查询词典 oxalis

Investigated the antimicrobial effect of Oxalis corniculata L..

研究酢浆草乙醇提取物的抑菌活性。

The results showed that the species of Oxalis could be classified on the basis of the shape, the size and exine sculpture of pollen grains.

结果表明：该属花粉粒大小、形状和外壁雕纹可作为分种的依据。

Results showed that 0.01g/mL extract of Oxalis corniculata L. had obvious antimicrobial effect on S. aureus, but all extract of Oxalis corniculata L has not any antimicrobial effect on E.

结果表明，0.01g/ml的提取物对摇床培养的金黄色葡萄球菌生长具有明显的抑制作用；但各种浓度的提取物对摇床培养的大肠杆菌生长均无抑制作用。

Oxalis corymbosa to outside species as experimental material Oxalis corymbosa pot study alien species under drought stress in different enzyme superoxide dismutase and peroxidase activity of the physiological indices.

以外来物种铜锤草为实验材料，通过盆栽研究外来物种铜锤草在不同的干旱胁迫下超氧化物酶和过氧化物酶酶活性的生理指标变化。

To improve the efficiency of Oxalis triangularis purpurea breeding, this study is done by leaf explant. 0.5 mg/L 6-BA and 0.5 mg/L NAA are added to the culture based on the last study. KT and 2,4-D concentrations impact on Oxalis triangularis purpurea regeneration system by "one-step method" are further studied.

为提高三角紫叶酢浆草的育苗效率，以三角紫叶酢浆草叶片为材料，在现有研究的基础上，采用固定配比的6-BA(0.5mg/L)和NAA(0.5mg/L)，研究了KT、2，4-D对"一步法"诱导三角紫叶酢浆草再生体系的影响。

One-step method induced Oxalis triangularis purpurea regeneration system may reduce the workload effectively, moreover, with a characteristic of high efficiency induced regeneration seedlings, which is propitious to Oxalis triangularis purpurea breeding.

一步法诱导形成三角紫叶酢浆草再生体系方法能有效的降低工作量，而且具有再生苗诱导效率高的特点，有利于规模化繁育三角紫叶酢浆草。

The risk of alien invasive plant--Oxalis Corymbosa was studied with referring to the pest risk analysis method and the amended adjudge criterion of this paper ,The result indicate that Oxalis Corymbosa is a more devastating alien invasive plant, The paper suggest the related management department shoud make some measures to resolve this problem in time.

借鉴有害生物危险性分析方法和运用本文修改的判断指标内涵研究了南岳自然保护区外来入侵植物红花酢浆草的危险性，结果表明红花酢浆草处于高度危险性等级，建议管理部门尽快采取合理的防治措施及时予以解决。

Producing PHAs,and then were orientationally inserted into a prokaryotic expression vector pBV220. By analyzing the bioactibity and function of their products, the biological function of phaA, phaB and phaC was confirmed. These have been done in our laboratory. To make better use of the three genes by plant bioreactor, two groups of different plant expression vectors that can be used to produce PHAs in different plants were constructed, and the transformation of PHA in Oxalis triangnlaris has been preliminarily reseached.The following is the main results:Three plant expression vectors pBI121-A,pBI121-B and ubquiting-C, which can be used to be transformed into Oxalis triangularis were respectively constructed by using the phaA, phaB and phaC.

菌株的亚克隆基因组片段中，分离出phaA、phaB和phaC三个基因片段，定向克隆至原核表达载体pBV220，通过对其生物活性与功能分析，确证了基因phaA、phaB和phaC的生物学功能；为了通过植物生物反应器对这三个基因进一步研究利用，本实验利用这三个基因构建了两组可用于不同植物生产PHA的真核表达载体，并对紫叶酢浆草进行PHA基因遗传转化的初步研究，获得主要结果如下：利用克隆的phaA、phaB、phaC三个基因分别构建了可用于转化紫叶酢浆草表达载体pBI121-A、pBI121-B、uBquiting-C；可用于玉米转化的种子特异性表达载体p7S-A、pBI121-S-B、uBquiting-C。

By reseaching the tissue culture of Oxalis trisngularis, regeneration system of Oxalis trisngularis was preliminaryly established and the optimum mediums were MS+2,4-D 1.5mg/L+6-BA 0.1 mg/L for inducing callus and MS+NAA 0.9 mg/L +6-BA 0.4 mg/L for inducing differentiation, and MS+2,4-D 0.5mg/L for inducing rooting.

筛选出诱导愈伤的最佳培养基为MS+2，4-D 1.5mg/L+6-BA 0.1 mg/L；分化的最佳培养基为MS+NAA 0.9 mg/L +6-BA 0.4 mg/L；生根培养基为MS+2，4-D 0.5 mg/L；愈伤组织Kan抗性筛选的最佳浓度为58 mg/L。

To improve the efficiency of Oxalis triangularis purpurea breeding, this study is done by leaf explant. 0.5 mg/L 6-BA and 0.5 mg/L NAA are added to the culture based on the last study. KT and 2,4-D concentrations impact on Oxalis triangularis purpurea regeneration system by "one-step method" are further studied.

为提高三角紫叶酢浆草的育苗效率，以三角紫叶酢浆草叶片为材料，在现有研究的基础上，采用固定配比的6-BA(0.5mg/L)和NAA(0.5mg/L)，研究了KT、2，4-D对&一步法&诱导三角紫叶酢浆草再生体系的影响。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。