Abstract
An extract of the skin of Schlegel's green tree frog, Rhacophorus schlegelii (Anura: Rhacophoridae), contained a protein that inhibited the growth of the Gram-negative bacterium Escherichia coli but was inactive against the Gram-positive bacterium Staphylococcus aureus. The protein was purified to near homogeneity by reverse-phase HPLC and amino acid sequence analysis of the products of an endoproteinase Glu-C digest identified the protein as histone H2B. The complete primary structure of the 125 amino acid residue Rhacophorus histone H2B was determined by nucleotide sequence analysis of a cloned cDNA encoding the protein. Mass spectrometry demonstrated that the protein isolated from the skin was not post-translationally modified. Histone fragments with antimicrobial activity were not identified in the Rhacophorus skin extract nor were cationic, α-helical antimicrobial peptides of the kind isolated from the skins of several other frog families. The data provide further evidence that histones play a role in the defense against microorganisms.
| Original language | English |
|---|---|
| Pages (from-to) | 1082-1086 |
| Number of pages | 5 |
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 312 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published (in print/issue) - 26 Dec 2003 |
Funding
This work was supported by a grant from the National Science Foundation (EPS-9720643) and by an Interdisciplinary Grant (03/12-8-03-01) and a Faculty Support Grant (NP/03/01) from the United Arab Emirates University. The authors thank Eva Lovas, Creighton University Medical School, for mass spectrometry measurements.
| Funders | Funder number |
|---|---|
| National Science Foundation | 03/12-8-03-01, EPS-9720643, NP/03/01 |
| United Arab Emirates University |