茶条槭愈伤组织的再生体系建立及其没食子酸含量的测定

通过愈伤组织诱导途径,建立了快速高效的茶条槭再生体系。成熟种子在MS＋1．0mg·L^-1 6-BA的培养基中萌发,以茎段作为外植体,在WPM＋0．002-0．01mg·L^-1 TDZ＋0．1mg·L^-1 6-BAR培养3周诱导形成愈伤组织,诱导频率平均为98．0％。愈伤组织转入WPM＋0．01mg·L^-1 TDZ＋0．1mg·L-^1 6-BA培养基中得到再生芽,分化频率为42．0％,平均每块愈伤产生再生芽10个左右。转到WPM＋0．3mg·L^-1 IBA的培养基上的再生芽均可生根并长成完整植株,小苗移栽成活率达到89．0％。实验还建立了愈伤组织中没食子酸的提取和HPLC检测方法。对深绿色愈伤组织连续培养2个继代后,没食子酸含量达到2．8％。     

不同生长调节剂对丹参快速繁殖的影响

探讨了丹参(Salvia miltiorrhiza Bunge)快速繁殖过程中不同生长调节剂的影响.实验表明:MS 6-BA 2.0mg/L NAA 0.05 mg/L是诱导初代培养的芽产生大量丛生芽的最佳培养基,其诱导生芽率为100%;最佳的丛生芽增殖培养基为MS 6-BA 1.0 mg/L NAA 0.01 mg/L,其增殖倍数为15倍;MS 6-BA 0.5～2.0 mg/L是诱导大量不定芽的最佳培养基,其诱导生芽率为100%,最佳的不定芽增殖培养基为MS 6-BA 1.0 mg/L,其增殖倍数为24倍;诱导生根较好的培养基为1/2MS IBA 0.1 mg/L,生根率为98%,移栽成活率为100%.     

Kinetic and structural insight into the mechanism of BphD, a C-C bond hydrolase from the biphenyl degradation pathway

Kinetic and structural analyses of 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid (HOPDA) hydrolase from Burkholderia xenovorans LB400 (BphD(LB400)) provide insight into the catalytic mechanism of this unusual serine hydrolase. Single turnover stopped-flow analysis at 25 degrees C showed that the enzyme rapidly (1/tau(1) approximately 500 s(-1)) transforms HOPDA (lambda(max) = 434 nm) into a species with electronic absorption maxima at 473 and 492 nm. The absorbance of this enzyme-bound species (E:S) decayed in a biphasic manner (1/tau(2) = 54 s(-1), 1/tau(3) = 6 s(-1) approximately k(cat)) with simultaneous biphasic appearance (48 and 8 s(-1)) of an absorbance band at 270 nm characteristic of one of the products, 2-hydroxypenta-2,4-dienoic acid (HPD). Increasing solution viscosity with glycerol slowed 1/tau(1) and 1/tau(2) but affected neither 1/tau(3) nor k(cat), suggesting that 1/tau(2) may reflect diffusive HPD dissociation, and 1/tau(3) represents an intramolecular event. Product inhibition studies suggested that the other product, benzoate, is released after HPD. Contrary to studies in a related hydrolase, we found no evidence that ketonized HOPDA is partially released prior to hydrolysis, and, therefore, postulate that the biphasic kinetics reflect one of two mechanisms, pending assignment of E:S (lambda(max) = 492 nm). The crystal structures of the wild type, the S112C variant, and S112C incubated with HOPDA were each determined to 1.6 A resolution. The latter reveals interactions between conserved active site residues and the dienoate moiety of the substrate. Most notably, the catalytic residue His265 is hydrogen-bonded to the 2-hydroxy/oxo substituent of HOPDA, consistent with a role in catalyzing ketonization. The data are more consistent with an acyl-enzyme mechanism than with the formation of a gem-diol intermediate.     

Numerical modelling of nanoparticle deposition in the nasal cavity and the tracheobronchial airway

Recent advances in nanotechnology have seen the manufacture of engineered nanoparticles for many commercial and medical applications such as targeted drug delivery and gene therapy. Transport of nanoparticles is mainly attributed to the Brownian force which increases as the nanoparticle decreases to 1 nm. This paper first verifies a Lagrangian Brownian model found in the commercial computational fluid dynamics software Fluent before applying the model to the nasal cavity and the tracheobronchial (TB) airway tree with a focus on drug delivery. The average radial dispersion of the nanoparticles was 9x greater for the user-defined function model over the Fluent in-built model. Deposition in the nasal cavity was high for very small nanoparticles. The particle diameter range in which the deposition drops from 80 to 18% is between 1 and 10 nm. From 10 to 150 nm, however, there is only a small change in the deposition curve from 18 to 15%. A similar deposition curve profile was found for the TB airway.     

江西省森林碳蓄积过程及碳源/汇的时空格局

森林碳蓄积是研究森林与大气碳交换以及估算森林吸收或排放含碳气体的关键参数,不同年龄森林的碳源/汇功能差异则体现出森林生态系统碳蓄积过程的时间特征。以森林资源清查的样方数据作为数据源,通过刻画主要树种的林分蓄积生长曲线、林龄与净初级生产力(NPP)之间的关系,驱动区域碳收支模型(InTEC)模拟江西省1950—2008年的森林碳蓄积过程,了解山江湖工程实施以来的森林碳源/汇状况。结果表明,20世纪80年代以前,江西省森林年平均NPP波动于450—813 gCm-2a-1之间,年净增生物量碳26.55—36.23 TgC/a,年净增木质林产品碳0.01—0.3 TgC/a;80年代初,NPP和年净增生物量碳分别降至307.39 gC m-2a-1和17.31 TgC/a,而年净增木质林产品碳却高达0.6 TgC/a,说明森林被大量砍伐进入林产品碳库;1985年山江湖工程实施后,大面积造林使得年净增碳蓄积呈现急剧上升趋势,生物量和木质林产品碳蓄积分别上升至目前的42.37 TgC/a和0.79 TgC/a,而平均NPP值增加缓慢、碳汇功能降低,说明林分质量有待提高;90年代后碳汇功能开始稳步增强,说明造林面积的迅速增加是引起江西省森林碳增汇的主要驱动因素,但未来森林增汇潜力应源于森林生长和有效的经营管理。     

温湿度对中华通草蛉越冬成虫存活的影响

室内研究了不同温湿度对中华通草蛉 (Chrysoperla sinica)越冬成虫存活的影响。试验采用因子二次正交旋转组合设计的要求安排 ,研究了越冬成虫在不同的温度组合条件下储存不同时间后的存活率 ,并得到了在不同时间后 ,成虫存活率与温湿度间的二次回归模型。结果表明 ,在试验条件下 ,越冬成虫存活的最佳条件组合是温度为 5℃和相对湿度为 75 % ,此条件下储存90 d的越冬成虫存活率达 85 %以上 ;温度对成虫存活率的影响最大 ,湿度次之 ,温湿度的交互作用最不重要。利用温湿度与存活率之间的回归方程 ,分析并得出了适宜于越冬中华通草蛉成虫存活的条件为温度 5～ 9℃ ,相对湿度 70 %～ 85 % ,温度和湿度过高或过低均不利于成虫的存活     

Flavonoid compound breviscapine suppresses human osteosarcoma Saos‐2 progression property and induces apoptosis by regulating mitochondria‐dependent pathway

This study was aimed to investigate the ability of a flavonoid compound breviscapine (BVP) to suppress growth and elicit apoptosis in human osteosarcoma (OS) Saos‐2 cells. The cells were cultured in vitro and treated with three concentrations of BVP (80, 160, and 320 μg/ml). Moreover, C57 mice were injected with Saos‐2 cells to establish a subcutaneous xenograft model, and they were subsequently treated with three doses of BVP via intraperitoneal injection. The viability of the cells was examined by the Cell Counting Kit‐8 method. The apoptotic cells were assessed by flow cytometry and terminal deoxynucleotidyl transferase dUTP nick end labeling staining. The tumor volume and weight were monitored from day 3 through day 21 after the last injection. The expression of bax, bcl‐2, and cytochrome c (cyt c) mRNA was detected by a real‐time polymerase chain reaction. The protein levels of bax, bcl‐2, cyt c, caspase 3, and caspase 9 were evaluated by Western blot. The expression and distribution of bcl‐2 and bax in tissues were detected by immunohistochemistry. Compared with the control group, BVP treatment inhibited cell proliferation and induced apoptosis of Saos‐2 cells in vitro. Consistently, treatment of mice bearing transplanted tumors with BVP suppressed the growth of OS tumors and promoted cell apoptosis; it also reduced tumor volume and weight. Mechanistically, BVP‐induced apoptosis was mediated by the mitochondria‐dependent pathway, as evidenced by the increased expression of bax and cyt c and the decreased expression of bcl‐2, as well as activation of caspase 9 and caspase 3 in vitro and in vitro. Collectively, BVP inhibits growth and promotes apoptosis of OS by activating the mitochondrial apoptosis pathway.