PRIMARY INFORMATION |
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ID | 1221 |
PMID | 12712421 |
Year | 2002 |
Sequence | I/V-CLe-I/V-K-orn-I/V-fHdN |
Name | Bacitracin |
Length | 12 |
N-Terminal Modification | Thiazoline ring |
C-Terminal Modification | Free |
Linear/ Cyclic | Cyclic |
Chirality | Mix |
Chemical Modification | Condensed aminoacids 1 and 2 forming thiazoline ring, orn=D-Ornithine, I/V= Ile or Val |
Origin of Peptide | Produced as a mixture of closely related congeners by nonribosomal pathway catalyzed by large clusters of peptide and ketide synthetases and peptide/ketide “hybrid” synthetases, respectively |
Nature of Peptide/Cargo | Bactericidal antibiotic often used topically. It is a cyclic peptide that contains positively and negatively charged lateral chains at neutral pH and is composed of a mixture of L and D amino acids. |
Mechanism | Not mentioned |
Cargo Sequence/Structure | None |
Name of cargo
| Not applicable |
Assay | Fluorescein-labeled bacitracin and confocal microscopy, HPLC |
Enhancer | 2.75 µL phloretin loaded PC-liposomes (30 mol % phloretin) |
Properties of enhancer | Reduces the magnitude of the dipole potential in biological membranes |
Concentration | After 12 h from liposome application, 75µL of bacitracin–FITC 100 µM phosphate buffer is applied |
Incubation time | 48 Hours |
Tissue permeability (value with units) | Bacitracin Cumulative Amount(µg/cm2)=82.1±4.4 |
Tissue Sample | Human epidermis from abdominal sites of Caucasian females |
Ex vivo/In vivo/In vitro | ex vivo |
SECONDARY INFORMATION |
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STRUCTURE | |
SMILES | N.A. |