Unknown

Dataset Information

0

Analysis of the loading and hydroxylation steps in lankamycin biosynthesis in Streptomyces rochei.


ABSTRACT: The biosynthetic gene cluster of lankamycin (LM), a 14-member macrolide antibiotic, is encoded on the 210-kb linear plasmid pSLA2-L in Streptomyces rochei 7434AN4. LM contains a 3-hydroxy-2-butyl group at the C-13 position, which is different from an ethyl group in erythromycin. The following two possibilities could be considered for the origin of this starter moiety of LM biosynthesis: (i) an extra module exists in the biosynthetic gene cluster and loads an additional acetate molecule, or (ii) 3-hydroxy-2-butyrate or its equivalent is loaded and incorporated as a starter. The former possibility was eliminated by the complete sequencing of pSLA2-L, which showed no extra module. On the other hand, the latter was confirmed by incorporation of deuterium in [3-(2)H]dl-isoleucine into the C-14 position of LM. The timing of hydroxylation reactions at the C-15 and C-8 positions of LM was studied by constructing disruptants of two P450 hydroxylase genes, lkmF (orf26) and lkmK (orf37). The lkmF disruptant produced 8-deoxylankamycin, while the lkmK disruptant produced both 15-deoxylankamycin and 8,15-dideoxylankamycin. These results clearly showed that LkmF is a C-8 hydroxylase and LkmK is a C-15 hydroxylase in LM biosynthesis and in addition suggested the order of hydroxylation steps; namely, hydroxylation may occur at first at C-15 by LkmK and then at C-8 by LkmF.

SUBMITTER: Arakawa K 

PROVIDER: S-EPMC1479134 | biostudies-literature | 2006 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Analysis of the loading and hydroxylation steps in lankamycin biosynthesis in Streptomyces rochei.

Arakawa Kenji K   Kodama Kazuya K   Tatsuno Satoshi S   Ide Sayoko S   Kinashi Haruyasu H  

Antimicrobial agents and chemotherapy 20060601 6


The biosynthetic gene cluster of lankamycin (LM), a 14-member macrolide antibiotic, is encoded on the 210-kb linear plasmid pSLA2-L in Streptomyces rochei 7434AN4. LM contains a 3-hydroxy-2-butyl group at the C-13 position, which is different from an ethyl group in erythromycin. The following two possibilities could be considered for the origin of this starter moiety of LM biosynthesis: (i) an extra module exists in the biosynthetic gene cluster and loads an additional acetate molecule, or (ii)  ...[more]

Similar Datasets

| PRJNA997791 | ENA
| PRJNA188025 | ENA
| PRJNA1048154 | ENA
| PRJNA999010 | ENA
| PRJNA1102097 | ENA
| PRJNA956841 | ENA
| S-EPMC5409476 | biostudies-literature
| S-EPMC10057877 | biostudies-literature
| S-EPMC107393 | biostudies-literature
| S-EPMC176625 | biostudies-other