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1.
Fundam Clin Pharmacol ; 31(3): 292-300, 2017 Jun.
Article in English | MEDLINE | ID: mdl-27885727

ABSTRACT

The objective of this study was to evaluate the anticancer properties of l-asparaginase purified from fungal isolate Fusarium culmorum ASP-87 against human T-cell leukemia cell line (Jurkat). The growth inhibitory and proapoptotic effects of purified l-asparaginase on Jurkat cell lines were investigated by determining its influence on cell viability, colony formation, DNA fragmentation, and cell cycle progression. The results revealed that purified l-asparaginase showed significant decrease in cell survival with IC50 value of 90 µg/mL (9 IU/mL). The enzyme inhibited colony formation and showed characteristic laddering pattern on agarose gel thereby confirming the induction of apoptosis. Further, cell cycle analysis revealed that the enzyme induced apoptotic cell death by arresting the growth of cells at G2 -M phase. However, the enzyme did not elicit any toxic effects on human erythrocytes. l-asparaginase purified from F. culmorum ASP-87 showed significant and selective cytotoxic and apoptotic effects on human T-cell leukemic cells in dose-dependent manner. Results of the study give leads for the anticancer effects of fungal l-asparaginase and its potential usefulness in the chemotherapy of leukemia.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Asparaginase/pharmacology , Cell Proliferation/drug effects , Fusarium/chemistry , Leukemia/drug therapy , Cell Line, Tumor , Cell Survival/drug effects , DNA Fragmentation/drug effects , Erythrocytes/drug effects , G2 Phase Cell Cycle Checkpoints/drug effects , Humans , Jurkat Cells
2.
N Biotechnol ; 32(2): 272-81, 2015 Mar 25.
Article in English | MEDLINE | ID: mdl-25481097

ABSTRACT

Membrane electrode assembly (MEA), a common arrangement used in direct methanol fuel cells, has been employed in a fed-batch mode microbial fuel cell (MFC), using mixed microbial population. This modification has been done for analyzing the prospect of obtaining increased power productivity. In addition, the electrodes have also been configured for the purpose of better current collection. Use of MEA as a replacement of the conventionally used 'separate membrane and electrode' arrangement has evidently resulted in reducing one of the limiting factors for higher power production in MFC, that is, its internal resistance. Open circuit potentials of more than 1 volt have been obtained for two MFC setups: (a) one consisting of an MEA and (b) the other having electrodes situated 2 cm apart from each other, but having better current collectors than the first setup. Power densities of 2212.57 mW m(-2) and 1098.29 mW m(-2) have been obtained at corresponding current densities of 5028.57 mA m(-2) and 3542.86 mA m(-2), respectively. The potential and power obtained for the MFC consisting of an MEA is quite significant compared to the other systems employed in this study.


Subject(s)
Bioelectric Energy Sources , Membranes, Artificial , Bacteria/ultrastructure , Biological Oxygen Demand Analysis , Dielectric Spectroscopy , Electricity , Electrochemical Techniques , Electrodes , Time Factors
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