羚牛(Budorcas taxicolor)部分脏器特点的观察

本文对2只羚牛的雌性生殖器官及肝、肾、脾等脏器进行了形态描述,并与黄牛及羊的相应器官进行了比较,为探讨羚牛的分类地位提供了解剖学资料。     

Carbohydrate metabolism in Musa paradisiaca

Considerable variations exist in the content of glucose, fructose, sucrose, starch and protein and in the activities of enzymes involved in carbohydrate metabolism between different parts of the banana plant (Musa paradisiaca). Sucrose synthetase is present in the highest concentration in rootstock and fruit pulp, and sucrose phosphate synthetase in the pseudostem. The highest ratio of the activity of sucrose phosphate synthetase to sucrose synthetase is found in leaves. Acid invertase is present in leaves, leaf-sheath and fruit pulp and is not demonstrable in rootstock and pseudostem. Neutral invertase activity is high in pseudostem and leaf-sheath. Starch phosphorylase is largely concentrated in fruit pulp and rootstock. The maximum activity of ATP:d-phosphoglucose (ADPG) pyrophosphorylase is found in rootstock. β-Amylase is not demonstrable in rootstock and is largely concentrated in leaf-sheath. Hexokinase is most active in rootstock and the lowest in leaves. Acid phosphatase and alkaline phosphatase activity is highest in fruit pulp and pseudostem. Glucosephosphate isomerase is most active in the rootstock and lowest in the leaves.     

Using immunohistochemistry to study plant metabolism: the examples of its use in the localization of amino acids in plant tissues, and of phosphoenolpyruvate carboxykinase and its possible role in pH regulation

To understand many aspects of the metabolism of complex plant structures such as leaves, fruit and roots it is important to understand how metabolic processes are compartmentalized between tissues. The aim of this article is to show how immunohistochemistry, in conjunction with biochemical and physiological studies, is useful in understanding both the function of an enzyme in a tissue and metabolic processes occurring in plant tissues. This is illustrated by two examples. Firstly, the use of immunohistochemisty in the localization of amino acids in plant tissues is described. Secondly, the use of immunohistochemistry in understanding the function of an enzyme in a tissue and the metabolic processes occurring within the tissue is described. To illustrate this the example of phosophoenolpyruvate carboxykinase (PEPCK), an enzyme which is present in many plant tissues in which its function is unknown, is used. Evidence is provided that PEPCK may play a role in pH regulation in tissues active in the metabolism of nitrogen.     

松嫩草原不同时间火烧后植物个体特征变化分析

松嫩草原不同时间火烧后,羊原高度不同程度的降低,尤以晚烧地最低但羊草个体重量这间无显著差异,产量的差异主要来自密度影响,火烧后,羊草叶片数增多、增宽,早烧地增长,晚烧地缩短,芦苇和寸草苔高生长也受火烧影响,但寸草苔高度后期差异消失。     

新疆天然与种植黑加仑果实的营养成分分析与比较

本文通过新疆种植黑加仑和天然黑加仑的脂肪油、八种微量元素、十七种氨基酸以及维生素C的含量进行测定比较,得出：天然黑加仑脂肪油含量为17.9%,种植黑加仑脂肪油含量为12.9%,其中,天然黑加仑脂肪油中,r－亚麻酸的含量为19.02%,而种植黑加仑中,其含量为10.20%,天然黑加仑中K,Na,Ca,Cu,Zn的含量比种植黑加仑含量高,但同时Fe,Mn,Mg元素的含量却比种植黑加仑含量低。种植黑加仑的维生素C含量为99.6mg/g,天然黑加仑的含量为108mg/g,天然黑加仑的氨基酸的总量为1.63%,种植黑加仑为1.55%。     

DNA polymerase I-mediated ultraviolet repair synthesis in toluene-treated Escherichia coli.

DNA synthesis after ultraviolet irradiation is low in wild type toluene-treated cells. The level of repair incorporation is greater in strains deficient in DNA polymerase I. The low level of repair synthesis is attributable to the concerted action of DNA polymerase I and polynucleotide ligase. Repair synthesis is stimulated by blocking ligase activity with the addition of nicotinamide mononucleotide (NMN) or the use of a ligase temperature-sensitive mutant. NMN stimulation is specific for DNA polymerase I-mediated repair synthesis, as it is absent in isogenic strains deficient in the polymerase function or the 5' leads to 3' exonuclease function associated with DNA polymerase I. DNA synthesis that is stimulated by NMN is proportional to the ultraviolet exposure at low doses, nonconservative in nature, and is dependent on the uvrA gene product but is independent of the recA gene product. These criteria place this synthesis in the excision repair pathway. The NMN-stimulated repair synthesis requires ATP and is N-ethylmaleimide-resistant. The use of NMN provides a direct means for evaluating the involvement of DNA polymerase I in excision repair.     

红腹锦鸡血细胞的光镜和扫描电镜观察

为了探讨红腹锦鸡(Chrysolophus pictus)血细胞的形态特征,为生理学研究提供生物学基础资料,利用光镜和扫描电镜观察了红腹锦鸡血细胞的形态特征。结果表明,红腹锦鸡红细胞呈椭圆形或扁圆形,表面光滑,具核;白细胞为球形,体大,淋巴细胞表面有绒毛状突起,嗜中性粒细胞核一般分2~5叶,嗜酸性粒细胞核一般分2叶,嗜碱性粒细胞核分2~3叶,单核细胞表面粗糙不平,核大,呈肾形或圆形;凝血细胞呈球形或不规则形。     

Iron uptake by Chang cells from transferrin,nitriloacetate and citrate complexes: The effects of iron-loading and chelation with desferrioxamine

Iron uptake by Chang liver cells in culture is about thirty times as great when ferric nitriloacetate is used as a donor as when iron-transferrin is used. Iron uptake from ferric citrate is no greater than from iron-transferrin. Most of the intracellular iron derived from transferrin is found in the supernatant after 20 000 × g centrifugation of the cell homogenate for 40 min: about half of this is in the form of ferritin. Iron derived from ferric nitriloacetate is found largley in the membranous pellet after centrifugation and very little of this is in the form of ferritin.Iron incorporated in cytosol ferritin is easily available for chelation by desferrioxamine and this process is facilitated by ascorbic acid. Membrane-bound iron is less available for chelation. This tissue culture model forms a convenient basis for the study of iron overlead and iron chelation.     

Xanthine oxidoreductase is present in bile ducts of normal and cirrhotic liver

Xanthine oxidoreductase (XOR) is a widely distributed enzyme, involved in the metabolism of purines, which generates superoxide and is thought to be involved in free radical-generated tissue injury. It is present at high concentrations in the liver, from where it may be released during liver injury into the circulation, binding to vascular endothelium and causing vascular dysfunction. The cellular localization of the enzyme, essential to understanding its function, is, however, still debated. The present study has used a highly specific mouse monoclonal antibody to define the cellular distribution of XOR in normal and cirrhotic human liver. As shown previously, XOR is present in hepatocytes. However, the novel finding of this study is that XOR is present in bile duct epithelial cells, where it is concentrated toward the luminal surface. Moreover, in liver disease, proliferating bile ducts are also strongly positive for XOR. These findings suggest that the enzyme is secreted into bile, and this was confirmed by analysis of human and rat bile. Xanthine oxidase activity was 10 to 20-fold higher in liver tissue obtained from patients with liver disease, than in healthy liver. We conclude that XOR is expressed primarily in hepatocytes, but is also present in bile duct epithelial cells and is secreted into bile. Its role in bile is unknown but it may be involved in innate immunity of the bowel muscosa.     

Cytoplasmic localization of the ORF2 protein of hepatitis E virus is dependent on its ability to undergo retrotranslocation from the endoplasmic reticulum

Hepatitis E virus (HEV) is a positive-strand RNA virus that is prevalent in much of the developing world. ORF2 is the major capsid protein of HEV. Although ORF2 is an N-linked glycoprotein, it is abundantly located in the cytoplasm in addition to having membrane and surface localization. The mechanism by which ORF2 protein obtains access to the cytoplasm is unknown. In this report, we prove that initially all ORF2 protein is present in the endoplasmic reticulum and a fraction of it becomes retrotranslocated to the cytoplasm. The ability of ORF2 to be retrotranslocated is dependent on its glycosylation status and follows the canonical dislocation pathway. However, in contrast to general substrates of the dislocation pathway, retrotranslocated ORF2 protein is not a substrate of the 26S proteasome complex and is readily detectable in the cytoplasm in the absence of any protease inhibitor, suggesting that the retrotranslocated protein is stable in the cytoplasm. This study thus defines the pathway by which ORF2 obtains access to the cytoplasm.     

Proteolipid protein 2 mRNA is expressed in the rabbit embryo during gastrulation

The expression pattern of the receptor tyrosine kinase gene EphB3 was examined during the early stages of chick embryogenesis, and is described in this report. In the gastrula, EphB3 is expressed in epiblast cells adjacent to and entering the anterior portion of the primitive streak; expression is extinguished once cells have ingressed. At headfold stages, EphB3 is strongly transcribed in the floor of the foregut and in anterior lateral endoderm, and is expressed in the subjacent cardiogenic mesoderm. EphB3 is transiently expressed in the lateral ectoderm, neural tube, and neural crest during these stages. Later neural expression is localized to the mesencephalon. In the somitic mesoderm, EphB3 is initially expressed in the sclerotome, but later is expressed predominantly in the dermatome. Prominent expression is also detected in the developing heart, liver, posterior ventral limb bud mesenchyme, pharyngeal arches, and head mesenchyme.     

Translational-entropy gain of solvent upon protein folding

We show that even in the complete absence of potential energies among the atoms in a protein-aqueous solution system, there is a physical factor that favors the folded state of the protein. It is a gain in the translational entropy (TE) of water originating from the translational movement of water molecules. An elaborate statistical-mechanical theory is employed to analyze the TE of water in which a protein or peptide with a prescribed conformation is immersed. It is shown that if the number of residues is sufficiently large, the TE gain is powerful enough to compete with the conformational-entropy loss upon folding. For protein G we have tested over 100 compact conformations generated by a computer simulation with the all-atom potentials as well as the native structure. A significant finding is that the largest TE is attained in the native structure. The translational movement of water molecules is quite effective in achieving the tight packing in the interior of a natural protein. These results are true only when the solvent is water whose molecular size is the smallest among the ordinary liquids in nature.     

Fixation probability in spatially changing environments.

The fixation probability of a mutant in a subdivided population with spatially varying environments is investigated using a finite island model. This probability is different from that in a panmictic population if selection is intermediate to strong and migration is weak. An approximation is used to compute the fixation probability when migration among subpopulations is very weak. By numerically solving the two-dimensional partial differential equation for the fixation probability in the two subpopulation case, the approximation was shown to give fairly accurate values. With this approximation, we show in the case of two subpopulations that the fixation probability in subdivided populations is greater than that in panmictic populations mostly. The increase is most pronounced when the mutant is selected for in one subpopulation and is selected against in the other subpopulation. Also it is shown that when there are two types of environments, further subdivision of subpopulations does not cause much change of the fixation probability in the no dominance case unless the product of the selection coefficient and the local population size is less than one. With dominance, the effect of subdivision becomes more complex.     

鼎湖山顶级森林生态系统水文要素时空规律

运用连续7a(1993～1999)的水文观测资料,对南亚热带顶级生态系统鼎湖山季风常绿阔叶林集水区水文要素时空规律进行分析,得到如下一些主要结论：(1)鼎湖山多年平均降水量为1910mm,湿季降水量占年降水量80％,干季仅占20％。6月份的降水量最大,1月份最小。(2)季风常绿阔叶林冠层截留率为31．8％,湿季的截留量占全年截留量的66．7％,截留量最大值和最小值所在的月份分别为7和1月份。各月的截留率差异很大,截留量大的月份,截留率较低;截留量小的月份,截留率较高。(3)季风常绿阔叶林集水区多年平均总径流量953．0mm,总径流系数49．9％,其中地表径流量为252．3mm,地表径流系数13．2％;地表径流与降水量之间存在二次抛物线型回归关系,与降水强度的关系不大,这说明季风常绿阔叶林的产流形式是是蓄满产流。(4)季风常绿阔叶林多年平均蒸散948．2mm,占同期降水量的49．7％;蒸散力1031．4mm,年蒸散系数为0．92,蒸散月变化规律较降水量的月变化规律有所滞后。(5)系统贮水量的月变化很大,2～8月份,系统处于蓄水阶段;9月份至翌年1月份,系统处于失水阶段。蓄水和失水的最大值分别出现在湿季和干季的第一个月,即4月份和10月份。(6)集水区多年平均水量总输入2129．9mm,实际输入1910mm(降水量),其中219．9mm的水量输入是由系统贮水量变化而产生。支出的总水量2129．9mm,实际支出1901．3mm(径流和蒸散量),其中228．6mm的水量支出是由系统贮水量变化引起的。     

Beta-Galactosidase messenger RNA made during recovery from inhibition of protein synthesis is not translated.

Bacteria that accumulate RNA in the course of inhibition of protein synthesis are impaired in their ability to synthesize beta-galactosidase during subsequent recovery. By contrast, constitutive enzyme synthesis in recovering cells is normal. Even though no beta-galactosidase is made during recovery from this inhibition, a substantial quantity of beta-galactosidase mRNA (as determined by DNA-RNA hybridization) is made. The beta-galactosidase mRNA made in vivo is functional in vitro. It is capable of directing the in vitro synthesis of a portion of the NH2-terminal beta-galactosidase molecule (in the alpha portion of the molecule). However, this protein is not made in vitro. It is concluded that the beta-galactosidase mRNA that is made during recovery from protein synthesis inhibition, although apparently at least partly normally transcribed in vivo and functional in vitro cannot be translated under these conditions in vivo.     

水稻苗床土壤调酸后对土壤酶活性及一些营养元素的影响

水稻苗床土壤调酸后对土壤酶活性及一些营养元素的影响唐咏,梁成华,张中原,李焕珍（沈阳农业大学,１１０１６１）（沈阳市土肥工作站,１１００３４）ＥｆｆｅｃｔｓｏｆＳｏｉｌＡｃｉｄｉｆｉｃａｔｉｏｎｏｎＥｎｚｙｍｅＡｃｔｉｖｉｔｉｅｓａｎｄＮｕｔｒｉｅｎ...     

Regulation of Claspin degradation by the ubiquitin-proteosome pathway during the cell cycle and in response to ATR-dependent checkpoint activation

Claspin is involved in ATR-dependent activation of Chk1 during DNA replication and in response to DNA damage. We show that degradation of Claspin by the ubiquitin-proteosome pathway is regulated during the cell cycle. Claspin is stabilized in S-phase but is abruptly degraded in mitosis and is absent from early G(1) cells in which the phosphorylation of Chk1 by ATR is abrogated. In response to hydroxyurea, UV or aphidicolin, Claspin is phosphorylated in the Chk1-binding domain and its protein levels are increased in an ATR-dependent manner. Thus, the Chk1 pathway is regulated through both phosphorylation of Claspin and its controlled degradation.