Three bioactive cyclic dipeptides from the Bacillus sp N strain associated with entomopathogenic nematode

被引:14
作者
Nishanth, Sasidharan Kumar [1 ]
Nambisan, Bala [1 ]
Dileep, C. [2 ]
机构
[1] Cent Tuber Crops Res Inst, Div Crop Protect, Thiruvananthapuram 695017, Kerala, India
[2] SD Coll, Dept Bot, Alappuzha, Kerala, India
关键词
Cryptococcus neoformans; Cyclo(Cyclo(L-Leu-D-Arg); Cytotoxicity; Apoptosis Antioxidant; BIOLOGICAL-ACTIVITY; DIKETOPIPERAZINES; ANTIOXIDANT; APOPTOSIS; PEPTIDES; CANCER; CELLS;
D O I
10.1016/j.peptides.2013.11.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In continuation of our search for new bioactive secondary metabolites from Bacillus cereus associated with entomopathogenic nematode (EPN), three cyclic dipeptides (CDPs), cyclo(L-Leu-D-Arg) (1), cyclo( 2hydroxy-Pro-L-Leu) (2), and cyclo(L-Val-L-Pro) (3) were purified from the ethyl acetate extract of B. cereus. The chemical structure of the compounds was identified by 1D, 2D NMR and HR-ESI-MS. Cyclo(LLeu-D-Arg) recorded best antifungal activity and the highest activity was recorded against Cry ptococcus neoformans (1 vg/mL), which is better than the standard antifungal agent amphotericin B. MU (344,5dimethylthiazol-2-y1)-2,5-diphenyltetrazolium bromide) assay was used for finding cell proliferation inhibition and cyclo(L-Leu-D-Arg) recorded significant activity against breast cancer cell line (MDAMB231) (IC50 value: 25 p,M) and the three cyclic dipeptides recorded no toxicity against normal human cell (fore skin (FS) normal fibroblast) up to 50 p,M except cyclo(L-Val-L-Pro). Cyclo(L-Leu-D-Arg) induced significant morphological changes and DNA fragmentation associated with apoptosis in MDAM-B231 cells by acridine orange/ethidium bromide staining and flow cytometry analysis. Out of three cyclic dipeptides tested only cyclo(2-hydroxy-Pro-L-Leu) recorded significant antioxidant activity. The hydroxyl radical scavenging activity of cyclo(2-hydroxy-Pro-L-Leu) is greater than BHA, the standard antioxidant agent. Cyclo(L-Leu-D-Arg) was isolated for the first time from a natural source with a D-arginine residue. To the best of our knowledge, this is the first time that the bioactivity of the isolated cyclic dipeptides is reported against medically important fungi and cancer cells. This study is a significant contribution to the knowledge of cyclo(L-Leu-D-Arg) from B. cereus as potential sources of new drugs in the pharmacological industry, especially as potent antifungal and anticancer agent. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 69
页数:11
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