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A Feicht

Publications and source records attributed to A Feicht.

2 recordsLinked to original sources

Ovine ill-thrift in Nova Scotia. 9. Production of experimental quantities of isocyanide metabolites of Trichoderma hamatum.

Laboratory cultures of Trichoderma hamatum produce metabolites that are characterized by an isocyanide functionality. Three such metabolites predominate. One is the known compound trichoviridin (I). The other two, described here for the first time, are 3-(3-isocyano-6-oxabicyclo[3,1,0]hex-2-en-5-yl)acrylic acid (II) and a very unstable compound 3-(3-isocyanocyclopent-2-enylidene-)propionic acid (III). Production of these three metabolites by a random sample of wild isolates of the fungus has been examined. At least one of these isocyanides was isolated from all cultures in which the culture broth inhibited the growth of Micrococcus luteus. The relative amounts of the three isocyanides produced by individual isolates were not the same and cultures were found in which I, II, or III was the main product. The isocyanide III was produced by all wild isolates which had antibiotic activity in their culture broth, and it was present in the concentration range 2-40 mg X L-1.

Antibodies, Fungal↗

Nitrosamine formation from ternary nitrogen compounds.

When amides of pyrrolidine are heated with sodium nitrite, small amounts of NPYR are formed. Both the rate of reaction and the nitrosamine yield are increased when ethylene glycol and glycerine are used as solvents. Kinetic evidence suggests that these polyols react with the amide to form esters and the corresponding amine. The esters then react with sodium nitrite to give nitrite esters which rapidly nitrosate the amine. The heating of LDEA with sodium nitrite gives relatively high yields of NDELA in relatively short times and this nitrosation can be explained by this mechanistic hypothesis. 2-N,N-dimethylaminomethylpyrrole reacts very rapidly with nitrous acid at 25 degrees to give NDMA as the sole nitrosamine. This suggests a new mechanism of tertiary amine nitrosation.

Amides↗