The effect of temperature and crowding on midgut amylolytic activity in Tenebrio molitor adults

The effect of two constant temperatures (23°C and 28°C), mixed group (5 + 5), and isolation on the midgut amylolytic activity during adult development of Tenebrio molitor has been investigated in vitro. Higher temperatures (28°C) and mixed groups stimulate the rate of midgut amylolytic activity. After attaining the maximal level, the amylolytic activity shows fluctuations. The possible role of hormones and primer pheromones in the control of the midgut amylolytic activity in T. molitor adults is discussed.     

A combined scanning and transmission electron microscopic study and electron probe microanalysis of human pineal acervuli

Summary Untreated, decalcified and trypsinized acervuli from human pineal bodies were studied with the scanning and transmission electron microscope as well as by electron probe microanalysis. The mulberry-like acervuli are composed of a various number of spherical lobes (135–800 m) between which clustered groups of globuli (4–14 urn in diameter) are observed. The acervular lobes are very probably formed by an aggregation of these globuli. Small round particles 125–500 Å in diameter are observed on the surface of the pineal concretions. These are not influenced by either decalcification or trypsin treatment. The acervular mineral corresponds morphologically to hydroxyapatite. The electron probe microanalysis reveals the existence of calcium and phosphorus as main components of the acervuli. Small quantities of magnesium and strontium were also detected.Dedicated to Professor Berta Scharrer on the occasion of her 70th birthdayWith the technical assistance of Mr. P.A. MilliquetThe author wishes to thank Mr. Bauer and Mr. Fryder (Nestec SA, La Tour de Peilz) for the use of the Cambridge Stereoscan electron microscope and Dr. T. Jalanti (C.M.E., Lausanne) for his help with the use of the X-ray microanalyser     

The application of an averaging method to intermittently modified and endogenously generated spike activities of neurons in mollusc ganglia

The averaging method was applied for the analysis of the effect of intermittent light as well as for the analysis of the spontaneous spike activities of burster neurons in Helix pomatia and Aplysia depilans ganglia. Owing to such analyses by means of which the unwanted effects of permanently present noise (i.e., irregular frequency modulation of neuron impulse activity) were diminished, the dynamics of the neurons reaction to light and the longer time effects of intermittent illumination on neurons spontancous activity could be observed. The functional characteristics of burster neurons were determined by averaging and the least squares and equalization methods. The results were presented in the table and in two average curves which are asymmetrical with a horizontal asymptote. From these data it was concluded that the dynamics of the spontaneous activity of the two burster neurons in both specia is similar. The possibilities and limitations of the method in physiological analyses are discussed.     

Eiweißkristalloide inOpuntia inermis

Zusammenfassung In den Epidermiszellen der Blätter vonOpuntia inermis wurden neben den X-Körpern und Eiweißspindeln auch echte Eiweißkristalle in Form rhombenförmiger Plättchen gefunden. Diese Kristalle sind vermutlich im Zellsafte lokalisiert.Die spindelhaltigen Exemplare vonOpuntia inermis unterschieden sich auch dadurch von anderen spindelführenden Kakteen, daß sie auch in Schließzellen Eiweißspindeln enthielten. Das Ausbleiben der Eiweißspindeln in den Schließzellen der Kakteen ist demnach keine regelmäßige Erscheinung.Prof. Dr. V.Vouk zum 70. Geburtstag gewidmet.     

(鼲)属(啮齿目,仓鼠科)同域分布物种形态学鉴别特征组的筛选

现有的分类系统尚缺乏可用于减少䶄属物种种间鉴定不确定性的形态学鉴别特征。鉴于此,本研究旨在筛选出能够对同域分布的棕背䶄（Myodes rufocanus）, 红背䶄（M. rutilus）和堤岸䶄（M. glareolus）进行可靠鉴定的头骨形态指标和方法。为了达到以上目的,本文一方面筛选出能够用于种间鉴别的头骨和齿列形态特征,另一方面提出可用于鉴别以上三个物种的计算公式。对不同研究者提出来用于鉴别以上三个同域分布物种的35个特征进行筛选。头骨形态测量数据的获取需要花费较长的时间,而且结果变异很大。在本研究中,在分析中剔除15个形态特征,20个相对保守的特征被选择用于分析（包括来自头盖骨、牙齿和头骨其它部位的特征）。在20个特征中,有8个特征被选择出来,并使用Statistica 10 计算出判别公式。这些特征使准确鉴定不同个体各自所属种类成为可能。     

A new approach for activation of the kiwifruit cysteine protease for usage in in-vitro testing

Molecular Biology Reports - Actinidin (Act d 1), a highly abundant cysteine protease from kiwifruit, is one of the major contributors to the development of kiwifruit allergy. Many studies have...     

Cytotoxic activities of Hypericum perforatum L. extracts against 2D and 3D cancer cell models

Cytotechnology - Six extracts were obtained from plant species Hypericum perforatum L., collected at Samsun in Turkey. The aim of this study was to examine the mechanisms of the anticancer activity...     

Influence of membrane-cortex linkers on the extrusion of membrane tubes

The cell membrane is an inhomogeneous system composed of phospholipids, sterols, carbohydrates, and proteins that can be directly attached to underlying cytoskeleton. The protein linkers between the membrane and the cytoskeleton are believed to have a profound effect on the mechanical properties of the cell membrane and its ability to reshape. Here, we investigate the role of membrane-cortex linkers on the extrusion of membrane tubes using computer simulations and experiments. In simulations, we find that the force for tube extrusion has a nonlinear dependence on the density of membrane-cortex attachments: at a range of low and intermediate linker densities, the force is not significantly influenced by the presence of the membrane-cortex attachments and resembles that of the bare membrane. For large concentrations of linkers, however, the force substantially increases compared with the bare membrane. In both cases, the linkers provided membrane tubes with increased stability against coalescence. We then pulled tubes from HEK cells using optical tweezers for varying expression levels of the membrane-cortex attachment protein Ezrin. In line with simulations, we observed that overexpression of Ezrin led to an increased extrusion force, while Ezrin depletion had a negligible effect on the force. Our results shed light on the importance of local protein rearrangements for membrane reshaping at nanoscopic scales.