
doi: 10.1038/204993a0 , 10.1038/204185a0
IN a previous communication1, from the analysis of a partial acid hydrolysate, the structure of polymyxin E1 was shown to be limited to two alternatives, the so-called 7 α and 8γ formulae. By applying the enzyme method of hydrolysis as devised by Suzuki et al. in their determinations of the structures of polymyxin B1 (ref. 2) and colistin A (ref. 3), the problem has now been resolved. We have isolated the peptides and from the hydrolysate of polymyxin E1 with the enzyme Nagarse (supplied by Teikoku Chemical Industry Co., Ltd., Osaka, Japan). The presence in particular of the second peptide eliminates the 8γ variant, and the structure of polymyxin E1 is therefore concluded to be (I; R=(+) 6-methyloctanoyl, X = D-Leu) and is therefore identical with that of colistin A (refs. 3 and 4).
Electrophoresis, Chemistry, Chemical Phenomena, Colistin, Research, Polymyxins, Peptides, Chemistry Techniques, Analytical, Anti-Bacterial Agents
Electrophoresis, Chemistry, Chemical Phenomena, Colistin, Research, Polymyxins, Peptides, Chemistry Techniques, Analytical, Anti-Bacterial Agents
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 33 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
