Previous Page  34 / 37 Next Page
Information
Show Menu
Previous Page 34 / 37 Next Page
Page Background

Page 89

Notes:

conferenceseries

.com

Volume 9, Issue 9 (Suppl)

J Cancer Sci Ther, an open access journal

ISSN: 1948-5956

World Cancer 2017

October 19-21, 2017

25

th

WORLD CANCER CONFERENCE

October 19-21, 2017 | Rome, Italy

J Cancer Sci Ther 2017, 9:9(Suppl)

DOI: 10.4172/1948-5956-C1-112

Studies on anti-neoplastic enzyme: enhanced L-asparaginase activity by filamentous fungus from the

Brazilian Savanna using Plackett-Burman Design for screening of culture medium variables

Pérola Magalhães

1

, Marcela Medeiros de Freitas

1

, Paula Monteiro Souza

1

, Samuel Cardoso

1

, Edilvaldo Ximenes

1

and

Adalberto Pessoa

2

1

University of Brasília, Campus Darcy Ribeiro, Brazil

2

University of São Paulo, Brazil

L

-asparaginase is an enzyme used for treatment of Acute Lymphoblastic Leukemia (ALL) in children. Neoplastic cells

cannot synthesize L-asparagine unlike normal cells due the absence of L-asparagine synthetase; therefore they obtain the

required asparagine from circulating pools. It is important to find new sources of Lasparaginase producing microorganisms

that can avoid adverse effects obtained from bacterial L-asparaginase, such as anaphylactoid reactions. Screening and selection

of the fungi and optimum concentration of the medium component are very important to determine the overall economic

feasibility of the production process. Therefore, the purpose of this study was to evaluate the important variables that influence

Lasparaginase activity by a filamentous fungus isolated from the Brazilian Savanna soil. Eleven independent variables were

considered to evaluate their effect on Lasparaginase activity by a filamentous fungus (DCFS10) in submerged fermentation.

The different variables were prepared in two concentration levels, (-1) low level and (+1) high level. L-asparaginase activity

was assayed by measuring the amount of aspartate hydroxamate produced from asparagine and hydroxylamine according

to Drainas et al. (1977). The results obtained from PBD showed a wide range of Lasparaginase activity, from 0.5 U/g ± 0.018

to 6.5 U/g ± 0.284. Studies are being conducted in order to purify L-asparaginase produced in this culture medium. This

study showed that the screening of culture medium variables using Plackett-Burman increased L-asparaginase activity of a

filamentous fungus isolated from the Brazilian Savanna soil as a potential novel anti-leukemic source from eukaryote cell.

perolamagalhaes@unb.br