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Fig. 1 | BMC Biotechnology

Fig. 1

From: Unusual acylation of chloramphenicol in Lysobacter enzymogenes, a biocontrol agent with intrinsic resistance to multiple antibiotics

Fig. 1

Chemical structure of the antifungal natural product HSAF and the unusual chloramphenicol derivatives (compounds 1–3) produced in Lysobacter enzymogenes C3. 1, chloramphenicol-3'-isobutyrate; 2, chloramphenicol-1'-isobutyrate; 3, chloramphenicol-3'-isovalerate. The structure of chloramphenicol and the usual product of chloramphenicol acyltransferase, chloramphenicol-3'-acetate, is also shown

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