Defatting and Clarification of Protein Hydrolysates by Using Chitosan Solutions

The possibility of the use of small amounts of chitosan for defatting and clarification of protein solutions prepared by enzymatic hydrolysis was tested. The following treatment conditions were shown to be optimal: a chitosan concentration range, from 1.0 to 1.5 gram per kilogram raw weight; pH of the precipitation medium from 8.0 to 8.5; and duration of the incubation of the protein hydrolysate solution with chitosan, less than 1 h. The hydrolysate defatting grade was found to depend on the degree of chitosan deacetylation. A possible mechanism of the chitosan-induced effects was suggested. The use of chitosan allows the mass fraction of enzyme protein hydrolysates to be reduced fourfold to fivefold.     

Conditional Maximum Likelihood Estimation Following a Group Sequential Test

We consider estimation after a group sequential test. An estimator that is unbiased or has small bias may have substantial conditional bias (Troendle and Yu, 1999, Coburger and Wassmer, 2001). In this paper we derive the conditional maximum likelihood estimators of both the primary parameter and a secondary parameter, and investigate their properties within a conditional inference framework. The method applies to both the usual and adaptive group sequential test designs. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Evolutionary significance of morphogenetic mechanisms

Different approaches to interpretation of ontogenesis are compared. The importance is emphasized of Ber’s theory of developmental patterns and the law of embryonic similarity. The significance of evolutionary rationalization of morphogenetic mechanisms is discussed (V.N. Beklemishev, V.A. Dogel’ and O.M. Ivanova-Kazas). There are two main pathways of rationalization of morphogenetic mechanisms: by means of epithelial morphogenesis and at the expense of oligocellular primordia (V.N. Beklemishev). When the developmental plans of the taxonomical types are determined, it is important to take into consideration the diversity of morphogenetic mechanisms within a given group in order to reveal morphological spectrums of morphogenetic mechanisms. A comparison of morphogenetic spectrums in different groups provides a wide evolutionary picture and helps us to reconstruct the phylogeny. Influence of morphogenetic mechanisms on the structure of definitive forms is demonstrated: construction technologies determine types of organs, anatomical and histological systems, and even symmetrical features of organisms and their complex parts.     

Oldest shrimp and associated phyllocarid from the Lower Devonian of northern Russia

A mass occurrence of schooling, weakly sclerotized eocaridid shrimps in the Early Devonian pelagic environment of northern Russia suggests that the body-plan of the Eumalacostraca originated as an adaptation to swimming in the open sea. They probably replaced their ecological analogues, the archaeostracan phyllocarids Caryocaris , as a consequence of the rebuilding of the global marine environment during the later Ordovician. This may explain the rarity of the eumalacostracans in the Devonian and the difficulty with documenting their links with the archaeostracans. The new eocaridid shows similarities to the Carboniferous Anthracophausia in the general appearance and weak sclerotization of the carapace and appendages, but lacks its derived characters. The morphology of the pleural lobes, which have minute spines, is the only identified distinguishing character of the proposed new genus and species Archangeliphausia spinosa gen. et sp. nov. Its carapace was probably firmly connected dorsally with the thoracic segments. The only associated fossils of the assemblage represent a bizarre archaeostracan Pechoracaris aculicauda gen. et sp. nov., with a weakly sclerotized carapace lacking any hinge or rostral plates but with reduced furca, an extremely long caudal spine and pleopods transformed into spines.  © 2004 The Linnean Society of London, Zoological Journal of the Linnean Society , 2004, 142 , 83–90.     

Localization of sources of thalamic inputs into the sensorimotor cortex in the rabbit using retrograde axonal transport technique

It was shown that the rabbit sensorimotor cortex received afferent fibers from neurons located in the specific, nonspecific, and association thalamic nuclei using the retrograde axonal transport technique. The distribution, dimensions, and shape of the somata of relay neurons spread through the thalamic nuclei were analyzed. The total number of neurons sending out thalamo-sensorimotor-cortical fibers was calculated and the coordinates of loci with the highest density of these cells in each thalamic nucleus were identified. Multipolar and stellate cells with somata measuring 12–20 µm and 10–15 µm in diameter, respectively, prevailed amongst relay neurons. Amongst the specific nuclei, the majority of afferent fibers are sent out by the ventrolateral, ventral anterior, and anterior ventral nuclei. A comparable number of afferent fibers are sent out by the mediodorsal and paracentral nuclei; these split up among the association nuclei and paracentral nuclei, respectively. It is suggested that afferents from many different groups of thalamic nuclei are essential for the sensorimotor cortex to participate in thalamocortical interaction.Institute of Higher Nervous Activity and Neurophysiology, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 19, No. 1, pp. 87–94, January–February, 1987.     

Reordering of scratch generator efferent activity produced by stimulating hindlimb skin afferents in decerebrate immobilized cat

Reordering of the parameters of motor activity produced in the scratch generator by regular electrical stimulation of the ipsilateral hindlimb muscle nerve during different limb positions was investigated in decerebrate immobilized cats. Brief short latency inhibition of currently occurring motor activity was produced in response to stimulation, which did not cause an overall shift in the relationship between the intensity of aiming and scratching motion. Changes in cycle duration and intensity of these activities were phase-locked. Speculations were made on the functional role of the phase-locked nature of motor activity remodeling. The possible existence within the scratch generator of a model of the afferent inflow entering the spinal cord during true scratching is suggested.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 19, No. 3, pp. 382–390, May–June, 1987.     

Suitability of aspenwood biologically delignified with Pheblia tremellosus for fermentation to ethanol or butanediol

Summary Enzymatic conversion of lignocellulosic material to fuels and chemicals depends on a initial pretreatment to render the cellulose more susceptible to enzymatic attack. Biological delignification of aspenwood with the fungus Phlebia tremellosus was compared to steaming as a pretreatment method.The biologically delignified aspenwood (BDA) had a high pentosan content and did not contain inhibitors of enzymatic hydrolysis or subsequent fermentation. In contrast, the steamed aspenwood required a water extraction step to remove the inhibitory material and this step also removed most of the pentosan. The yield of treated material was 90% from biological delignification and 70% from steaming.The cellulose in the BDA was less accessible to the cellulase enzymes than the steamed aspenwood. Combined hydrolysis and fermentation with Saccharomyces cerevisiae gave a lower yield of ethanol from BDA than from the steamed aspenwood, but the yields based on the weight of substrate before pretreatment were comparable. Combined hydrolysis and fermentation with Klebsiella pneumoniae gave higher yields of butanediol from BDA than from steamed aspenwood, because Klebsiella can ferment the xylose which was present in the biologically treated aspenwood. Trichoderma harzianum produced lower levels of cellulase enzymes when grown on BDA than when grown on steamed aspenwood and this was related to the xylan found in the biologically treated material.Abbreviations BDA biologically delignified aspenwood - SEA-WI steam-exploded, water-extracted aspenwood - AI-SEA-WI acid-impregnated, steam-exploded, water-extracted aspenwood - CHF combined hydrolysis and fermentation - FP filter paper     

Tumulduria incomperta and the case for Tommotian trilobites

The enigmatic fossil Tumulduria incomperta Missanhevsky 1969 from the basal Tommotian Stage at 'Dvortsy' on the Aldan River, Siberian Platform, is reinvestigated in light of the report (Fedorov et al. 1979, Dokl. AN SSSR 249) of trilobite remains from the same beds. Comparisons of these supposed trilobites with old and new collections from 'Dvortsy' leave no doubt that they are identical to Tumulduria incomperta. Tumulduria is represented by phosphatic plates with a crude bilateral symmetry, consisting of a central longitudinal rounded ridge flanked by flat lateral portions. They are built of growth lamellae overlapping each other along the axis of symmetry. The surface carries prominent transverse folds and lamellar terminations. There is considerable morphological variation, and the similarity of some specimens to trilobites is only superficial. Tumulduria is interpreted as a bilaterally symmetrical metazoan with a dorsal protective plate; it probably represents a short-lived group that left no descendants.     

A test using cultured cells with induced mixed-function oxygenase in the unscheduled DNA synthesis assay for detecting promutagens/procarcinogens

The human FL cell line contains very low levels of constitutive AHH activity, but it could be greatly induced by NE, beta-NF and 3-MC, and induced slightly by PB. When two different types of inducer, for example, 3-MC and PB or 3-MC and NE were given in combination, an additive inductive effect was not observed. Both the constitutive and induced AHH in FL cells have characteristics of MFO, namely, NADPH-dependence and CO-sensitivity. The fact that the constitutive and induced AHH in FL cells could be inhibited by a known hydroxylase inhibitor 7,8-BF indicated that the AHH in FL cells belongs to the cytochrome P-448 dependent MFO type. After removal of inducer from the medium, the induced AHH activity remained at a high level for at least 24-36 h. By using AHH-induced FL cells in the UDS assay system for the detection of promutagens/procarcinogens, we found that AFB1 and 3-MC did not induce a UDS reaction in uninduced FL cells, while in beta-NF induced cells, 10(-6)-10(-4) M AFB1 and 10(-7)-10(-6) M 3-MC elicited a very significant UDS reaction, which was concordant with the results obtained in the UDS assay system using HeLa cells or FL cells supplemented with liver microsomes or using primary cultured hepatocytes as indicator cells. B(a)P elicited the UDS reaction at concentrations of 10(-6)-10(-3) M in beta-NF induced cells, whereas 10(-4)-10(-3) M was required in uninduced cells. The results above indicate that this new design is feasible, but further study is needed to assure its accuracy.