ILGOVÁ, Jana, Milan GELNAR and Martin KAŠNÝ. Expression of a cysteine peptidase inhibitor from Eudiplozoon nipponicum (Monogenea). In 22nd Helminthological Days. 2015. ISBN 978-80-7444-032-8.
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Basic information
Original name Expression of a cysteine peptidase inhibitor from Eudiplozoon nipponicum (Monogenea).
Authors ILGOVÁ, Jana (703 Slovakia, guarantor, belonging to the institution), Milan GELNAR (203 Czech Republic, belonging to the institution) and Martin KAŠNÝ (203 Czech Republic, belonging to the institution).
Edition 22nd Helminthological Days, 2015.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 10600 1.6 Biological sciences
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/15:00080924
Organization unit Faculty of Science
ISBN 978-80-7444-032-8
Keywords in English cystatin; recombinant protein expression; Eudiplozoon nipponicum
Changed by Changed by: Mgr. et Mgr. Jana Ilgová, Ph.D., učo 223075. Changed: 24/7/2015 10:11.
Abstract
Our research is focused primarily on expression and characterization of cystatin produced by platyhelminth Eudiplozoon nipponicum. This blood-feeding ectoparasite of Cyprinus carpio (common carp) is a representative of the family Diplozooidae (Monogenea). Cystatins – cysteine peptidase inhibitors are produced by a wide range of organisms and belong to bioactive molecules with immunomodulatory and inhibitory properties. The transcriptomic data of E. nipponicum were analyzed for the presence of cystatin sequences. The partial nucleotide sequence was identified and the whole gene sequence was obtained by PCR, 3’/5’ RACE PCR and sequencing using cDNA as a template. Gene coding 98 amino acid cystatin of E. nipponicum with predicted molecular weight 10.85 kDa and theoretical pI 6.27 was inserted into pET19b expression vector and the obtained construct was transferred into E. coli competent cells (BL 21 strain). Expression of recombinant cystatin molecule was induced by adding IPTG to the cultivation media. The success of production was confirmed by mass spectrometry in a dominant protein band after the fractionation of the E. coli derived protein mixture by SDS-PAGE. Recombinant protein was produced in the insoluble form incorporated into inclusion bodies. The cystatin from E. nipponicum will be subsequently solubilized and tested for its functional and structural properties.
Links
GAP506/12/1258, research and development projectName: Interakce hostitel-parazit u krevsajících diplozoidních monogeneí: Výzkum vysoce specializovaných adaptací k parazitismu
Investor: Czech Science Foundation
GBP505/12/G112, research and development projectName: ECIP - Evropské centrum ichtyoparazitologie
Investor: Czech Science Foundation
MUNI/A/1484/2014, interní kód MUName: Analýzy diverzity biologických systémů různých úrovní a na různých škálách terestrického a akvatického prostředí (Acronym: BIDA4)
Investor: Masaryk University, Category A
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