卫星搭载亚麻后代中PEG和NaCl

把空间生物学和细胞工程相结合,通过组织培养技术对其离体筛选,得到抗1.2% NaCl和35% PEG的愈伤组织。将所得抗性系愈伤组织在2.0 mg/L 6-苄基氨基嘌呤、0.5 mg/L吲哚乙酸的MS培养基上分化得到完整的植株。抗性系能在胁迫条件下保持高的生长速度和高效的脯氨酸合成能力。表明空间诱变与组织培养相结合有望可成为筛选抗胁迫变异系的有效途径。     

卫星搭载红豆草后代中耐盐细胞系的筛选及鉴定

将红豆草种子搭载于940703返地卫星,经田间繁殖得后代种子,先将种子在1.5%NaCl上筛选、并在该盐浓度下诱导愈伤组织和筛选,在无盐培养基上恢复生长后再在1.2%NaCl上筛选得到耐盐变异系.变异系具有正常的分化能力并表现出对PEG胁迫的交叉抗性.变异系在无胁迫条件下脯氨酸含量较低但在有盐胁迫时具有高效积累脯氨酸的能力.后者可能对红豆草耐盐系更为重要.变异系中脯氨酸的这种合成机理可能是由于一些基因在调控中对水的敏感性改变引起.梯度聚丙烯酰胺凝胶电泳表明耐盐系的SOD和酯酶分别出现175kD和75kD的新形式.说明空间诱变和组织培养相结合可以筛选耐盐变异系.     

苜蓿抗乙硫氨酸愈伤组织的筛选和特性

用乙硫氨酸为筛选剂,通过幼苗和组织培养筛选得到乙硫氨酸抗性愈伤组织。该愈伤组织在含乙硫氨酸的培养基上表现出较高的半抑制剂量和相对生长量。作为天门冬氨酸途径的产物,甲硫氨酸、异亮氨酸和赖氨酸在所筛选的愈伤组织中分别增加到对照的两倍多,但苏氨酸保持正常水平,另外酪氨酸、半胱氨酸和亮氨酸也有所增加,而在所筛选的愈伤组织中缬氨酸浓度却下降。说明在所筛选愈伤组织中存在一个以上与氨基酸合成相关的酶发生改变。同工酶分析表明,该愈伤组织中出现对照中没有的分子量为44kD的超氧化物歧化酶的分子量为45kD的酯酶谱带。     

红豆草抗羟脯氨酸变异系的筛选及其特性研究

通过选择-NaN_3诱变处理-再选择的程序从红豆草下胚轴愈伤组织获得了抗脯氨酸类似物L-羟脯氨酸的变异细胞系。抗性变异细胞系的游离脯氨酸含量比正常细胞系高4.6倍,并且抗性变异系亦表现出了很强的耐NaCl、PEG 能力。这可能为筛选抗逆境植物提供一条有效途径。     

水稻白叶枯病系和品种抗性鉴定的病性指标评价

从全国各病区筛选的１９个代表菌株,在三套（中国,日本和ＩＲＲＩ）１６个鉴别品种上进行测试,获得４个病情指标,即病斑长度,病组,日增速率和日增百分率,采用不同的的病情指标作方差分析,所得结果不完全一致;对４个病情指标进行相关及回归分析,结果表明,病情指标之间是存在显著的线性相关,且日增百分率为日增速率与病叶长度之商,这种相关性在主成分分析中也得到了证实,通过聚类分析发现,病斑长度不能与其它３个指标归     

苜蓿抗乙硫氨酸愈伤组织的筛选和特性

用乙硫氨酸为筛选剂,通过幼苗和组织培养筛选得到乙硫氨酸抗性愈伤组织。该愈伤组织在含乙硫氨酸的培养基上表现出较高的半抑制剂量和相对生长量。作为天门冬氨酸途径的产物,甲硫氨酸、异亮氨酸和赖氨酸在所筛选的愈伤组织中分别增加到对照的两倍多,但苏氨酸保持正常水平,另外酪氨酸、半胱氨酸和亮氨酸也有所增加,而在所筛选的愈伤组织中缬氨酸浓度却下降。说明在所筛选愈伤组织中存在一个以上与氨基酸合成相关的酶发生改变。同工酶分析表明,该愈伤组织中出现对照中没有的分子量为44kD的超氧化物歧化酶和分子量为45kD的酯酶谱带。     

拟南芥MeIAA抗性突变体的筛选和初步图位克隆分析

生长素是最重要的植物激素之一,参与了植物生长发育的各个方面。植物体内游离的IAA是生长素的主要活性形式,在IAA甲基转移酶1（IAMT1）的作用下,IAA可以转变为IAA甲酯（MelAA）。MelAA本身没有活性,在植物体内的MelAA酯解酶作用下可以重新转变为IAA。MelAA是非极性分子,能够在植物体内自由扩散。利用MelAA的这种特殊性质筛选突变体,可以分离到MelAA代谢途径或者IAA途径中新的成分。我们对拟南芥种子进行EMS诱变,通过观察黑暗下下胚轴的生长情况,筛选MelAA的抗性突变体。我们成功分离到了8株可能的抗性突变体,并对其中的一个Methyl-JAAresistant1（mir1）突变体进行了深入分析。MelAA抗性突变体的筛选将为进一步了解MelAA的代谢、IAA稳态调控和响应机理提供新的材料。     

拟南芥 MeIAA 抗性突变体的筛选和初步图位克隆分析

生长素是最重要的植物激素之一, 参与了植物生长发育的各个方面。植物体内游离的IAA是生长素的主要活性形式, 在IAA甲基转移酶1(IAMT1)的作用下, IAA可以转变为IAA甲酯 (MeIAA)。MeIAA本身没有活性, 在植物体内的MeIAA酯解酶作用下可以重新转变为IAA。 MeIAA是非极性分子, 能够在植物体内自由扩散。利用MeIAA的这种特殊性质筛选突变体, 可以分离到MeIAA代谢途径或者IAA途径中新的成分。我们对拟南芥种子进行EMS诱变, 通过观察黑暗下下胚轴的生长情况, 筛选MeIAA的抗性突变体。我们成功分离到了8株可能的抗性突变体, 并对其中的一个Methyl -IAA resistant 1 (mir1) 突变体进行了深入分析。MeIAA抗性突变体的筛选将为进一步了解MeIAA的代谢、IAA稳态调控和响应机理提供新的材料。     

拟南芥MelAA抗性突变体的筛选和初步图位克隆分析

生长素是最重要的植物激素之一,参与了植物生长发育的各个方面。植物体内游离的IAA是生长素的主要活性形式,在IAA甲基转移酶1（IAMT1）的作用下,IAA可以转变为IAA甲酯（MelAA）。MelAA本身没有活性,在植物体内的MelAA酯解酶作用下可以重新转变为IAA。MelAA是非极性分子,能够在植物体内自由扩散。利用MelAA的这种特殊性质筛选突变体,可以分离到MelAA代谢途径或者IAA途径中新的成分。我们对拟南芥种子进行EMS诱变,通过观察黑暗下下胚轴的生长情况,筛选MelAA的抗性突变体。我们成功分离到了8株可能的抗性突变体,并对其中的一个Methyl-JAAresistant1（mir1）突变体进行了深入分析。MelAA抗性突变体的筛选将为进一步了解MelAA的代谢、IAA稳态调控和响应机理提供新的材料。     

In vitro selection for salt tolerant lines in Lycopersicon peruvianum

A salt-tolerant callus line of Lycopersicon peruvianum has been obtained by exposing the cells, in suspension cultures and then in callus, to increasing concentrations of NaCl (50–350mM). This selected line grew better than the nonselected line at all levels of NaCl. Moreover, this selected line grew better in media containing salt than in those without it. It retained its tolerance after subculture for 3 passages (3 months) on salt-free medium. The growth of the selected line in mannitol was similar to that of the nonselected line, which suggested that the superiority of the selected line under salt stress was not due to osmotic stress tolerance. The ions SO ₄ ^–– and K⁺ were highly toxic to L. peruvianum root callus, while Na⁺, Mg⁺⁺ and Cl^– were less toxic.     

In vitro recurrent selection of potato: production and characterization of salt tolerant cell lines and plants

A stable salt-tolerant potato cell line, able to grow on media containing 60–450 mM NaCl (i.e. low to high salinity) was selected. Callus grown on 120 or 150 mM NaCl showed higher fresh weights than the rest of the treatments. Replacing NaCl by KCl or Na2SO4 showed that reductions in fresh weight were mainly due to the presence of Na+ ions. When PEG 6000 was added to the medium instead of salt, the salt tolerant cell lines were unable to overcome the PEG-induced water stress. Whole plants, regenerated from salt tolerant callus, exhibited salt stress tolerance as evidenced by their higher fresh and dry weights when watered with 90 mM NaCl, and they also produced more tubers per plant under salt stress. Salt-tolerant plants differed phenotypically from control plants both in terms of leaf shape, tuber flesh and skin colour, which was reddish. In addition, DNA fingerprinting by RAPDs, with 70 different primers, confirmed that the salt tolerant regenerants also differed genotypically from the control, salt sensitive Kennebec potato plants from which they had been selected. This revised version was published online in June 2006 with corrections to the Cover Date.     

Characterization of salt tolerant alfalfa (Medicago sativa L.) plants regenerated from salt tolerant cell lines

Salt tolerant cell lines have been selected from Medicago sativa, by a single step selection process on tissue culture medium containing 1% NaCl. Plants regenerated from these lines show improved salt tolerance compared to parent plants. The regenerated plants are vigorous, have flowered and are self fertile. The cellular salt tolerance characteristic can be passaged through the regenerated plants, since callus cultures initiated from immature ovaries of the salt tolerant regenerated plants are salt tolerant without additional selection on 1% NaCl. Several of these second generation callus cultures have been regenerated to produce vigorous plants which maintain the salt tolerance characteristic. The tolerance phenotype appears dominant in seeds obtained from self fertilization of the tolerant plants. The regenerated salt tolerant plants are therefore a valuable source as genotypes in plant breeding for salt tolerance and isolation, identification and manipulation of genes which confer salt tolerance in alfalfa.Abbreviations SH Schenk and Hildebrandt medium - 2,4-D 2,4-dichlorophenoxyacetic acid     

小麦耐盐细胞系及后代耐盐稳定性的生化分析

以离体培养筛选出的耐盐小麦变异系及其后代为材料,对其耐盐稳定性进行有关生理生化特性分析。结果表明：（１）随着耐盐愈伤组织耐盐能力的提高,过氧化物同工酶酶带谱加,与对照相比,三个区域出现了明显差异;（２）从耐盐愈伤组织酯酶同工酶酶谱发现,耐盐愈伤组织具有Ｃ２,Ｃ５,Ｃ９,Ｃ１１新增加酶带;（３）耐盐系后代幼苗能维持较高的Ｋ＾＋／Ｎａ＾＋比值,在盐浓度为０．９％时,其Ｋ＾＋／Ｎａ＾＋为０．７８８,而对     

In vitro selection and characterization of polyethylene glycol (PEG) tolerant callus lines and regeneration of plantlets from the selected callus lines in sugarcane (Saccharum officinarum L.)

A system for in vitro selection of drought tolerant callus lines in sugarcane was developed. High molecular weight PEG was used as selective agent. Selected callus line grew better than non-selected callus when grown on different concentrations of PEG. The activity of antioxidant enzymes like CAT, POX, APX and SOD were high in selected callus than in non-selected callus. Osmolytes like proline and ascorbic acid were at higher levels in selected callus than in non-selected callus, however at higher concentrations (20–30 %) of PEG, levels of proline and ascorbic acid decreased. The frequency of organogenesis and number of plantlets decreased in selected callus than in non-selected callus. The results can be used for in vitro screening and manipulations of sugarcane for improvement of drought tolerance     

In vitro characterization of salt stress effects and the selection of salt tolerant plants in rice (Oryza sativa L.)

Summary The response of plant cells to salt stress was studied on embryo derived calli of rice (Oryza sativa L.) in order to identify cellular phenotypes associated with the stress. The feasability of selecting salt tolerant callus and its subsequent regeneration to plants was also studied. Callus was grown on agar-solidified media containing 0%, 1% and 2% (w/v) NaCl for 24 days. Parameters such as fresh weight, dry weight, soluble protein and proline content were measured. The callus growth decreased markedly with increasing NaCl concentration in the medium. The proline content was enhanced several fold in salt stressed calli. A prolonged exposure of callus to the salt environment led to discolouration and arrested growth in the majority of the calli and only a small number of callus cells maintained healthy and stable growth. These variants were subcultured every three weeks for a period of four months onto medium containing 1% NaCl to identify tolerant lines. At the end of the third cell passage, the tolerant calli were transferred to regeneration medium to regenerate plants. The regeneration frequency in the salt-selected lines was enhanced when compared to unselected lines.     

In vitro culture of cells and tissues from the mosquito,Anopheles quadrimaculatus say

Summary Tissues and cells from various life stages and ages ofAnopheles quadrimaculatus were cultured in several media. Pupal tissue maintained in Schneider's (1) medium was the most successful system. These cells remained viable for 210 days. Xix morphologically distinguishable cell types were observed: spherical cells, two type of neuronlike cells, musclelike cells, epithelial-like cells, and polymorphic cells.     

In vitro selection and characterization of Ni-tolerant callus lines of Setaria italica L

Nickel tolerant callus lines of Setaria italica L. were developed from callus cultures grown on MS medium supplemented with 0.5 mg·dm⁻³ kinetin+2.0 mg·dm⁻³ 2,4-D+2.0 mg·dm⁻³ Ni⁺². Standard growth parameters such as callus fresh and dry weight, growth tolerance index were used as indicators of nickel toxicity. Measurements as early as 2 weeks after the beginning of the treatments did not yield consistent results. However, growth tolerance index at 4, and 8 weeks after the beginning of treatments yielded significant differences among the non-tolerant and tolerant calli. The tolerant calli has enhanced growth at 2.0 mg·dm⁻³ Ni⁺² while non-tolerant calli showed a reverse trend in growth in the presence of 2.0–2.5 mg·dm⁻³ of nickel. The tolerant calli differentiated into mass of embryogenic calli within 4 weeks of culture which could be maintained for prolonged period without loss of regenerative capacity.