4.6 Article

All-D-cecropin B:: Synthesis, conformation, lipopolysaccharide binding, and antibacterial activity

期刊

MOLECULAR AND CELLULAR BIOCHEMISTRY
卷 218, 期 1-2, 页码 105-111

出版社

KLUWER ACADEMIC PUBL
DOI: 10.1023/A:1007293816634

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all-D-cecropin; solid phase peptide synthesis; circular dichroism conformation; lipopolysaccharide binding; antibacterial activity

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Cecropin B (LCB) is a natural peptide with antibacterial and antifungal properties. The enantiomer of LCB, containing all-D amino acids (DCB), was synthesized to examine its antibacterial and binding properties. The conformation of DCB was compared to its enantiomer by circular dichroism. Both the L- and D-peptides showed an identical induction of alpha -helical secondary structure. However, binding studies between Lipopolysaccharide (LPS) and DCB or LCB were studied with a dimethylmethylene blue spectrophotometric assay, showing the two enantiomeric peptides differed in their interaction with LPS. Antibacterial activity of DCB was determined against three Gram-negative bacteria, Pantoea agglomerans (ATCC 27996), Escherichia coli (ATCC 8739), and Pseudomonas aeruginosa (ATCC 17648), giving comparable results to LCB.

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