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Fusarium oxysporium

Kido T, K Hashizume, K Soda (1978a) Purification and properties of nitroalkane oxidase from Fusarium oxysporium. J Bacterial 133 53-58. [Pg.140]

Aryl-3-arylimino[l,2,4]triazolo[3,4-c][l,2,4]dithiazoles 138 have been compared with dithane M-45 for their fungi-toxicity against Helmintosporium oryzae and Fusarium oxysporium <1983ABC1017>. [Pg.344]

Microbial bioconversion studies of manzamine A and ent-8-hydroxymanzamine A have shown that they can be metabolized by several microbial species.76 Preparative-scale fermentation of manzamine A with Fusarium oxysporium f. gladioli ATCC 11137 resulted in the isolation of the known ircinal A (61) as a major metabolite. Preparative-scale fermentation of enf-8-hydroxymanzamine A with Nocardia sp. ATCC 11925 and Fusarium oxysporium ATCC 7601 resulted in the isolation of the new major metabolite 12,34-oxamanzamine F (62). The latter metabolite showed no cytotoxicity against different cell lines (>10 pg/ml). [Pg.251]

Fusarium oxysporium (fungus) Yeast strain MKY3 Thermomonospora sp. (actinomycete)... [Pg.318]

Antibacterial activities against S. aureus and E. coli were moderate compared to penicillin and the antifungal activities against Cutvularia lunata and Fusarium oxysporium were lower compared to griseofulvin. [Pg.168]

The biosynthesis of lycomarasmine (38) has been studied in Fusarium oxysporium f lycopersici. Aspartic acid is a good precursor for the C4 unit, and... [Pg.86]


See other pages where Fusarium oxysporium is mentioned: [Pg.509]    [Pg.1021]    [Pg.324]    [Pg.2347]    [Pg.1021]    [Pg.447]    [Pg.612]    [Pg.844]    [Pg.188]    [Pg.7166]    [Pg.148]    [Pg.161]    [Pg.28]    [Pg.111]    [Pg.541]    [Pg.81]   
See also in sourсe #XX -- [ Pg.28 ]

See also in sourсe #XX -- [ Pg.81 ]




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