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. Author manuscript; available in PMC: 2013 May 1.
Published in final edited form as: Int J Antimicrob Agents. 2012 Mar 23;39(5):402–406. doi: 10.1016/j.ijantimicag.2012.02.003

Table 1.

Antibacterial activity of 30 antimicrobial peptides against Staphylococcus aureus USA300 LAC and Escherichia coli K12

Name (source)a Peptide sequenceb,c MIC (μM)
S. aureus E. coli
Apidaecin IA (insect) GNNRPVYIPQPRPPHPRI >100 >100
Ascaphin-8 (frog) GFKDLLKGAAKALVKTVLF-NH2 3.1 12.5
Brevinin-2-related (frog) GIWDTIKSMGKVFAGKILQNL-NH2 25 25
Buforin II (toad) TRSSRAGLQFPVGRVHRLLRK >71 >71
Clavanin-B (tunicate) VFQFLGRIIHHVGNFVHGFSHVF >100 >100
DASamP1 (synthetic)d FFGKVLKLIRKIF-NH2 3.1 >100
DASamP2 (synthetic)e IKWKKLLRAAKRIL-NH2 6.2 3.1
Desertcolin 1 (frog) GLADFLNKAVGKVVDFVKS-NH2 >100 >100
Distinctin chain 1 C23R (synthetic)f NLVSGLIEARKYLEQLHRKLKNRKV >92 >92
Drosocin (insect)g GKPRPYSPRPTSHPRPIRV >100 >100
Hyposin-5 (frog) FRPALIVRTKGTRL >30 >30
Isracidin (cow) RPKHPIKHQGLPQEVLNENLLRF >100 >100
Latarcin 3a (spider) SWKSMAKKLKEYMEKLKQRA >100 >100
Lycotoxin I (spider) IWLTALKFLGKHAAKHLAKQQLSKL 3.1 25
Maculatin 1.3 (frog) GLLGLLGSVVSHVVPAIVGHF-NH2 6.2 >100
Mastoparan M (insect) INLKAIAALAKKLL >100 25
Melectin (insect) GFLSILKKVLPKVMAHMK-NH2 12.5–25 12.5–25
Metalnikowin I (insect) VDKPDYRPRPRPPNM >100 >100
Misgurin (fish) RQRVEELSKFSKKGAAARRRK >84 >84
Parasin I (fish) KGRGKQGGKVRAKAKTRSS >84 >84
PGLa (frog) GMASKAGAIAGKIAKVALKAL-NH2 25 25
Piscidin 1 (fish) FFHHIFRGIVHVGKTIHRLVTG 3.1 12.5
Plantaricin chain A (bacteria)h GAWKNFWSSLRKGFYDGEAGRAIRR >38.9 >38.9
Ponericin L2 (insect) LLKELWTKIKGAGKAVLGKIKGLL 85 >25
Pseudin-1 (frog) GLNTLKKVFQGLHEAIKLINNHVQ >100 100
Ranatuerin 9 (frog) FLFPLITSFLSKVL 50 >100
Spinigerin (insect) HVDKKVADKVLLLKQLRIMRLLTRL >81 >81
Styelin A (tunicate) GFGKAFHSVSNFAKKHKTA-NH2 >100 >100
Temporin-LTc-3r (synthetic)i SLSRFLRFLKIVYRRAF-NH2 12.5 25
Uperin 7.1KRF (synthetic)j GWFDVVKHIAKRF-NH2 50 12.5
a

Six peptides identified to be active against S. aureus and studied further are indicated in bold.

b

Peptide sequences were obtained from the Antimicrobial Peptide Database [7], and mutated residues are shown in bold.

c

C-terminal amidation is represented by NH2.

d

A peptide mutant of temporin-PTa with S4K, P10R and L13F mutations. In contrast to peptides from natural sources (e.g. frogs, fish), those labelled with ‘synthetic’ are man-designed based on natural templates.

e

A peptide mutant of polybia-MPI with the following mutations: D2K, D8R and Q12R.

f

The sequence of this peptide corresponds to chain A of distinctin with residue C23 changed to R.

g

Residue T11 is not O-glycosylated.

h

The sequence of this peptide corresponds to chain A of plantaricin JK.

i

A mutant of temporin-LTc with three mutations: S7R, P14R and P15R.

j

This peptide was obtained by changing the last three residues SAV of uperin 7.1 to KRF.

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