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Identification and bioactivity evaluation of two novel temporins from the skin secretion of the European edible frog, Pelophylax kl. esculentus

Author:
Chen, Xiaole, Wang, He, Yang, Mu, Wang, Lei, Zhou, Mei, Chen, Tianbao, Shaw, Chris
Source:
Biochemical and biophysical research communications 2016 v.476 pp. 566-573
ISSN:
0006-291X
Subject:
Escherichia coli, Gram-negative bacteria, Gram-positive bacteria, Pelophylax, Staphylococcus aureus, anti-infective agents, antimicrobial peptides, bioactive properties, cDNA libraries, clones, complementary DNA, drugs, frogs, hemolysis, hydrophobicity, molecular weight, reversed-phase high performance liquid chromatography, secretion, skin (animal)
Abstract:
The amphibian temporins, amongst the smallest antimicrobial peptides (AMPs), are α-helical, amphipathic, hydrophobic and cationic and are active mainly against Gram-positive bacteria but inactive or weakly active against Gram-negative bacteria. Here, we report two novel members of the temporin family, named temporin-1Ee (FLPVIAGVLSKLFamide) and temporin-1Re (FLPGLLAGLLamide), whose biosynthetic precursor structures were deduced from clones obtained from skin secretion-derived cDNA libraries of the European edible frog, Pelophylax kl. esculentus, by ‘shotgun’ cloning. Deduction of the molecular masses of each mature processed peptide from respective cloned cDNAs was used to locate respective molecules in reverse-phase HPLC fractions of secretion. Temporin-1Ee (MIC = 10 μM) and temporin-1Re (MIC = 60 μM) were both found to be active against Gram-positive Staphylococcus aureus, but retaining a weak haemolytic activity. To our knowledge, Single-site substitutions can dramatically change the spectrum of activity of a given temporin. Compared with temporine-1Ec, just one chemically-conservative substitution (Val8 instead of Leu8), temporin-1Ee bearing a net charge of +2 displays broad-spectrum activity with particularly high potency on the clinically relevant Gram-negative strains, Escherichia coli (MIC = 40 μM). These factors bode well for translating temporins to be potential drug candidates for the design of new and valuable anti-infective agents.
Agid:
5247530