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Biomedical subjects

K A Seifert

Publications and source records attributed to K A Seifert.

4 recordsLinked to original sources

Microcoding: the second step in DNA barcoding.

After the process of DNA barcoding has become well advanced in a group of organisms, as it has in the economically important fungi, the question then arises as to whether shorter and literally more barcode-like DNA segments should be utilized to facilitate rapid identification and, where applicable, detection. Through appropriate software analysis of typical full-length barcodes (generally over 500 base pairs long), uniquely distinctive oligonucleotide 'microcodes' of less than 25 bp can be found that allow rapid identification of circa 100-200 species on various array-like platforms. Microarrays can in principle fulfill the function of microcode-based species identification but, because of their high cost and low level of reusability, they tend to be less cost-effective. Two alternative platforms in current use in fungal identification are reusable nylon-based macroarrays and the Luminex system of specific, colour-coded DNA detection beads analysed by means of a flow cytometer. When the most efficient means of rapid barcode-based species identification is sought, a choice can be made either for one of these methodologies or for basic high-throughput sequencing, depending on the strategic outlook of the investigator and on current costs. Arrays and functionally similar platforms may have a particular advantage when a biologically complex material such as soil or a human respiratory secretion sample is analysed to give a census of relevant species present.

Biodiversity↗

Nephrotoxigenic Penicillium species occurring on farm-stored cereal grains in western Canada.

The incidence of nephrotoxigenic Penicillium species on farm-stored cereals in western Canada was determined by morphological and metabolite profile examination. Of the 142 isolates examined 102 were toxin producers with 61 P. aurantiogriseum and 27 P. freii. Other nephrotoxigenic species included P. tricolor (6 isolates), P. verrucosum Chemotype II (4 isolates) and P. viridicatum Westling (4 isolates). The nephrotoxigenic Penicillium species profile for western Canada appears to differ from that of Denmark where P. verrucosum, P. cyclopium, P. freii and, to a lesser extent, P. aurantiogriseum, P. polonicum, and P. viridicatum predominate.

Agriculture↗

Secondary metabolites of Penicillium bilaii strain PB-50.

A phosphate-solubilizing strain of Penicillium bilaii was tested for the production of gliotoxin and other toxic compounds. The strain was fermented under five different conditions to allow the expression of various metabolites, including gliotoxin. These included Czapek-yeast extract medium under both shaken and still conditions as well as Czapek-yeast extract/malt extract/peptone medium and sucrose/glycerol medium in shake flasks. In addition, culture filtrate from an industrial fermentation of the fungus was examined. No gliotoxin was produced in any of the media. No other expected P. bilaii metabolites were found. Three compounds were identified in all samples: dibutyl phthalate, 1-(4-hydroxy-phenyl)ethanone and 4-hydroxy-3,6-dimethyl-2H-pyran-2-one. The production of other metabolites was dependent on the culture conditions. Two hyalodendrin derivatives were found in some fermentations and two related compounds were tentatively identified. None of the compounds found have been reported as toxic. The identity of the culture was confirmed by comparison with the ex-type culture of P. bilaii.

Acetophenones↗

Lignin degradation by Phanerochaete chrysosporium in hyperbaric oxygen.

Phanerochaete chrysosporium degraded aspen wood lignin as well in 2 atm O2 (1 atm = 101.325 kPa) as in 1 atm O2, but 3 atm O2 inhibited the fungus, and O2 pressures above 4 atm killed it. Lignin degradation in 5 atm of air was similar to that in 1 atm of O2, indicating that O2 concentration, not pressure, was the inhibitory factor. The selectivity with which P. chrysosporium metabolised lignin in preference to other wood components did not increase at O2 pressures above 1 atm.

Atmospheric Pressure↗