Sequence and type-specific immunogenicity of the amino-terminal region of type 1 streptococcal M protein

The NH2-terminal sequence of type 1 M protein was determined by automated Edman degradation of purified polypeptide fragments extracted from whole streptococci by limited digestion with pepsin. Three polypeptide fragments were purified by slab gel electrophoresis on sodium dodecyl sulfate (SDS) polyacrylamide followed by electroelution. The purified fragments migrated as 28-, 25-, and 23.5-kDa fragments, respectively. Each of the fragments inhibited opsonization of a diluted antiserum prepared in rabbits by immunization with whole type 1 streptococci. The amino-terminal sequences of the peptide fragments were confirmed by comparison with the primary structure predicted from the nucleotide sequence of the type 1 M protein structural gene. The 28-kDa fragment contained the NH2-terminal asparagine residue of the processed type 1 M protein, whereas the NH2-terminal sequences of the 25- and 23.5-kDa peptides began at residues 27 and 36, respectively. A seven-residue periodicity with respect to polar and nonpolar residues was observed beginning at residue 22 and, therefore, the secondary structural potential of type 1 M protein is similar to that reported for other M proteins. In contrast to the other M proteins, however, identical repeats were rare, the longest sequence identity consisting of a three-amino acid acid sequence Lys-Asp-Leu at positions 30-32 repeated once at positions 65-67. A 23-residue synthetic peptide of the amino-terminus of the type 1 M protein evoked opsonic antibodies against type 1 streptococci. These results indicate that the NH2-terminal region of type 1 M protein retains the secondary structural characteristics of other M serotypes. Moreover, it contains epitopes that evoke protective immune responses. Our studies may have bearing in the development of safe and effective vaccines against group A streptococcal infections.     

Regression of blood vessels precedes cartilage differentiation during chick limb development

We have previously investigated distinct areas of vascular regression in the developing vascular system of the chick limb bud. Avascular areas appear in a characteristic spatial and temporal pattern, and are correlated with the position of developing cartilage. In the present study, we examined limb-bud sections which had been double labeled for endothelial cells and developing cartilage in order to determine the relationship between the appearance of cartilage and the disappearance of capillaries. Endothelial cells, which specifically take up acetylated low-density lipoprotein (acLDL), were labeled by intravenously injecting fluorescent acLDL (DiIacLDL) into chick embryos at Hamburger and Hamilton stages 26-30. Avascular zones, which correspond to the developing digits, were clearly visible within the fluorescently labeled distal vasculature. The same sections were labeled with monoclonal antibodies specific for cartilage. We found that progressing avascularity in the digital regions was followed by increased staining for cartilage antigens in the same areas. Zones of avascularity always developed earlier than morphologically and immunologically detectable cartilage in all planes of section and were always larger than the areas of cartilage. These results demonstrate that blood vessels disappear in predictable areas prior to the overt differentiation of cartilage.     

Late enzymes of vindoline biosynthesis

From differentiated plants of Catharanthus roseus (L.) G. Don we have isolated a specific enzyme of the vindoline biosynthetic pathway catalysing the S-adenosylmethionine-dependent methylation of 11-O-demethyl-17-O-deacetyl-vindoline. The enzyme we named S-adenosyl-L-methionine : 11-O-demethyl-17-O-deacetylvindoline 11-O-methyltransferase. This transferase exhibits a high substrate specificity. Obviously the O-methylation at C-11 precedes the O-acetylation at the C-17 position during the biosynthesis of vindoline.A second enzyme was detected which hydrolyses the acetyl function of vindoline. The distribution of this acetylesterase in C. roseus plants demonstrates that the enzyme is not specifically associated with the vindoline distribution in the plant material. Most probably this enzyme plays no essential role in the biosynthesis of vindoline.     

Late enzymes of vindoline biosynthesis. Acetyl-CoA: 17-O-deacetylvindoline 17-O-acetyl-transferase

From differentiated plants of Catharanthus roseus (L.) G. Don, a specific enzyme was isolated and named acetyl-CoA : 17-O-deacetylvindoline 17-O-acetyltransferase, acting on the biosynthetic formation of the Aspidosperma type alkaloid vindoline.The enzyme shows a high selectivity towards different substrates. The acetyl-CoA-dependent transferase also catalyses the reverse reaction by hydrolysis of the 17-O-acetyl group of vindoline in the presence of free CoA. This enzyme is localized only in vindoline-containing plant parts, but was so far not detectable in cell suspension cultures of C. roseus. The enzyme allows the synthesis of labelled vindoline with high specific activity, applicable for instance as tracer for radioimmunoassays of vindoline.     

Expression of L3T4 molecules on Lyt-2+, class II-restricted antigen-specific T suppressor lymphocytes

Three bovine serum albumin-specific Lyt-2⁺ T suppressor (Ts) cell clones from CBA/J mice have been analyzed with regard to expression of L3T4 molecules. All three Ts-cell clones can be stained with monoclonal antibodies (mAb) to L3T4. Tested for the two clones restricted to recognition of E^k determinants, antigen-specific proliferation on antigen-presenting cells, but not the proliferation induced by conditioned medium can be inhibited by L314-specific mAb. In a similar way, Ts-cell cytolytic effector functions can be blocked by L3T4-specific mAb. Thus L3T4 structures seem to play a role in Ts-cell functions. Furthermore, the data support the view that L3T4 expression can be a property of class II-restricted T cells irrespective of their Lyt phenotype.     

Lineare Systeme mit gesteuerten statistischen Impulsquellen

Summary From the communication engineers point of view the paper deals with networks consisting of linear filters and a special sort of controlled statistical pulse generators (SIG). The SIG responds to an analog signal with a sequence of Dirac impulses, where the probability for an output impulse at a given time depends on the instantaneous value of the input signal only. In connection with linear filters, however, systems can be realized in which the whole past of the input determines the statistical structure of the output. Therefore systems consisting of linear filters and SIGs (SIG networks) become interesting as models of biological systems, because in biological information processing transformations from analog signals into pulse trains occur very often. An example concerning the application of SIG systems in behavioural sciences will be discussed in a subsequent paper. In the present paper a theoretical analysis of the SIG and SIG networks is carried out by means of Statistical Communication Theory and Theory of Stochastic Processes. It is shown that under certain conditions very complex SIG networks can be treated with Correlation Theory. For one case not satisfying these conditions a solution on the base of Markoff processes is given.

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Auszug aus einer von der Fakultät für Maschinenwesen und Elektrotechnik der Technischen Hochschule München genehmigten Dissertation.Herrn Prof. Dr.-Ing. H. Marko danke ich für das Interesse und die fördernde Kritik während des Entstehens der dieser Arbeit zugrundeliegenden Dissertation. Der Deutschen Forschungsgemeinschaft ist für die finanzielle Förderung der Untersuchungen zu danken. Die numerischen Berechnungen wurden auf der Rechenanlage TR4 des Leibniz-Rechenzentrums der Bayerischen Akademie der Wissenschaften durchgeführt.     

Is male back space limiting? An investigation into the reproductive demography of the giant water bug,Abedus indentatus (Heteroptera: Belostomatidae)

Because male giant water bugs in the subfamily Belostomatinae provide parental care by brooding eggs on their back, an accurate assessment can be made of both the actual and potential reproductive capacity of males. Two operational sex-ratio (OSR) indices were developed and empirically measured for a population of giant water bug, Abedus indentatus,in California. One index was based on reproductive rates measured in the laboratory; the other index was based on reproductive resources observed in the field. Both OSR indices suggest that the operational sex ratio fluctuates between maleskewed ratios in the summer and femaleskewed ratios in the winter. This pattern appears to be the consequence of two factors. First, the adult sex ratio is significantly female biased. Second, although males can outreproduce females at high ambient temperatures, the reverse is true at low temperatures. Possible reasons for the female-skewed adult sex ratio are examined, including differential recruitment, differential mortality, and sampling bias.