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Streptomyces rochei

Lankacldin A Lankacldinol A Lankacidin C Streptomyces rochei, Aspergillus niger Aspergillys sojae Trametes sanguinea... [Pg.190]

Various 8-0-14-Odl acylated Lankaddin C derivatives 14-O-Acylated lankacldin C Streptomyces rochei... [Pg.190]

Zaborina O, M Latus, J Eberspacher, LA Golovleva, F Lingens (1995) Purification and characterization of 6-chlorohydroquinol 1,2-dioxygenase from Streptomyces rochei 303 comparison with an analogous enzyme from Azotobacter sp. strain GPl. J Bacterial Yll 229-234. [Pg.494]

Rapid inactivation of added lincomycin was found to result from the growth of Streptomyces rochei in a synthetic medium the antibiotic was converted into lincomycin 3-phosphate [23670-99-7] (5, R = CH3, R = P03H2, R" = SCH3), C18H35N209PS, readily cleaved back to the antibiotic upon treating with alkaline phosphatase (53). [Pg.88]

Lankaddin A Lankaddinol A Lankaddin C Streptomyces rochei, Aspergillus niger As rgiliys sojae Trametes sangufnea... [Pg.190]

In 2003, Theodorakis et al. described the asymmetric synthesis of a key fragment corresponding to borrelidin (267, Figure 7.7). This macrolide natural product was isolated from Streptomyces rochei in 1949 and exhibits a broad antiviral and antibacterial prolile. Structurally, it contains an atypical 18-membered ring distinguished by a 1,3,5,7-skipped methylene chain, cyclopentane carboxylic acid, and conjugate cyanodiene unit. [Pg.208]

Penicillium sp. P. purpurogenum var. rubisclerotium, P. rugulosum, P. trzebinskii Streptomyces sp. S. rochei... [Pg.70]

See other pages where Streptomyces rochei is mentioned: [Pg.935]    [Pg.190]    [Pg.66]    [Pg.91]    [Pg.484]    [Pg.935]    [Pg.190]    [Pg.190]    [Pg.492]    [Pg.345]    [Pg.359]    [Pg.880]    [Pg.935]    [Pg.190]    [Pg.66]    [Pg.91]    [Pg.484]    [Pg.935]    [Pg.190]    [Pg.190]    [Pg.492]    [Pg.345]    [Pg.359]    [Pg.880]    [Pg.172]   
See also in sourсe #XX -- [ Pg.70 ]

See also in sourсe #XX -- [ Pg.492 ]



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