Alternaria alternä»a(Fr一 Kelssler Is a natural pathogen tocrofton weed(Eå©aorium adenophorum),while th main 脉tor resulted indiseases was phytotoxln produced by the fun圳.ExPenments wereconducted to study the capability and culture conditions of toxin production,andthe purification,pathogemc range and physlolo9caf mechanism of*theismtOXlll. Bycomparingmethods ofexclsed leaf比st,seedlingso欢lug,nçš„dlepuncturingand seedgemlnatlonä»™lblting,needlepunctçš¿ngwasdetermlnedasthe malnbloassæ—¶ methods forA.alternaMtoxin.Byusingneedle punctunng,the toxinï¼Woducing ca帅ility of six isolates 501,503,402,LS,YN and AWAWhadhen assessd,andthe results showedthatthetoxinï¼producing则oåŠlity of Isolate 501 wasæ± e highest. By anaiyung the 4 tested solid media (whea,corn,soybean and rice),whetï¼meå±±M io40ï¼… water was SS讪巾kbrkdå‡ºåœ 501 to prcdoducetoxin.Thoe was not slplficå’– di地心mc of toxin pencing cpeility ontbee h…d cå’–çš¿ media(PSK,SCSC andand tcafjui比 ofcrofton weed).horder to facilitate the pepa觎ion ofcuhå®e meå±±urn,bloassay ofascptlcmtrate and pdncation oftoxln,PSx was sebded as the mæ—¶or culturemedium for producing toxins.Exprlmental results showed that themaximum toxin production wasåŠ tamed at 25℃,pH 4.13 under static anddarkcondltlon,and the optimum on扣åe time was 5ï¼7 då®s. P8thogClllC tOXlll PfodllCCd by ISO18tC 50ï¼WSS fC18tlVCï¼y StsblC.PH,temperature,storagetlmedldnotbave sl队lficantlmpactonthebloactlvltles of toxin.Dxlns prduced by Isolate 50 somewhat hadhost·speclDc activity,Sonchus deraceå Commellna communls,ä¹™mmeljna bengalensis,Robtnia pseuåŠ acacia,AIæ ¼rnanthera 英文嫡羹75phlloxero,è¡€s,hå§ar,a ananassa were highly sensitive and could be usedasbloassay materlalsto isolate andevaluate the toxin. The phytotoxln to the weed from Isolate 501 was isolated and purlhedby usingabstract,column chromatography and TLC.The maximallyabsorbed Peak wavelenph of the toxin produced by Isolate 501,which waspathogenlc toE adenOPhorum,was 296urn,and the Rfwas 0.34. Thetoxln had hlghblologlcal activity.hxln atåœgï¼gcould causetypical leafspotdlsease.Aftertreatment for 12 hours,toxin at 5 u gig couldcause stem atrophy and leafwlltofZï¼monthï¼oldE.adenoPhorum seedling.Thetoxln Influencedonthe permeåŠlllty ofcell membrane oft.adenophorumï¼eaves In vato,caused serious leakage of K"and Na",andIncreased MDA content of leaf tissue.Meanwhile,blobelcal actlvltles ofprotective enzymes suchas C矾 POD and APXdecreased,resulting Indisease ofE.adenoPhorum leaves. The studyofphyslologlcal mechanism oftoxlnprovedthatpathogenlcltyofA.alternatatoleaves oft.adenOPhorum hadcloserelatlonshlpwlth toxins.The research results would provldethetheoretlcalbasis ofdevelopment ofa mycoherblclde for crofton weed usingthe fingusandorå¿lsmï¼sourceherblclde usingthetoxln....
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