Breeding,production and marketing of golden tench (<Emphasis Type="Italic">Tinca tinca</Emphasis> (L.)) in Gan Shmuel Fish Breeding Center,Israel

A first attempt to introduce tench (Tinca tinca (L.)) to Israel, followed by comparative growth experiments, was carried out in 1947. A batch of 200 fingerlings, which were supposed to serve later as brood fish, was imported from Switzerland to Fish Culture Experimental Station at Sdeh Nahum. However, after 2 years tench were considered unsuitable for culturing in Israel and the trials were abandoned. Two factors affected negatively these historically early trials: (1) Tench was just second exotic species introduced to Israel some years after introduction of the common carp, and the Israeli fish farming expertise at that time was low. (2) The Independence War temporarily delayed advancement of aquaculture. A second introduction of tench was performed in 1992, when a golden mutant of tench was imported to Gan Shmuel Fish Breeding Center (GS-FBC) from the Research Institute of Fish Culture and Hydrobiology at Vodňany, Czech Republic. Currently, GS-FBC is the only Israeli fish hatchery that maintains golden tench as a part of breeding program as well as a number of other varieties of ornamental fish and species, all of them produced mostly for export. Tench (800–1,000 g) females are maintained separately from males, in order to prevent uncontrolled reproduction. Routinely, in April, the fish are transferred indoors and induced to spawn artificially with a single injection of GnRH synthetic analog—DAGIN. Dry method of stripping is used to obtain eggs and sperm. After fertilization the sticky eggs are spread in a single layer on walls of 230 dm³ cylindrical incubators provided with conical bottom, or they are degummed using a solution of milk/water. At a water temperature of 24°C, hatching (70% hatching rate) occurs 36–40 h after fertilization. The larvae absorb their yolk sac 2–3 days after fertilization and they start feeding on small size (200 μm) Artemia nauplii. At the age of 7–10 days, if fry are retained indoors, they are fed with regular size Artemia and starter feed, or are released into a nursing 0.5–1.0 ha pond. Usually, the fish are grown to the marketing size (5–15 cm) and exported abroad, mainly to Europe. About 100,000 golden tench fingerlings, with a total value of € 40,000 are produced and marketed annually.     

The expression of genes involved in parasitism by Trichoderma harzianum is triggered by a diffusible factor

The mycoparasite Trichoderma harzianum has been extensively used in the biocontrol of a wide range of phytopathogenic fungi. Hydrolytic enzymes secreted by the parasite have been directly implicated in the lysis of the host. Dual cultures of Trichoderma and a host, with and without contact, were used as means to study the mycoparasitic response in Trichoderma. Northern analysis showed high-level expression of genes encoding a proteinase (prb1) and an endochitinase (ech42) in dual cultures even if contact with the host was prevented by using cellophane membranes. Neither gene was induced during the interaction of Trichoderma with lectin-coated nylon fibres, which are known to induce hyphal coiling and appressorium formation. Thus, the signal involved in triggering the production of these hydrolytic enzymes by T. harzianum during the parasitic response is independent of the recognition mediated by this lectin-carbohydrate interaction. The results showed that induction of prb1 and ech42 is contact-independent, and a diffusible molecule produced by the host is the signal that triggers expression of both genes in vivo. Furthermore, a molecule that is resistant to heat and protease treatment, obtained from Rhizoctonia solani cell walls induces expression of both genes. Thus, this molecule is involved in the regulation of the expression of hydrolytic enzymes during mycoparasitism by T. harzianum.     

Muscle spindles in muscle control

In a previous paper (Inbar, 1972/III) a new adaptive model was proposed for muscular control. According to that scheme muscle spindles (MS) supply continuous information about the system dynamics. In the present study integral pulse frequency modulation (IPFM) is used to correlate MS afferent signals, recorded from frog sartorius muscle, to the same muscle dynamics, in order to establish the feasibility of the proposed MS role in the adaptive muscle model.     

A Novel Solution for the High Defibrillation Threshold in Patients with a DF-4 Lead: Adding a High Voltage Adaptor/Splitter

A high defibrillation threshold occurs in approximately 6% of implants. The defibrillation threshold can be improved by addition of a defibrillation lead. However, the DF-4 high energy ICD header precludes the addition of a defibrillation lead. Here we report on use of a new high voltage adaptor/splitter that enables the addition of an extra defibrillation lead.     

Isolation of plasma membrane fragments and vesicles from ascites fluid of lymphoma-bearing mice and their possible role in the escape mechanism of tumors from host immune rejection

Summary Plasma membranes, generated in vivo by actively growing YAC lymphoma cells, were isolated from cell-free ascites fluid of lymphoma-bearing mice. Partial purification of the ascites fluid (AF) by means of ultracentrifugation resulted in the identification of two main fractions: (a) membrane fragments (AFM _s ) and (b) membrane vesicles (AFM _p ). Electron microscopy studies, polyacrylamide gel electrophoresis, marker enzymes, and binding capacity of radioactive lectins, have indicated that these membranes are released from the cell surface of YAC lymphoma cells, presumably by a shedding-off mechanism.In vitro studies have demonstrated that the isolated membranes can specifically inhibit the association of normal macrophages and YAC lymphoma cells. In vivo studies have shown that these membranes can immunize against YAC tumors if injected intramuscularly or subcutaneously into adult mice. The results indicate that the ascites fluid membranes bear tumor-specific antigenic determinants.Our results suggest that in vivo shedding of plasma membrane fragments or of membrane vesicles by actively growing YAC lymphoma cells may induce a self-protection of ascites tumors from host immune rejection.Abbreviations YAC= Moloney-virus-induced lymphoma cells grown in A-strain mice - AF= ascites fluid of YAC lymphoma-bearing mice - AFM_s and AFM_p= membrane fragments and vesicles isolated from AF - PBS= phosphate-buffered saline - Con A= Concanavalin A     

13C-NMR, 1H-NMR and gas-chromatography mass-spectrometry studies of the biosynthesis of 13C-enriched L-lysine by Brevibacterium flavum

The basic metabolic pathways of lysine biosynthesis in Brevibacterium flavum, a strain which excretes excessive amounts of L-lysine, have been followed by using two 13C-labeled precursors. 13C- and 1H-NMR spectroscopies in conjunction with gas chromatography mass spectrometry (GC-MS) have revealed the various metabolic pathways leading to L-[13C]lysine. Discrete metabolic pathways give rise to distinct labeling patterns. L-Lysine resulting from [1-13C]glucose fermentation is relatively specifically labeled: L-[3,5-13C]lysine is the main product. Experimental and theoretical approaches based on the 13C-enrichment values of intracellular glutamate, a major intermediate metabolite, allowed us to assess the relative contribution of the major metabolic pathways forming lysine. The labeling pattern of glutamate reflects the isotope distribution in 2-oxoglutarate. When [2-13C]acetate is used as the sole carbon source in the culture, the energy-producing steps of the Krebs cycle are essential. The higher activity of the Krebs cycle, when endogenous carbohydrates are exhausted from the culture, is indicated by the increased 13C enrichment in C-1 of lysine and reveal a high content of isotopomers of four, five and six 13C atoms in the lysine molecule, pointing out that the four-carbon intermediates of the cycle are being derived from the glyoxylate shunt pathway. Such a phenomenon does not occur in glucose fermentation. GC-MS analyses of 13C enrichments and isotopomer distributions in metabolites and end products are in good agreement with the predicted contribution of each metabolic pathway. This new methodological approach of combined NMR and GC-MS has been demonstrated to be applicable to various other metabolic studies.