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Antiproliferative anthracycline pink red-like pigments produced by new bacterial soil strains identified as Streptomyces coelicoflavus and bioactivity of other compounds

International Conference on Environmental Microbiology & Microbial Ecology & International Conference on Ecology, Ecosystems & Conservation Biology

M. Menggad, A Mouslim, H Ayoubi, N Habti, S Menggad, S Moujabbir and E. Affar

University Hassan II Casablanca, Morocco University of Montreal, Canada

ScientificTracks Abstracts: J Ecosys Ecograph

DOI: 10.4172/2157-7625-C3-038

Abstract
Among 29 soil isolated actinomycetes, five new strains MFB11, MFB20, MFB21, MFB23 and MFB24 showed an intracellular hydrophobic pink red-like pigment production. These pigments present similar physio-chemical characteristics with anthracycline antibiotics of prodigiosin family. Crud extract and prepared fractions were tested by MTT on mice cancer cell line as well on human cancer cell line. The results indicated an important antiproliferative effect of the different strain pigments on the two organism cell types. Human cells were more sensitive to the pigments and presented different antiproliferative effect profiles. FACs analysis of this antiproliferative effect on cancer human cells line showed a cell cycle phase arrests at G1 and S. Nevertheless, negative antibacterial assay, Thin-layer chromatography (TLC) and interaction with organic solvents analysis of these pigments revealed their difference from known anthracycline antibiotics. Morphological, biochemical and gene coding 16S RNA sequence analysis allowed identification of the producer strains as Streptomyces coelicoflavus; known to produce important aminoglycoside antibiotics and other bioactive compounds but not anthracycline red-like pigments. Otherwise, two other strains produced water soluble Gram positive antibiotics and chloroform soluble bioactive compounds with strong and dramatic apoptotic antiproliferative activity as indicated by MTT and their cell cycle phase arrests at G0/G1 and G2.
Biography

Mohammed Menggad is a Professor in Hassan-II University of Casablanca, Morocco. He has completed Graduate diploma from Mohammed-V University, Rabat, Morocco. Postgraduate diploma and PhD from Paris XI University, France. He has experiences at Max-Planck-Institut fur Zellbiologie, Rosenh of Ladenburg, Germany and at Queen's University, Department of Biomedical and Molecular Sciences, Kingston, Canada.

E-mail: mengm106@yahoo.fr

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http://sacs17.amberton.edu/

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