987 ◽  
Vol 65 (9) ◽  
pp. 1952-1956 ◽  
Author(s):  
J. A. Traquair

Oxalic acid and crystals of calcium oxalate were produced during growth of Leucostoma cincta and L. persoonii on potato dextrose agar and in peach bark tissues. The identification of calcium oxalate was based on solubility characteristics, the results of KMnO4 titration, positive staining with silver nitrate – dithiooxamide, and crystal morphology as observed with light and scanning electron microscopes. Oxalic acid was detected by gas chromatography. This is the first report of oxalic acid production by both Leucostoma species causing peach canker. Calcium oxalate crystals observed on or near hyphae in culture were similar to crystals in artificially inoculated peach bark tissues. Addition of oxalic acid solutions alone to inner bark tissues caused maceration and necrosis. These results indicate a role for oxalic acid in the early stages of pathogenesis by Leucostoma spp. Tetragonal (bipyramidal) and prismatic calcium oxalate crystals formed on bark wounds treated with oxalic acid solutions were similar to those observed in infected tissues and in culture media amended with oxalic acid.


PEDIATRICS ◽  
1952 ◽  
Vol 10 (6) ◽  
pp. 660-666
Author(s):  
L. YING CHOU ◽  
W. L. DONOHUE

A case is reported of renal failure in a boy subsequent to recurrent calcium oxalate urinary calculi. The post mortem disclosed widespread deposits in the tissues of calcium oxalate crystals. These were particularly prominent in the kidneys and bone marrow. It is suggested that this is the end result of an "inborn error of metabolism" in which there was an excessive formation of oxalic acid.


1999 ◽  
Vol 77 (1) ◽  
pp. 179-187 ◽  
Author(s):  
Jon H Connolly ◽  
Walter C Shortle ◽  
Jody Jellison

The white-rot wood decay fungus Resinicium bicolor (Abertini & Schwein.: Fr.) Parmasto was studied for its ability to solubilize and translocate ions from the naturally occurring mineral strontianite. Resinicium bicolor colonized a soil mixture culture medium containing strontianite sand, solubilized strontium ions from this mineral phase, translocated the ions vertically, and reprecipitated the strontium into strontium-containing calcium oxalate crystals. Storage of the Sr in crystals was highest in mycelial cords and was dynamic in character. These results suggest that non-mycorrhizal saprotrophic fungi should be evaluated for their potential participation in forest nutrient cycling via biologically weathering parent material and translocating the mobilized mineral nutrients vertically within soils.Key words: fungi, strontium, calcium oxalate, translocation, soil, minerals nutrient cycling.


2002 ◽  
Vol 34 (2) ◽  
pp. 155-167 ◽  
Author(s):  
Virginia Souza-Egipsy ◽  
Jacek Wierzchos ◽  
Jose Vicente García-Ramos ◽  
Carmen Ascaso

AbstractThe chemical and ultrastructural features of the interface formed by different biotypes of saxicolous lichen species with their rock substrata were investigated in the semiarid habitat of the SE Iberian Peninsula and the relationships between the bioweathering patterns observed and lichen colonization selectivity towards the different rock substrata evaluated. Xanthoria parietina was able to fix to the rock substratum by the adherence of single cell walls from the lower cortex. Neofuscelia pulla used rhizines and loose groups of hyphae for attachment of the thallus to the rock. Colonization by the foliose lichen species was confined to the rock surface, while Diploschistes diacapsis was also able grow below the surface showing two types of hyphal growth. Minerals in close contact with cell walls were biochemically and biophysically weathered, but hyphae showing calcium oxalate crystals did not appear to be directly involved in the patterns observed. The textural characteristics of the substratum seemed to be related to the type of microorganism colonization: sedimentary rocks were more deeply colonized by lichens and other chasmolithic microorganisms than volcanic material. Calcium oxalate crystals were found in the medulla of N. pulla but not at the lichen-substratum interface. Crustose lichens such as D. diacapsis showed calcium oxalate crystals in the upper cortex and over the outside of fungal medullary hyphae but not in direct contact with the rock surface. Calcium oxalate precipitation seems to be related to the different metabolic activities of the mycobiont within the lichen thallus and to different species. D. diacapsis inhibits the growth of other microorganisms in close proximity to the thallus, whereas foliose species were associated with several communities of microorganisms.


2007 ◽  
Vol 34 (4) ◽  
pp. 339 ◽  
Author(s):  
Todd A. Kostman ◽  
Nathan M. Tarlyn ◽  
Vincent R. Franceschi

Many plant species accumulate calcium oxalate crystals in specialised cells called crystal idioblasts. In one species of crystal-forming plants (Pistia stratiotes L.; forming raphide crystals), it has been shown that ascorbic acid is the primary precursor of oxalic acid. The question remains if this is true of other calcium oxalate crystal-forming plants. One way of answering the above question is by examining ascorbic acid as the oxalic acid precursor in diverse species with a variety of crystal types. In this study we tested ascorbic acid as the primary precursor of oxalic acid in four different species, each forming one of the four, thus far, unexamined crystal types: water hyacinth, styloid (and raphide); tomato, crystal sand; winged-bean, prismatic; water lily, astrosclereids with surface prismatic crystals. Pulse–chase feeding of 1-[14C]-ascorbic acid followed by resin embedding, microautoradiography and light microscopy were employed to examine incorporation of label into calcium oxalate crystals. For the species and crystal types studied, ascorbic acid is the primary precursor of oxalic acid and further, oxalic acid is added to crystals in patterns that correlate with the age and type of crystal involved.


Author(s):  
H. J. Arnott ◽  
M. A. Webb ◽  
L. E. Lopez

Many papers have been published on the structure of calcium oxalate crystals in plants, however, few deal with the early development of crystals. Large numbers of idioblastic calcium oxalate crystal cells are found in the leaves of Vitis mustangensis, V. labrusca and V. vulpina. A crystal idioblast, or raphide cell, will produce 150-300 needle-like calcium oxalate crystals within a central vacuole. Each raphide crystal is autonomous, having been produced in a separate membrane-defined crystal chamber; the idioblast''s crystal complement is collectively embedded in a water soluble glycoprotein matrix which fills the vacuole. The crystals are twins, each having a pointed and a bidentate end (Fig 1); when mature they are about 0.5-1.2 μn in diameter and 30-70 μm in length. Crystal bundles, i.e., crystals and their matrix, can be isolated from leaves using 100% ETOH. If the bundles are treated with H2O the matrix surrounding the crystals rapidly disperses.


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