两种罗氏培养基的临床应用比较

目的 分析ＷＨＯ 推荐的无淀粉ＬＪ培养基应用的可行性。方法 将无淀粉ＬＪ培养基与改良ＬＪ培养基做比较， 分别从结核菌的分离率、生长速度及药物敏感试验等方面观察。结果 两种培养基应用于结核菌培养的初代分离率无显著差异（ Ｐ＞ ０－０５） ， 生长速度基本接近， 药物敏感试验总相关率为９７－３ ％ 。结论 改良ＬＪ培养基的配制可以不加马铃薯淀粉。

霍乱肠毒素分离方法的改进

用作者改进的液体培养基在5%CO_2环境中培养霍乱弧菌(Inaba 569B),每ml培养滤液可获得霍乱肠毒素(CT)1.215～2.012μg。在分离提纯CT时,先用DEAE-Sephadex A_(50)除去大部分色素及杂蛋白,再用Sephacryl S_(-200)分纯,效果好,重复性强;其第Ⅰ组分即为CT,肠襻试验阳性,双向琼脂扩散试验及HPLC检测结果均与上海CT一致。分子量为86000。

丰花月季组培快繁技术研究初报

组培快繁技术研究结果表明 :适宜丰花月季离体芽诱导分化的培养基为 MS+6 - BA0 .5 0 mg/L+NAA0 .1 0～ 0 .2 0 mg/L ;适宜丛生芽继代增殖的培养基为 MS+6 - BA1 .0 0 mg/L +NAA0 .1 0～ 0 .2 0 mg/L ;适宜丰花月季试管苗生根的培养基为 1 /2 MS+NAA 0 .1 0 mg/L ,其生根率达 90 %

Study on Multiplication, Rooting and Transplanting of Tissue Culture Plantlets of Rhododendron chrysanthum Pall

[Objective] This study aimed to shorten the multiplication culture and root- ing culture periods of Rh. chrysanthum Pall. [Method] The Rh. chrysanthum Pall tis- sue culture plantlets collected from Changbai Mountain were used as material, and the effects of different hormone combinations and coconut milk on the proliferation and differentiation of Rh. chrysanthum Pall tissue culture plantlets were investigated. In addition, the rooting medium and transplanting matrix for Rh. chrysanthum Pall tissue culture plantlets were explored. [Result] The medium composed of modified MS, iBA （3 mg/L） and ZT （1.5 mg/L） was the optimum medium for subculture mul- tiplication of Rh. chrysanthum Pall tissue culture plantlets. The multiplication multiple and average plant height were significantly improved by adding coconut milk into the medium （150 mg/L）. [Conclusion] For Rh. chrysanthum Pall tissue culture plantlets, the optimum rooting culture medium was composed of modified MS （1/4） and IBA （5.0 mg/L）, and the tissue culture plantlets began to root 8 d after the inoculation. The root induction treatment was carried out after a 15-d sand culture, and the suitable matrix was composed of tufty soil, humus soil and perlite （2：1：1） with a survival rate of 95.66%.

Analysis of the Biological Characteristics of a Parasitical Fungus in Chrysosplenium absconditicapsulum J. T. Pan Leaves

[Objective] This study aimed to uncover the biological characteristics of a parasitical fungus in Chrysosp/enium absconditicapsu/um J. T. Pan leaves. [Method] PDA medium was used to isolate the fungus from C. absconditicapsulum leaves; PDA medium, modified KB medium and Czapek medium were adopted to cultivate the isolated strain. [Result] Colonies of the strain were stretched, white, fedora- shaped with smooth and wavy edges, and showed diameter growth on PDA medi- um, modified KB medium and Czapek medium. At the late stage of culture, the colonies turned into cyanish brown on the above media. Spores were black and born on the surface of colonies on PDA medium with blackened medium. While on modified KB medium and Czapek medium, they were born at the edge of colonies with blackened medium. The spores varied in a wide range of shapes, mostly ob- clavate, sometimes spherical or ellipsoidal. The conidia were muriformly septate with transverse or longitudinal or oblique septations. The pseudo-beaks were short and cylindrical. [Conclusion] According to relevant literatures, the isolated strain is a fungus in Alternaria, Dematiaceae, Hylohomycetales, Hyphomycetes, Deuteromycotina.

Influence of different curing regimes on the microstructure and macro performance of UHPFRCC

This study investigates the influence of different curing regimes on the microstructure and macro properties of ultra-high performance fiber reinforced cementitious composite （UHPFRCC）, and aims to discover whether it is possible to produce qualified UHPFRCC using different curing regimes. A control mix of UHPFRCC is prepared. The mechanical performance and the short-term durability of the UHPFRCC matrix under three curing regimes are studied. In addition, the microstructures of the UHPFRCC matrix with different curing conditions are analyzed by combining scanning electron microscopy （SEM） and mercury intrusion porosimetry （MIP）. The results explore how different UHPFRCC curing regimes affect its microstructure and how the microstructure affects its macro behavior. Heat and steam curing for 3 d is succeeded to produce the UHPFRCC with nearly the same mechanical properties and durability as those of the 90 d standard curing. However, the heat cured UHPFRCC does not show great resistance to chloride-ion penetration.

In Vitro Propagation of Ardisia mamillata Hance

Ardisia mamillata Hance is a rare plant with highly ornamental and medicinal value. The traditional propagation methods for A. mamillata by seeds or cutting provided low proliferation rate. This study is to optimize the propagation technique of A. mamillata by tissue culture and set up an industrial production system to provide plenty of A. mamillata seedlings for the human demand. The optimal initiation medium for A. mamillata is MS +2.0 mg/L BA +0.1 mg/L NAA +30 g/L sugar, providing76.4% initiation rate. The optimal shoot proliferation medium for A. mamillata is MS+1.0 mg/L BA+0.1 mg/L NAA+30 g/L sugar, providing 4.56 fold proliferation rate and3.10 cm shoot in height. The optimal shoot elongation medium for A. mamillata is MS+0.5 mg/L BA+0.1 mg/L NAA+30 g/L sugar, providing 2.77 fold proliferation rate and 4.27 cm shoot in height. The optimal rooting medium for A. mamillata is 1/2MS+0.1 mg/L IBA +15 g/L sugar, providing 99.7% rooting rate, 4.0 roots per individual,7.53 cm root in length and 3.94 cm shoot in height. This provides a reliable mass propagation method for A. mamillata.

Potentiality of Vermicompost Humic Acids in Banana in Vitro Micropropagation Clone： Enano Guantanamero

The research was done at Havana Biofabric, Mayabeque Province. The vitro plants of banana （Musa sp） used came from the clone Enano Guantanamero （viand type）. They come from multiplication phase in a Murashige and MS （Skoog medium）. The objective of this work was to study the potentialities of HA （humic acids） for stimulation of rooting and cell division process, searching for completely synthetic hormone substitution due to its high cost. The multiplication medium contained thiamine （2 mg·L^-1）, myo-inositol （100 mg·L^-1）, sugar （30mg·L^-1）. By the use of HA, five treatments were used with total substitution of auxin and cytokinin （TI： HA （10 mg.Ll）; （T2： HA （20 mg·L^-1）; （T3： HA （30mg·L^-1）; （T4： HA （40 mg·L^-1）; （T5： HA （50 mg·L^-1） and the control with 6BAP （benzil amino purine） （4 mg·L^-1） ＋ IBA （indol butyric acid） （0.65 mg·L^-1）, pH of the medium was adjust just before agar were add. The results showed that in the explants under HA treatments, elongation and cell multiplication were favored confirmed by explants great high, root number and length due to dry mass. The total protein content, reduced carbohydrate and peroxidases enzymatic activity were determine. The use of Vermicompost HA in the in vitro micropropagation of banana allow the elimination of rooting phase saving materials and be able to pass explants directly to Acclimatization phase.

Rapid Propagation of Virus-free Sugarcane Plantlets via Temporary Immersion Bioreactor System

By employing temporary immersion bioreactor system(TIBs),we studied virus-free culture of seedlings from sugarcane varieties ROC16 and ROC22,from medium recipe,inoculation amount,sucrose concentration,and variety difference. The results showed,using this method,that proliferation rate of ROC16 improved by 40 times,per flask generated about 800 plantlets; of ROC22 improved by 30 times,per flask generated about 400-600 plantlets. The results provided basis for using TIBs in rapid propagation of plantlets via tissue culture.

The δ^15N response and nitrate assimilation of Orychophragmus violaceus and Brassica napus plantlets in vitro during the multiplication stage cultured under different nitrate concentrations

Natural nitrogen isotope composition(δ^(15)N) is an indicator of nitrogen sources and is useful in the investigation of nitrogen cycling in organisms and ecosystems. δ^(15)N is also used to study assimilation of inorganic nitrogen. However, the foliar δ^(15)N of intact plants, which is a consequence of nitrate assimilation occurring in the roots and shoots, is not suited for studying nitrate assimilation in cases where nitrate is the sole nitrogen source. In this study, Orychophragmus violaceus(Ov) and Brassica napus(Bn) plantlets, in which nitrate assimilation occurred in the leaves, were used to study the relationship between foliar δ^(15)N and nitrate assimilation.The plantlets were grown in vitro in culture media with different nitrate concentrations, and no root formation occurred for the plantlets during the multiplication stage.Nitrogen isotope fractionation occurred in both the Ov and the Bn plantlets under all treatments. Furthermore, the foliar nitrogen content of both the Ov and Bn plantlets increased with increasing nitrate concentration. Foliar nitrogen isotope fractionation was negatively correlated with foliar nitrogen content for both the Ov and Bn plantlets. Our results suggest that the foliar nitrogen isotope fractionation value could be employed to evaluate nitrate assimilation ability and leaf nitrate reductase activity.Moreover, high external nitrate concentrations couldcontribute to improved foliar nitrogen content and enhanced nitrate assimilation ability.

Transgenic Date Palm Containing Endotoxin Cry3Aa Gene

Date palm, like all other crops, is very sensitive to the injury by many insect pests, which may lead to the death of the affected plant and causes decrease in yield. In the present study, an efficient Agrobacterium for genetic transformation was successfully achieved for well known date palm （Phoenix dactylifera L.） cv. Medjool and Khalas using callus as explant. Embryogenic callus were recorded 100% mortality when cultured on MS medium containing 100 mg/L kanamycin with different cultivars, thus it was chosen for the selection of transformed explants. Embryogenic callus of Medjool and Khalas were incubated with Agrobacterium tumefaciens strain LBA 4404 for 0.5, 1, 2, 4 and 24 h on LB medium. After the incubation periods, embryogenic callus was transferred to MS medium with 0.1 mg/L NAA, 0.05 mg/L BA, 250 mg/L carbenicillin and 100 mg/L kanamycin for detection of transgenic embryogenic callus. Polymerase chain reaction （PCR） was used for the rapid screening of Cry3Aa gene. For screening, total genomic DNA was isolated from transformants. Using primer specific to Cry3Aa gene （forward and reverse）, a PCR product with a size of about 2,000 bp was amplified when all nucleic acid from the transformants were utilized as templates. PCR analysis confirmed the appearance of the transgene of 2,000 bp in one individual plantlet. Presence and integration of foreign Cry3Aa gene in regenerated kanamycin resistant embryogenic callus was also confirmed by Southern blot hybridization. It was found that one transgenic embryogenic callus for both Medjool and Khalas showed a single copy of gene integration. These results signify the successful transfer of Cry3Aa gene into date palm plant.