Pregled bibliografske jedinice broj: 275056
Separation of plant viral satellite dsRNA using HPLC
Separation of plant viral satellite dsRNA using HPLC // Abstracts of the 29th Annual Meeting of the German Society for Cell Biology ; u: European Journal of Cell Biology. Supplement 85 (2006) (S1) MS9-5 / Bloemendal, Hans ; Jahn, Reinhard ; Schliwa, Manfred ; Werner, Sabine (ur.).
Jena: Elsevier, 2006. str. 112-112 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Separation of plant viral satellite dsRNA using HPLC
Autori
Rusak, Gordana ; Likić, Saša ; Krajačić, Mladen
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Abstracts of the 29th Annual Meeting of the German Society for Cell Biology ; u: European Journal of Cell Biology. Supplement 85 (2006) (S1) MS9-5
/ Bloemendal, Hans ; Jahn, Reinhard ; Schliwa, Manfred ; Werner, Sabine - Jena : Elsevier, 2006, 112-112
Skup
Annual Meeting of the German Society for Cell Biology (29 ; 2006))
Mjesto i datum
Braunschweig, Njemačka, 29.03.2006. - 01.04.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
cucumber mosaic virus(CMV); CMV satRNA
Sažetak
Satellite RNAs are plant subviral agents which depend on their helper viruses for replication and spread. Those accompanied with cucumber mosaic virus are certainly most important in agricultural production inducing severe symptoms, particularly in tomato. Both virus and the satellite generate sufficient quantity of double stranded replictive RNAs (dsRNAs). These stable replicative forms can be isolated from small amount of infected tissue by CF-11 cellulose chromatography and recognized in standard electrophoretic profile. The approach is often used in preliminary identification of this extremely harmful pathogen combination. In our investigation this standard method was followed by high-performance liquid chromatography (HPLC) for further separation of the satellite dsRNA. Samples were run on Helix DVB Column (3x50 mm ; Varian) at linear gradient, 44-80% B in 12 minutes ; temperature 30°C, flow rate=0, 45 ml/min (A=0.1M TEAA (triethylammonium acetate), 0.1 mM EDTA, B=0.1M TEAA, 0.1mM EDTA, 25% ACN). Separation resulted in chromatogram showing strong peak from which the material was collected and the satellite dsRNA identified by electrophoresis and PCR. Once standardized, HPLC offer clear evidence of satellite presence, without precipitation and electrophoresis. At the same time it can be used as a preparative approach resulting in very pure satellite for further analyses.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
Napomena
DOI: 10.1016/j.ejcb.2006.02.011 ; Rad je kao poster prezentiran i na skupu "31st International Symposium on High Performance Liquid Phase Separations and Related Techniques - HPLC 2007", održanom od 17-21.06.2007., Ghent, Belgija, objavljen uz međunarodnu recenziju u "Book of Abstracts", str. 905-905.
POVEZANOST RADA
Projekti:
0119150
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Akademija likovnih umjetnosti, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE