4C</sup> 低溫 .40<sup>°</sup>C 高溫及脫水干燥環(huán)境中水稻干尖線蟲存活率均顯著低于M9緩沖液處理和dsGFP處理。本研究成功構(gòu)建了水稻干尖線蟲AbTPS1、AbTPS2基因的dsRNA細(xì)菌表達(dá)體系,獲得的dsRNA具有明顯的RNAi效應(yīng),為利用RNA農(nóng)藥防治水稻干尖線蟲提供了技術(shù)支撐。-龍?jiān)雌诳W(wǎng)" />

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水稻干尖線蟲海藻糖6-磷酸合成酶基因雙鏈RNA細(xì)菌表達(dá)體系構(gòu)建

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關(guān)鍵詞:水稻干尖線蟲;海藻糖-6磷酸合成酶基因;雙鏈RNA;RNA干擾中圖分類號(hào): S435.114+8 (204號(hào) 文獻(xiàn)標(biāo)識(shí)碼:A 文章編號(hào):1000-4440(2025)05-0867-08

Abstract: Exogenous double-stranded RNA (dsRNA)can affct the gene expression of plant nematodes through RNAinterference(RNAi)to achieve the purpose ofpest control. The use of bacterial expression system for dsRNA preparation has high production efficiency and low cost, whichis the preferred strategy forlarge-scale preparation of dsRNA.Inorder toexplore theroleofbacterial dsRNA expression based on RNAi technology in the control of Aph 1 elechoidesbesseyi,in thisstudy,the trehalose-6-phosphate synthase genes AbTPS1 and AbTPS2of Aphelechoidesbes

seyi wereusedastarget genes to designand constructbacterial expressiondouble-strandedRNA(dsAbTPS1 and dsAbTPS2)vectorsandtransform Escherichiacoli HTi15(DE3).Theinduction expresionconditionsand extractionmethodsof dsRNA wereoptimized,andthe silencing eficiencyof dsRNA expressedbybacteriaontarget genes wasdetermined byfluorescence quantitative PCR,and the control effct of dsRNAonAphelenchoides beseyi was evaluated.The results showed that when the concentration of isopropyl ?β D -thiogalactoside(IPTG)was O.5 mmol/L and the induction time was 6 h ,thedsRNA yieldofthe AbTPS -L4440 expression vector HT115 strain constructed in this study reached the maximum. TheyieldofdsRNA extractedfromtheexpresionstrainsusing Trizolmethodandformamide method was significantlyhigher thanthatobtainedusing ethanol-sodiumchloride method.After treating Aphelenchoidesbeseyi with dsAbTPS1 and dsAbTPS2,the expresion levels of target genes AbTPS1and AbTPS2 were down-regulated.The survival rate of Aphelenchoidesbesseyi underlow temperature of 4 C ,high temperature of 40 ΔC and dehydration and drying conditions was significantlylowerthan thatinM9buffertreatmentanddsGFP treatment.Inthisstudy,thebacterialdsRNAexpresionsystem targeting AbTPS1 and AbTPS2 of A . besseyi was successfully constructed,and the obtained dsRNA exhibited obvious RNAi effects,which provided technical support for the use of RNA-based pesticides to control A .besseyi.

Key Words:Aphelenchoides besseyi; trehalose-6-phosphate synthase genes;double stranded RNA;RNA interferen

RNA干擾(RNAinterference,RNAi)是一種進(jìn)化上保守的序列特異機(jī)制,能調(diào)控大部分真核生物基因表達(dá)。(剩余12695字)

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