Abstract:
Cysteine-rich peptides are a promising resource for a wide range of pharmacological applications
such as development of drug leads and as scaffolds for potential oral drug delivery due to their stable
disulfide framework. A handful of these compounds have been isolated from marine sponges and it
is speculated that plenty of them remain unexplored. In the present study, four peptides A, B, C and
D containing three disulfides were isolated from the aqueous extract of the deep-sea marine sponge
Stryphnus fortis (Demospongiae, Tetractinellida, Ancorinidae) from Norway, and were further
purified using RP-HPLC (Reverse Phase High Performance Liquid Chromatography). The mass
spectroscopic analysis using MALDI-TOF (Matrix-Assisted Laser Desorption/Ionization- Time Of
Flight) revealed monoisotopic masses of 3331.809 Da [M+H]+, 3349.731 Da [M+H]+, 3517.973 Da
[M+H]+, 3917.61 Da [M+H]+respectively for the four peptides A, B, C and D. The antimicrobial
activity was screened using a peptide adapted Micro dilution assay against E. coli (ATCC 25922), S.
aureus (ATCC 29213) and C. albicans (ATCC 90028) up to a concentration of 50 μM. The average
concentration derived from triplicates that exhibited a growth inhibition on visual inspection was
considered as the Minimum Inhibitory Concentration (MIC). Moderate antimicrobial activity for
peptide C was observed against S. aureus (MIC = 36.14 μM) and C. albicans (MIC = 18.07 μM).
However, no inhibition was observed against E. coli up to the highest concentration tested. The
human antimicrobial peptide LL 37 was used as the control (MIC value around 1-2 μM). The
sequence analysis of the four peptides, their structural characterization and investigation of their
potential applications are currently underway.
