两种螺旋藻在不同生长阶段的硒胁迫和生物有机化效应

在极大螺旋藻(S.maxima)和钝顶螺旋藻(S.platensis)不同生长阶段进行硒胁迫处理,分别从接种后第1d至第5d开始添加硒,并不断增加硒含量,至第7d使硒的累计添加量为1000mg·L^-1,形成5种不同硒胁迫(硒胁迫Ⅰ～Ⅴ),观察各种硒胁迫下螺旋藻的生物量及对无机硒的生物有机化的影响。结果表明:硒胁迫Ⅰ～Ⅳ对两种螺旋藻的生长影响不明显,而硒胁迫Ⅴ对螺旋藻生长有明显促进作用;藻体含硒总量和螺旋藻对无机硒的有机化率按硒胁迫Ⅰ～Ⅴ依次增加。首次提出硒胁迫强度概念,并用此较好地解释了有关实验结果。     

氨基酸叶面硒肥对铁皮石斛富硒及多糖含量的影响

研究不同浓度氨基酸叶面硒肥(CK、1200倍液、900倍液和600倍液)对智能温室人工栽培红杆铁皮石斛(Dendrobium officinale)枝条(即鲜条)富硒、抽芽和多糖含量的影响。结果表明,氨基酸硒肥各浓度处理均极显著提高鲜条硒和多糖含量。鲜条硒含量与氨基酸硒肥浓度呈正相关,且各处理间达极显著差异。鲜条多糖含量在氨基酸硒肥浓度较低(CK、1200、900倍液)时呈正相关,并在氨基酸硒肥900倍液时达最高(35.213 g·kg-1),之后呈递减趋势。氨基酸硒肥稀释达900倍时,90%以上鲜条已抽出3片韧叶,表明氨基酸硒肥明显促进鲜条生长。因此,环保型氨基酸硒肥900倍液是铁皮石斛营养积累前期较适宜浓度。     

钝顶螺旋藻富集转化硒及硒在藻体中的分布

钝顶螺旋藻在４℃、避光、隔离空气条件下,对硒的吸附量死体显著高于活体。藻体对硒的最大富集量为６２７．４μg.g^-1(DW),培养基中硒浓度在３００μg.ml^-1以下时有机硒转化率大于８０％。藻体中的硒主要分布在水溶性组化率大于８０％。藻体中的硒主要分布在水溶性组分中,占总硒的６５％以上,蛋白质硒占有机硒的７１．９％,多糖、核酸也有一定量硒分布。     

富硒灵芝菌丝多糖、蛋白的提取及其体外抗氧化和抗肿瘤活性研究

灵芝具有较强的硒富集能力，其中的硒元素多以硒多糖、硒蛋白等有机硒形式存在。本研究以灵芝菌丝为研究对象，采用不同方法提取菌丝多糖及菌丝蛋白，探究外源施硒对二者的含量及其抗氧化活性的影响，并初步探究了水提多糖和可溶性蛋白的抗肿瘤活性。结果表明，以硒含量为95μg/mL的培养基发酵得到的菌丝体，其可溶性蛋白及硒含量较高，分别为1.630 8 mg/g和36.905 7μg/g;采用超声辅助碱提法时，多糖含量较高，为32.070 9 mg/g,且该多糖的硒含量为33.864μg/g。与对照组相比，富硒组灵芝菌丝体其多糖和蛋白的抗氧化性较强，且均表现出浓度依赖性。此外，富硒灵芝菌丝体其硒多糖对肿瘤细胞的抑制增殖效果较好，对HCCLM、A549和HSC-3肿瘤细胞的IC₅₀值分别为3.765、3.23和2.267 mg/mL;但其硒蛋白对上述三种癌细胞的增殖抑制效果较差，其IC₅₀值分别为636.987、506.97、555.598μg/mL。     

木耳硒多糖的分离纯化及对腹水型S_(180)细胞膜流动性的影响

应用DEAE52-cellulose、SephacrylS-500HR柱层析从自培养的富硒木耳中分离纯化得到4种木耳硒多糖,SeAPⅠ-1、SeAPⅠ-2、SeAPⅡ和SeAPⅢ,紫外扫描显示在280nm和260nm均无吸收,表明不含蛋白质和氨基酸;高效凝胶渗透色谱为单一对称峰,表明4种硒多糖均为均一多糖。对S180细胞膜的游离脂肪酸和膜脂流动性的研究显示,4种硒多糖具有较好的活性,且SeAPⅠ-2、SeAPⅡ的活性显著强于SeAPⅠ-1、SeAPⅢ(p0.05)。     

秦巴山区富硒蛹虫草有效成分及硒存在形态分析

为探究秦巴山区富硒蛹虫草有效成分及硒存在形态,以秦巴山区蛹虫草CM-1518为研究对象,研究不同质量分数亚硒酸钠(0～500 mg/kg)对蛹虫草生长发育的影响,并对其有效成分及硒存在形态进行分析。试验结果表明当亚硒酸钠质量分数为100 mg/kg时,蛹虫草鲜质量最高,为293.41 g/盒。当亚硒酸钠质量分数为200 mg/kg时,虫草素、虫草酸含量最高,分别为1.06 mg/g和2.10 mg/g,表明硒与虫草素和虫草酸可协同增效,但虫草多糖含量变化规律不明显,亚硒酸钠的添加不利于腺苷的合成积累。经计算,富硒蛹虫草中有机硒所占百分比均高达99.9%,低浓度的亚硒酸钠可促进可溶性蛋白和可溶性多糖中硒的合成,但高浓度的硒却降低其合成,且富硒蛹虫草中可溶性多糖中硒含量高于可溶性蛋白硒含量。试验表明适宜浓度的亚硒酸钠可促进蛹虫草生长发育及有效成分合成积累。     

硒对猪细小病毒体外增殖抑制作用的研究

本文以PK-15细胞为模型,研究了亚硒酸钠、硒蛋氨酸和海藻硒多糖等三种硒化合物对猪细小病毒体外复制 的抑制作用,以及还原型谷胱甘肽、D-甘露醇等氧自由基清除剂对不同来源硒的抑制病毒作用的影响。结果表明: 三种硒化合物对猪细小病毒在PK-15中的复制呈现不同程度的抑制作用,在相同浓度时其强度依次为硒蛋氨酸、 亚硒酸钠、海藻硒多糖,随着浓度的增加,其抑制作用逐渐增强,呈剂量依赖性关系。还原型谷胱甘肽和甘露醇均 有增强硒的抑制病毒复制作用,两者同时添加时,协同增强硒的抑制病毒复制作用。     

硒对猪细小病毒体外增殖抑制作用的研究

本文以PK-15细胞为模型,研究了亚硒酸钠、硒蛋氨酸和海藻硒多糖等三种硒化合物对猪细小病毒体外复制的抑制作用,以及还原型谷胱甘肽、D-甘露醇等氧自由基清除剂对不同来源硒的抑制病毒作用的影响.结果表明三种硒化合物对猪细小病毒在PK-15中的复制呈现不同程度的抑制作用,在相同浓度时其强度依次为硒蛋氨酸、亚硒酸钠、海藻硒多糖,随着浓度的增加,其抑制作用逐渐增强,呈剂量依赖性关系.还原型谷胱甘肽和甘露醇均有增强硒的抑制病毒复制作用,两者同时添加时,协同增强硒的抑制病毒复制作用.     

富硒食用菌多糖的体外抗氧化研究

分别采用还原力、羟自由基、超氧阴离子自由基、[DPPH.]体系和卵磷脂脂质过氧化体系等几种不同的体外抗氧化模型,对超声波法提取得到的富硒食用菌多糖的抗氧化能力进行了研究。结果表明,在各种体系中,富硒食用菌多糖均表现出较高的抗氧化性,且其浓度与抗氧化活性呈一定的量效关系,在相同的多糖浓度下,体系的抗氧化活性与硒含量有关。     

土壤含硒量极高极低地区黄豆中硒的含量及其在不同组分中的分布

分别从湖北省的恩施（高硒）、北京（中硒）、吉林省的延边和甘肃省的天水（低硒）采集黄豆样品,用两套独立的连续化学提取法提取低分子量化合物、脂类、核酸、蛋白及多糖等组分并测定其硒含量,研究了黄豆不同结合态硒含量的分布规律。结果表明：土壤中硒含量高低悬殊地区黄豆的硒含量相应高低不等,但其中硒在不同结合态中的分布没有系统差异。蛋白结合的硒量占黄豆硒总量的５０％～６６％以上,其中水溶蛋白结合硒量达４２．６％～５６．７％,为优势硒结合形态。同时发现丙酮溶解的脂肪部分不含硒,但脂蛋白、核酸和多糖组分含有硒。样品的蛋白质和氨基酸含量分析结果还表明恩施高硒地区黄豆中的蛋白质和氨基酸含量相对较高。     

CMV promotor activity during ES cell differentiation: potential insight into embryonic stem cell differentiation

The activity of the P(CMV IE) promoter was studied during the differentiation of ES cells into neurons. In order to do this, stable embryonic stem (ES) cell lines that express enhanced green fluorescent protein (EGFP) under the control of P(CMV IE) were created and these ES cells were differentiated by aggregation of cells in the presence of retinoic acid (RA). Based on our observations that the activity of P(CMV IE) was highest in undifferentiated cells, and that cell-cell interaction and addition of RA that lead to enhanced cell proliferation also increased expression from P(CMV IE), we hypothesized that the activity of P(CMV IE) was positively regulated in cycling cells. However, when analysis was done at the single cell level it was found that BrdU label and EGFP expression were not correlated. EGFP expression was found to be down-regulated in many cells that were BrdU positive and conversely there were significant numbers of BrdU negative cells that were EGFP positive. Further, P(CMV IE) activity was not observed in cells that were nestin positive or in differentiated neurons, but P(CMV IE) was active in cells with a fibroblast-like morphology. Finally, several proteins present in undifferentiated ES cells were found to bind to regulatory regions of P(CMV IE). These were absent when cells were aggregated in the presence of RA. The above results have implications for expression of transgenes in ES cells as well as providing new insight into the mechanism of lineage restriction.     

Toxicity and Mutagenesis of Chrysotile Asbestos toAgrobacterium radiobacter

The mutation of Agrobacterium radiobacter cells exposed to chrysotile asbestos was examined by the random amplified polymorphic DNA (RAPD) method. Approximately 1.4 kbp of DNA in A. radiobacter, which was not amplified strongly in the cells that were not exposed to asbestos, was amplified in the cells that were exposed to asbestos. Mutation in genomic DNA of A. radiobacter was found to be induced by asbestos. Specific DNA that was amplified by asbestos present in PCR products and that which exists latently in genomic DNA were cloned, and these sequences were then determined and compared. It was shown that one of the mutations by the asbestos in the A. radiobacter occurred only in the primer annealed region and was a point mutation or deletion.     

长期水分胁迫对小麦生育中后期根叶渗透调节能力、渗透调节物质的影响

以 2个抗旱性强的和 2个抗旱性弱的小麦品种为材料 ,研究了中度及严重水分胁迫对根系及叶片渗透调节能力的影响。结果表明 :随着水分胁迫的加剧 ,叶片的渗透调节能力增强 ,但在籽粒迅速扩大的灌浆期 ,叶片的渗透调节能力下降。去穗处理明显地提高叶片的渗透调节能力。说明叶片渗透调节能力的高低与同化物的供应及分配有关。不同品种根系渗透调节能力与叶片基本一致 ,但根系的渗透调节能力低于叶片。开花、灌浆期根系的渗透调节能力大大降低 ,严重水分胁迫下根系的渗透调节能力低于中度水分胁迫。这一方面与同化物的供应有关 ,另一方面严重水分胁迫还会对根细胞造成损伤 ,对根系的渗透调节能力产生影响。渗透调节物质的变化趋势与渗透调节能力基本一致。叶片中 K+对渗透调节的贡献最大 ;其次是可溶性糖 ,6种渗透调节物质排列顺序为 K+>可溶性糖 >游离氨基酸 >Ca2 +>Mg2 +>Pro。根系中仍以 K+占绝大部分 ,但根系中 Ca2 +也是不可忽视的成分之一。     

Spatial distribution and mortality process ofAnoplophora malasiaca (Coleoptera: Cerambycidae) eggs in citrus groves

The study was carried out in two (A and B) citrus groves to clarify the spatial distribution patterns of eggs and larvae, and to analyse the mortality process of eggs. From the analysis by using the mean density and the mean crowding, it was clarified that the distributions of eggs were contagious and that larvae were more contagiously distributed than eggs. The τ and z indices showed that the operation of egg mortality was inversely density-dependent in both groves, and that the degree of inverse density-dependence was greater in A than in B grove. The spatial correlations between the emergence holes and the eggs or larvae in each tree, which were analysed by using ω index, showed that the distributions were more overlapping between the emergence holes and the larvae than the eggs. As the result of dividing trees into several groups according to the number of emergence holes, it was clarified that the survival rates of eggs were positively correlated with the number of emergence holes. In conclusion, inversely density-dependent mortality process was considered to be caused by lower mortality rates of eggs in the trees with more emergence holes. Especially in A grove, because the trees with more emergence holes were larger in diameter and more egg oviposition, the inversely density-dependent mortality process was considered to be detected more conspicuously than in B grove.     

Production of ROL gene transformed plants of Rosa hybrida L. and characterization of their rooting ability

Transgenic plants of the rootstock Rosa hybrida L. cv. Moneyway were produced via a two-step procedure. First, kanamycin-resistant roots were generated on stem slices from micropropagated shoots, which were cocultivated with Agrobacterium tumefaciens containing the neomycin phosphotransferase II (NPTII) gene for conferring kanamycin resistance, together with individual ROL genes from A. rhizogenes. Root formation was quite efficient and up to two kanamycin-resistant roots per stem slice were produced. In the second step, these roots were used to regenerate transgenic plants via somatic embryogenesis. Although regeneration lasted up to 12 months, production of several transformants was successfully accomplished. Untransformed escapes were not found, indicating that the initial selection on kanamycin resistance was reliable.The presence of a combination of ROLA, B and C genes enhanced adventitious root formation on micropropagated shoots and explants of stems and leaves. It appears that the auxin sensitivity was increased to such a degree that cells were able to respond even to endogenous auxins present in shoots and leaves. Rooting experiments in greenhouse demonstrated that adventitious root formation on cuttings was improved threefold upon introduction of these ROL genes. It is concluded that a method was developed for the production of ROL gene transformed roses with improved rooting characteristics.     

一种新型粘多糖结构与性能的检测

粘多糖是由糖醛酸和氨基己糖交替连接成的高分子物质, 理化性质独特, 应用范围广泛。通过对突变株兽疫链球菌Streptococcus zooepidemicus BU100进行发酵, 可产一种新型粘多糖(下文用粘多糖A代替)。利用咔唑法、Elson-Morgan法、考马斯亮蓝法、红外光谱以及13C核磁共振谱测定粘多糖A的结构, 结果显示粘多糖A中糖醛酸和氨基糖的摩尔比例接近1:1, 蛋白含量符合标准(<0.1%); 粘多糖A图谱中出现的结构特征峰大部分与透明质酸相同。对粘多糖A的实用性能进行检测, 并用透明质酸做对比, 结果表明透明质酸在两种湿度下的吸湿性均要好于粘多糖A, 但粘多糖A的保湿性要好于透明质酸。粘多糖A总体的抗氧化性好于透明质酸, 并且粘多糖A耐透明质酸酶。粘多糖A可作为保湿剂、润滑剂、抗氧化剂等被更加有效地应用在医疗和化妆品等领域。     

医院工作人员鼻腔葡萄球菌带菌状况年度推移的调查报告

本文报道1989年从202名医院工作人员鼻腔分离葡萄球菌的带菌状况和药敏性检测结果。并将此结果同作者等于1985年对200名同类人员检测的结果相比较,作了年度推移的调查分析发现1989年度的总带菌率(76.6％)比1985年度(84.5％)略有下降,但其中的金黄色葡萄球菌带菌率却从1985年的7.5％上升为10.4％。从1989年和1985两个年度的调查中,均发现临床科室人员金葡菌带菌率高于其它辅助科室人员,说明医务人员带菌率与接触病人成正相关关系。分离菌株对12种抗菌药物的耐药性检测结果显示,1989年分离菌株对其中9种的敏感性下降,并且从耐药谱显示出对5种抗菌药物耐药的多重耐药菌株明显增多。另从金葡菌的耐药情况,也看出1989年的耐药率高于1985年菌株。还在1989年分离的金葡菌中出现25％的耐甲氧西林菌株。     

Comparison of genetic diversity at microsatellite loci in near-extinct and non-endangered species of Mexican goodeine fishes and prediction of cross-amplification within the family

The cross-utility of 12 microsatellite loci (including nine newly developed loci) amongst the viviparous subfamily, the Mexican Goodeinae, was assessed, examining both the probability of amplification and the potential incidence of null alleles from tests of F _IS. Genetic diversity was relatively high in comparison to other freshwater species. Amplification success was not correlated with genetic distance between microsatellite source and target species, but taxa that were more distantly related were less likely to be cross-polymorphic for microsatellite loci. On average, species that were cross-polymorphic were separated by a genetic distance of 15% at the cytochrome oxidase I locus, while those that were monomorphic were separated by 19%. There was no evidence that null alleles become more frequent at greater source-target genetic distance.     

Iron uptake byBifidobacterium thermophilum protoplasts

Protoplasts ofBifidobacterium thermophilum were prepared by a combination of lysozyme and protease digestion, and ferrous iron uptake studies were carried out. Little, if any, iron was internalized by the protoplasts, although large amounts of iron were bound to the protoplast surface. This binding was much greater than that of intact cells, which prefer to internalize iron by an energy-dependent process. It was also found that the binding of iron by protoplasts of cells grown in an iron-deficient medium was much more extensive than that of cells grown in an iron-sufficient medium. Soluble and particulate fractions of protoplasts were prepared by grinding them in a glass homogenizer, and the particulate fraction was also subjected to iron binding studies. The amount of iron bound was the same as that in intact protoplasts, indicating that the particulate fraction membrane fragments bound iron on their outer surface only. Nevertheless, when iron-preloaded cells were protoplasted and their surface cleared of iron, their particulate fraction contained considerable amounts of iron, indicating that the inner surface of the membranes is capable of binding iron as long as the cell is intact. The amount of iron so bound was dose-dependent on the amount of iron entering the cell. The failure of the outer and inner surface iron pools to mix was confirmed by the fact that when iron-preloaded protoplasts were incubated with additional iron, only the latter (surface-bound) was elutable with nonradioactive 2 mM FeSO₄. It is concluded that increasing bifidobacterial iron load increases the amount of iron bound to the inner surface of the membrane; the procedure, which is effective in forming bifidobacterial protoplasts, destroys their iron transport mechanism while uncovering surface iron-binding sites; and that such iron-binding sites may be of significance in the cellular iron metabolism processes.