作物学报
作物學報
작물학보
ACTA AGRONOMICA SINICA
2015年
2期
308-317
,共10页
吴林坤%黄伟民%王娟英%吴红淼%陈军%秦贤金%张重义%林文雄
吳林坤%黃偉民%王娟英%吳紅淼%陳軍%秦賢金%張重義%林文雄
오림곤%황위민%왕연영%오홍묘%진군%진현금%장중의%림문웅
地黄%磷脂脂肪酸%末端限制性片段长度多态性%微生物多样性%植物根际
地黃%燐脂脂肪痠%末耑限製性片段長度多態性%微生物多樣性%植物根際
지황%린지지방산%말단한제성편단장도다태성%미생물다양성%식물근제
Rehmannia glutinosa%PLFA%T-RFLP%Microbial diversity%Plant rhizosphere
以野生地黄为试验材料,设置野生地黄头茬土壤、重茬土壤和原茬土壤处理,未种植任何作物为对照,于块根膨大中期采集土样,通过磷脂脂肪酸法(PLFA)和末端限制性片段长度多态性(T-RFLP)技术,分析不同连作年限野生地黄的根际微生物生物量和群落结构变化。PLFA 分析结果表明,不同处理情况下地黄根际土壤微生物群落结构存在明显差异,与头茬地黄根际土壤相比,重茬地黄土壤微生物总量显著下降,并且细菌/真菌比例下降。T-RFLP 分析结果表明,不同连作年限地黄根际土壤细菌群落结构存在一定差异,野生状态地黄土壤和头茬土壤菌群较为相似,变形菌门和厚壁菌门占据优势地位。野生状态地黄和头茬地黄根际富含 Bacillus、Pseudomonas 等有益生防菌,而重茬地黄根际土壤滋生大量病原菌如 Clostridium sp.、Flexibacter polymorphus 和 Clostridium ghoni,有益菌群和纤维素降解菌群减少, qRT-PCR 定量分析也显示,野生状态地黄和头茬地黄土壤中假单胞菌数量都显著高于重茬地黄土壤。总之,野生地黄存在连作障碍问题,导致野生地黄根际有益菌数量减少而病原菌大量滋生,从而降低了野生地黄抵御病害的能力,使重茬野生地黄生长发育差,产量大幅降低。
以野生地黃為試驗材料,設置野生地黃頭茬土壤、重茬土壤和原茬土壤處理,未種植任何作物為對照,于塊根膨大中期採集土樣,通過燐脂脂肪痠法(PLFA)和末耑限製性片段長度多態性(T-RFLP)技術,分析不同連作年限野生地黃的根際微生物生物量和群落結構變化。PLFA 分析結果錶明,不同處理情況下地黃根際土壤微生物群落結構存在明顯差異,與頭茬地黃根際土壤相比,重茬地黃土壤微生物總量顯著下降,併且細菌/真菌比例下降。T-RFLP 分析結果錶明,不同連作年限地黃根際土壤細菌群落結構存在一定差異,野生狀態地黃土壤和頭茬土壤菌群較為相似,變形菌門和厚壁菌門佔據優勢地位。野生狀態地黃和頭茬地黃根際富含 Bacillus、Pseudomonas 等有益生防菌,而重茬地黃根際土壤滋生大量病原菌如 Clostridium sp.、Flexibacter polymorphus 和 Clostridium ghoni,有益菌群和纖維素降解菌群減少, qRT-PCR 定量分析也顯示,野生狀態地黃和頭茬地黃土壤中假單胞菌數量都顯著高于重茬地黃土壤。總之,野生地黃存在連作障礙問題,導緻野生地黃根際有益菌數量減少而病原菌大量滋生,從而降低瞭野生地黃牴禦病害的能力,使重茬野生地黃生長髮育差,產量大幅降低。
이야생지황위시험재료,설치야생지황두치토양、중치토양화원치토양처리,미충식임하작물위대조,우괴근팽대중기채집토양,통과린지지방산법(PLFA)화말단한제성편단장도다태성(T-RFLP)기술,분석불동련작년한야생지황적근제미생물생물량화군락결구변화。PLFA 분석결과표명,불동처리정황하지황근제토양미생물군락결구존재명현차이,여두치지황근제토양상비,중치지황토양미생물총량현저하강,병차세균/진균비례하강。T-RFLP 분석결과표명,불동련작년한지황근제토양세균군락결구존재일정차이,야생상태지황토양화두치토양균군교위상사,변형균문화후벽균문점거우세지위。야생상태지황화두치지황근제부함 Bacillus、Pseudomonas 등유익생방균,이중치지황근제토양자생대량병원균여 Clostridium sp.、Flexibacter polymorphus 화 Clostridium ghoni,유익균군화섬유소강해균군감소, qRT-PCR 정량분석야현시,야생상태지황화두치지황토양중가단포균수량도현저고우중치지황토양。총지,야생지황존재련작장애문제,도치야생지황근제유익균수량감소이병원균대량자생,종이강저료야생지황저어병해적능력,사중치야생지황생장발육차,산량대폭강저。
The soils sampled from the four different plots, including the newly planted, the two-year monocultured, the wild R. glutinosa and the control without growing R. glutinosa, were used to study the changes in microbial biomass and community composition using phospholipid fatty acid (PLFA) and terminal restriction fragment length polymorphism (T-RFLP) analyses. PLFA analysis indicated that the soil microbial community composition was significantly different among the R. glutinosa with different years of monoculture. Compared with the newly planted soil, the total PLFA content and the ratio of bacteria/fungi in two-year monocultured soil greatly declined. Further analysis by T-RFLP also displayed the distinct differences in rhizospheric bacterial community structure of R. glutinosa. The microbial compositions from the wild and the newly planted R. glutinosa soils tended to be more similar. It was found that the bacteria including Proteobacteria and Firmicutes were predominant in the wild and newly planted R. glutinosa soils. Some beneficial biocontrol bacteria (such as Bacillus, Pseudomonas, etc.) gathered in the rhizosphere of the wild and newly planted R. glutinosa. However, a large number of pathogenic bacteria bred in the rhizosphere of the two-year monocultured R. glutinosa, such as Clostridium sp., Flexibacter polymorphus, and Clostridium ghoni, and the num-ber of beneficial bacteria and cellulose degradation bacteria decreased. Furthermore, qRT-PCR analysis verified that the total number of Pseudomonas was much higher in the wild and newly planted R. glutinosa soils than in the two-year monocultured soil. In conclusion, the pathogenic microbes breed seriously in the rhizospheric soil of wild R. glutinosa under the monoculture regime, and yet the number of beneficial bacteria decline, resulting in weakened ability of wild R. glutinosa to resist the diseases so that the two-year monocultured wild R. glutinosa grows abnormally and its yield is decreased drastically.