大花君子兰叶绿体基因组及其特征

采用Illumina MiSeq测序平台对大花君子兰（Clivia miniata）叶片总DNA进行测序，通过组装获得了其叶绿体基因组（cpDNA）全长序列（158 114 bp）。对其cpDNA注释得到135个基因，包含87个蛋白编码基因、40个tRNA基因和8个rRNA基因。采用生物信息学方法对获得的cpDNA进行简单序列重复（SSR）分析和密码子偏好性分析。结果显示：①大花君子兰cpDNA中共有61个SSR位点，其中单核苷酸、二核苷酸、三核苷酸、四核苷酸、五核苷酸和六核苷酸重复数分别为38、9、2、8、3和1个，多数SSR分布在基因间隔区；②大花君子兰cpDNA密码子偏爱以A或U（T）结尾，亮氨酸使用频率最高，半胱氨酸使用频率最低。基于24种植物的cpDNA全长和23种植物的叶绿体ycf2基因序列进行系统发育分析，结果显示大花君子兰与石蒜科植物在同一分支，显示最近的亲缘关系，支持大花君子兰属于石蒜科。基于叶绿体ycf2的系统发育分析结果与基于cpDNA全长的系统发育分析研究结果大部分相同，支持ycf2基因可以代替cpDNA全长用于植物系统发育分析。     

High frequency embryogenic callus induction and plant regeneration from mature caryposis of big bluestem and little bluestem

Big bluestem (Andropogon gerardii Vitman) and little bluestem [Schizachyrium scoparium (Michaux) Nash.] are native to the North America and are important forage grasses and ornamental grasses. Both grasses are proposed as ideal biomass producers for cellulosic ethanol production. To apply genetic transformation, which is an important tool for incorporating desirable agronomic traits into plants to both species, however requires an efficient and reproducible regeneration protocol. We used mature caryopses from big and little bluestem as explants and tested the effect of various combinations of 2, 4-dichlorophenoxyacetic acid (2, 4-D) (1, 2, 3, 4 or 5 mg l⁻¹) and kinetin (KT) (0, 0.1 or 0.2 mg l⁻¹) on embryogenic callus induction with LS as the basal medium. The highest percentage of embryogenic calli induction occurred on medium containing 2, 4-D alone at 2 mg l⁻¹ for ‘Bison’ and on medium containing 4 mg l⁻¹ 2, 4-D alone for ‘Bonilla’ big bluestem. For little bluestem, the highest percentage of embryogenic callus induction occurred on medium containing 3 mg l⁻¹ 2, 4-D plus 0.1 mg l⁻¹ kinetin, suggesting that addition of KT is beneficial. Shoot regeneration took place on LS basal medium without any plant growth regulator for both species, although the addition of KT increased both regeneration frequency and the number of shoots produced per callus. Rooting of shoots reaching about 2 cm long occurred readily with or without α-naphthaleneacetic acid (NAA). Rooted plantlets were all successfully established in the soil.     

柑橘幼果发育期碳水化合物代谢及其与生长发育的关系

温州蜜柑幼果在盛花后逐渐生长 盛花后6 d开始大量脱落 日本甜夏橙幼果在盛花后12 d内重量未增加，一直处于急剧落果期。甜夏橙幼果中蔗糖含量高出温州蜜柑20多倍，种间还原糖含量变化趋势略有不同。两种柑橘的淀粉含量变化也不同，但它们的淀粉含量与淀粉酶活性、幼果相对脱落率均呈负相关。对幼果碳水化合物代谢与生长、脱落的关系作了讨论。     

焦锑酸钾沉淀法定位Ca~(2+)在梨生理研究中的应用

介绍了应用焦锑酸钾沉淀法定位Ca2＋的方法，以及在梨生理研究中的具体步骤和应用效果。结果表明：在固定液中加焦锑酸钾处理进行制样，梨树不同器官或组织细胞中的自由态Ca2＋，都能生成焦锑酸钙在原部位沉淀，经染色后在电子显微镜下呈现出黑色颗粒，而固定液中不加焦锑酸钾处理的则没有这种颗粒。再进一步用Ca2＋的专一性鳌合物EGTA进行处理，检查这些黑色颗粒是否消失，以证实黑色颗粒就是Ca2＋，从而可对Ca2＋进行定位标记。在不同的组织细胞及同一组织细胞在不同的生理时期，其被标记的Ca2＋密度和场所是不同的，可通过其动态变化来探讨它的作用机理。还对用此方法定位Ca2＋的注意事项进行了讨论。     

萘乙酸对大白菜钙素吸收运转及防治干烧心病的研究

本研究从补钙入手,探索防治干烧心病的方法。用0.7％CaCl_2·2H_2O对和50ppmNAA混合液在大白菜结球期叶面喷洒5次,经8年试验,对大白菜干烧心病的相对防治效果达80％以上。 在此基础上,采用~(45)Ca示踪试验的方法对防病机理做了进一步研究。结果表明,无论从根部还是从叶部加萘乙酸对根部和叶部~(45)Ca的吸收和运转均具有促进作用,并且改变了其在大白菜植株内的分配规律。对照株单位干叶重dpm值自外向内呈下降趋势(130×10~3─60×10~3);用NAA处理株则相反,自外向内呈增加趋势(120×10~3─250×10~3),说明萘乙酸具有促进钙素向叶球中内部运转的功效。这种效果在贮藏期间仍能保持。另外,~(45)Ca向直接受到NAA处理部位的运转量有明显增高的趋势。这一结果为补钙防治干烧心病提供了理论依据。     

姜片虫虫体抗原氨基酸的测定

本文报道4种方法制备姜片虫虫体抗原,进行氨基酸组成的测定。其氨基酸总量(mg/100ml)结果显示:Ag-F1:608.50;Ag-F2:645.80;Ag-F3:357.14;Ag-F4:501.40;以 Ag-F3总量为最低,但值得重视的是 Ag-F3的丙氨酸(8.34),组氨酸(8.60),甘氨酸(11.00);苏氨酸(12.00),均显著降低。而 Ag-F4的组氨酸(4.80)为17种氨基酸含量最低者。其原因有待探讨。     

套袋对红富士苹果色素及糖、酸含量的影响

 以苹果(Malus pumila) ‘长富2’品种为试材, 研究了套袋对果皮色素及果肉糖、酸含量的影响。结果表明, 套袋果果皮色素、可溶性糖、可滴定酸具有同对照果基本相同的消长规律, 但含量均始终低于对照; 摘袋后果实可溶性糖含量迅速升高, 且花青苷积累速度明显快于对照; 套袋主要降低了果实中山梨醇和蔗糖的含量, 果糖和葡萄糖降低幅度相对较小。     

钙、萘乙酸对亚精胺在猕猴桃贮藏期间作用效果的影响

以5年生中华猕猴桃品系(湘源81-2)为试材,进行了果实采收后Spd(亚精胺)、Spd+Ca2+、Spd+NAA浸果处理,研究钙、萘乙酸对多胺作用效果的影响。结果表明:不同处理均不同程度地抑制了果实的呼吸强度、果肉PG活性和细胞膜透性的增加,其中Spd+NAA浸果处理的作用效果最为显著,贮藏68d时,果肉硬度最高(0.259MPa),软果率较低(79%),好果率达100%;其次为Spd处理。     

Changes of Ca2＋ activated potassium channels and cellular-proliferation in autogenous vein grafts

AIM: To investigate changes of Ca^2＋ activated potassium channels (K_Ca) in autogenous vein grafts. METHODS: The contraction of venous ring was measured by means of perfusion in vitro. The intimal proliferation and proliferation of cultured smooth muscle cells (vascular smooth muscle cells, VSMCs) were observed by the means of computerised image analysis and MTT method, respectively. Furthermore, whole cell mode of patch clamp was used to record K_Ca of VSMCs isolated from autogenous vein grafts. RESULTS: 1 week after transplantation there were no significant differences of contraction and intimal relative thickness between autogenous vein grafts and control. Contraction and intimal relative thickness of autogenous vein graft were significantly increased 2 weeks after transplantation (P＜0.05, n=8 vs control), and they were more enhanced 4 weeks after vein transplantation (P＜0.01, n=8 vs control). TEA (blocker of Ca^2＋ activated potassium channels) increased MTT A₄₉₀ value of VSMCs from femoral vein in a dose-dependent manner (P＜0.05, n=8). K_Ca current density was significantly attenuated in VSMCs from autogenous vein grafts 1-4 weeks after transplantation (P＜0.05, n=5). CONCLUSION: K_Ca was inhibited in autogenous vein graft, which accounted for vasospasm and intimal proliferation.     

Chloride channels of platelets

Chloride channels distribute widely in the body, and participate in many physiological actions and regulatory processes. Based on their physiological roles and molecular structures, six kinds of chloride channels have been identified: (1) The chloride channels family; (2) Cystic fibrosis transmembrane conductance regulator; (3) Swelling-activated chloride channels; (4) Calcium-activated chloride channels; (5) The p64 (CLIC) gene family; (6) γ-aminobutyric acid and glycine receptors. The chloride channels do exist in platelets, and their appearances are dependent on the presence of intracellular calcium. Blocking agents of chloride channels inhibit the thrombin-activated platelet aggregation and the elevation of the intracellular calcium concentration in a dose-dependent manner. It is suggested that chloride channels play a role in the activation of platelets. In addition, chloride channels act on both the cell volume regulation and the intracellular pH regulation in platelets.