抗白粉病胡麻种质资源田间鉴定与筛选

白粉病目前已成为影响胡麻产量和质量最常见的病害之一, 种植抗病品种是防控病害最经济环保的有效措施, 然而抗病亲本材料的缺乏已成为制约抗病品种选育的关键因素。为筛选出抗白粉病胡麻材料, 本研究在田间自然感病的条件下, 采用病情指数法对300份国内外胡麻种质资源材料进行了抗白粉病鉴定和评价。结果表明, 所有供试材料均程度不同地感染胡麻白粉病, 无免疫材料, 仅有5份材料为中抗; 其余295份均为感病材料, 其中8份材料中感, 52份材料感病, 235份材料高度感病。本研究可为抗白粉病胡麻品种的培育及相关抗病基因的发掘提供参考。     

普通小麦抗白粉病配合力及其与过氧化物酶的关系

选用6个亲本组配成双列杂交设计,对普通小麦抗白粉病的配合力及基因效应进行了分析。结果表明,白粉病病情指数属于数量性状遗传,符合加性—显性遗传模型,由加性效应和非加性效应共同控制,且以加性效应为主。低病情指数为部分显性。不同亲本之间一般配合力效应及含有的有利显性基因数存在明显差别。因此,选配杂交组合应在一般配合力高的基础上,注重其特殊配合力的选择。研究还表明,感病品种过氧化物酶活性高。     

感染白粉病小麦叶片细胞的超微变化

小麦感染白粉病菌后,叶片叶绿体肿胀,双层膜不完整或消失,基粒片层排列疏松紊乱,细胞中出现许多由单层膜围成的大小不等的空胞和类似纤维状的膜状物,细胞核膜消失,质壁分离.     

月季抗白粉病资源的筛选

通过对月季11个品种的抗白粉病鉴定，筛选出5个免疫品种、1个高抗品种（HR）、2个中抗品种（MR）、3个高感品种（HS）。     

小麦远缘杂交后代节燕98-2分离类型贮藏蛋白的研究

采用A-PAGE和SDS-PAGE聚丙烯酰胺凝胶电泳方法,对远缘组合分离出来的节燕98-2类型入选11个遗传性基本稳定的具有高产、多抗的小麦株系的醇溶蛋白和高分子量谷蛋白亚基进行了分析.结果表明,在A-PAGE电泳分析中,11个供试株系具有11种不同的醇溶蛋白带型.在SDS-FAGE电泳分析中,出现了7种不同的高分子量谷蛋白亚基(HMW-GS)及6种亚基组合类型,优质亚基及亚基组合所占的比例较少,品质评分偏低,其变幅为5～8分,平均为6.36分.但在所分析的材料中,出现了一个少见的特殊亚基:2 10 12.并研究了这些HMW-GS和组合频率及特点.11个株系中7个具有45 10优质亚基和2个具有2*亚基,它们可供小麦优质育种利用.研究表明,通过远缘杂交能够选育出具有高产、抗病和优质的小麦新材料.     

黄瓜抗霜霉病异源易位系CT201的筛选与鉴定

 将栽培黄瓜‘北京截头’ (Cucumis sativus L. , 2n = 14) 与Cucum is属双二倍体新种C. hytivus (2n = 38) 回交, 随后自交。通过霜霉病田间接种试验筛选, 从中发现抗霜霉病单株HH12825。将HH12825与C. hytivus的原始亲本‘北京截头’和野生种C. hystrix进行农艺性状对比观察, 发现此单株在叶面积、节长、果长×果径等方面介于栽培黄瓜和野生种之间, 在侧枝数、果刺颜色等方面偏向野生种。观察其花粉母细胞减数分裂过程, 发现其PMC中期Ⅰ多价体频率(56% ±8% ) 和后期Ⅰ二价体分离滞后率(72% ±5% ) 都较高, 具有染色体易位的细胞学特征。进一步利用RAPD分子标记分析, 结果在40个随机引物中找到了两个引物( E219: ACGGCGTATG和A I220: CCTGTTCCCT) 能够在HH12825中重复地扩增出原始亲本野生种C. hystrix特异DNA片断, 从分子水平上证明了其为黄瓜异源易位系, 并把此易位系命名为CT201。     

黄瓜白粉病抗性遗传机制的研究

 采用多世代联合分析方法, 通过3个抗感杂交组合研究了黄瓜白粉病抗性的遗传规律。结果表明, 3个组合的最适遗传模型皆是两对加性- 显性- 上位性主基因+加性- 显性- 上位性多基因模型(E2120模型) 。组合Ⅰ的主基因遗传率为64.26% ～95.47% , 两对主基因感病相对抗病为部分显性, 两主基因的加性效应及第二主基因的显性效应较大, 两主基因的加性×显性互作效应也较大。组合Ⅱ和组合Ⅲ两主基因的遗传率分别为95.35%和96.04% , 两主基因的加性效应、显性效应和显性度较为相近。     

中国香瓜与菜瓜地方品种资源白粉病抗性评价

春秋2个季节在温室利用风媒接种方法对搜集的102份香瓜和14份菜瓜种质资源进行了白粉病抗性评价,结果鉴定出7份香瓜和1份菜瓜高抗白粉病,其病情指数为零,1份菜瓜抗病,其病情指数0.9,表明我国香瓜和菜瓜地方品种资源中蕴涵着潜在的改良甜瓜白粉病抗性的基因资源。     

Differential effects of -mannose and 2-deoxy- -glucose on attempted powdery mildew fungal infection of inappropriate and appropriate ramineae

Barley, oat and wheat were used as both inappropriate hosts (IH) and appropriate hosts (AH) for three formae speciales of the fungus Blumeria graminis, the causal agent of powdery mildew disease. Treatment with either the glucose analog 2-deoxy- -glucose (DDG) or with -mannose dramatically suppressed penetration resistance in IH and to a much lesser extent in AH combinations. Other effects of DDG and -mannose were strikingly dissimilar. DDG greatly reduced localized autofluorescence at fungal attack sites on epidermal cells, and prevented hypersensitive epidermal cell death (HR). -mannose had little effect on autofluorescence or HR. DDG arrested the development of fungal haustoria and apparently prohibited biotrophy leading to secondary hyphae. -mannose allowed haustorial development and functional biotrophy leading to the production of elongating secondary hyphae. This suggests that B. graminis is in some way capable of utilizing -mannose as a carbon substrate. Results with IH combinations paralleled those of known mlo -barley responses to DDG and -mannose. Results are discussed in relation to specific physiological processes known to be influenced by either DDG or by -mannose, or by both compounds.     

Evidence that a Leaf-Disk Test Allows Assessment of Isolate-Specific Resistance in Brassica oleracea Crops Against Downy Mildew (Peronospora parasitica)

A rapid resistance/susceptibility test for Peronospora parasitica (downy mildew) was established by inoculating leaf-disks of four Brassica oleracea accessions. Several conditions were tested: disk disinfection or not, agar medium with or without nutrients and with 50 or 100 ppm of benzimidazole. Using disinfected disks placed on agar (no nutrient and benzimidazole at 50 or 100 ppm), the responses of leaf-disks to four isolates were similar to those obtained using the classical cotyledon test, whereas undesired contaminations occurred in all other conditions. The possible effect of the particular leaf used for obtaining the disks was also studied. In each incompatible interaction tested, disks were resistant whatever the leaf used. In compatible interactions, susceptible phenotypes were observed on disks derived from the six lowest leaves, but disks from upper leaves were resistant. The genetic basis of resistance in a F1 hybrid broccoli was assessed, by testing six isolates on an F2 population derived from this hybrid. The cotyledon test only allows inoculation of two isolates per seedling, whereas many isolates can be tested on each plant by using leaf-disks. The segregation of the resistance to each of the six isolates was analysed: two dominant genes (tightly linked) control resistance to all isolates (one to five isolates; the other to only one isolate).