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Ciljno utišanje genov pri glivah z uporabo molekul dsRNA proizvedenih v bakterijskih celicah
ID Kveder, Ana (Author), ID Štajner, Nataša (Mentor) More about this mentor... This link opens in a new window

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Abstract
Glivni patogeni predstavljajo veliko nevarnost za zdravje ljudi in rastlin. Tradicionalno se jih zatira s fungocidi, ki pa imajo negativne učinke na okolje in zdravje. Ciljno utišanje genov z uporabo eksogeno proizvedene dvoverižne RNA (dsRNA) je obetavna alternativa, saj je njihovo delovanje zelo specifično. Glavna ovira za širšo uporabo je draga proizvodnja dsRNA. Rešitev je produkcija v bakterijah, največkrat uporabljena je Escherichia coli HT115(DE3), alternativa so tudi simbiotske bakterije rastlin, ki jih glive okužujejo. Za dostavo dsRNA molekul se lahko uporabijo žive bakterije, bakterijski lizati ali izolirane dsRNA molekule. Z uporabo živih bakterij lahko zagotovimo zaščito dsRNA pred fizičnimi in biološkimi dejavniki, vendar je treba pri tem zagotoviti varnost in preprečiti pobeg bakterij v okolje.

Language:Slovenian
Keywords:interferenca z RNA, glive, bakterijska proizvodnja dsRNA, Escherichia coli HT115(DE3), fitopatogeni
Work type:Bachelor thesis/paper
Typology:2.11 - Undergraduate Thesis
Organization:BF - Biotechnical Faculty
Publication status:Published
Publication version:Version of Record
Year:2025
PID:20.500.12556/RUL-170444 This link opens in a new window
COBISS.SI-ID:241562371 This link opens in a new window
Publication date in RUL:06.07.2025
Views:256
Downloads:41
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Secondary language

Language:English
Title:Targeted gene silencing in fungi using dsRNA molecules produced in bacterial cells
Abstract:
Fungal pathogens pose a major threat to both human and plant health. Traditionally, they are controlled using fungicides; however, these have adverse environmental and health effects. Targeted gene silencing through the use of exogenously produced double-stranded RNA (dsRNA) represents a promising alternative due to its high specificity. The primary obstacle to broader application is the high cost of dsRNA production. Bacterially produced dsRNA could offer a solution. Escherichia coli HT115(DE3) is most commonly used, although symbiotic, plant-associated bacteria inhabiting hosts susceptible to fungal infection are also being explored. For dsRNA delivery, live bacteria, bacterial lysates, or purified dsRNA molecules can be employed. The use of live bacteria offers protection of dsRNA against physical and biological degradation; however, strict biosafety measures are necessary to prevent environmental release of these bacteria.

Keywords:RNA interference, fungi, bacterial production of dsRNA, Escherichia coli HT115(DE3), phytopathogens

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