Pre- and post-mortem use of grape seed extract in dark poultry meat to inhibit development of thiobarbituric acid reactive substances

Diets containing grape seed extract (GSE)-control, GSE [low GSE, low GSE + methionine, high GSE, and high GSE + methionine], or alpha-tocopherol-were fed to broiler chicks to estimate the antioxidative activity of GSE in processed meat. GSE was detrimental to the growth of chicks, and methionine did not reverse the detrimental effect. GSE with 85.4 g of gallic acid equiv/100 g (GAE 85.4) was added to ground dark turkey meat to obtain treatments with no GSE, 1.0% GSE, and 2.0% GSE and then processed as unsalted or salted and unheated or heated. Processed treatments were analyzed for thiobarbituric acid reactive substances (TBARS) and percent expressible moisture (%EM). GSE at 1.0 and 2.0% decreased TBARS values nearly 10-fold as compared to the control. GSE (1.0%) had a %EM value significantly greater than that of the control. GAE 85.4 decreased TBARS values more than GAE 88.9.     

Structure of Galphaq-p63RhoGEF-RhoA complex reveals a pathway for the activation of RhoA by GPCRs

The guanine nucleotide exchange factor p63RhoGEF is an effector of the heterotrimeric guanine nucleotide-binding protein (G protein) Galphaq and thereby links Galphaq-coupled receptors (GPCRs) to the activation of the small-molecular-weight G protein RhoA. We determined the crystal structure of the Galphaq-p63RhoGEF-RhoA complex, detailing the interactions of Galphaq with the Dbl and pleckstrin homology (DH and PH) domains of p63RhoGEF. These interactions involve the effector-binding site and the C-terminal region of Galphaq and appear to relieve autoinhibition of the catalytic DH domain by the PH domain. Trio, Duet, and p63RhoGEF are shown to constitute a family of Galphaq effectors that appear to activate RhoA both in vitro and in intact cells. We propose that this structure represents the crux of an ancient signal transduction pathway that is expected to be important in an array of physiological processes.     

Anwendung numerisch-taxonomischer Methoden bei Kulturpflanzen

Zusammenfassung Es wird eine Übersicht über die Anwendung numerisch-taxonomischer Methoden bei Kulturpflanzen gegeben. Diese werden bei Kulturpflanzen bisher nur wenig benutzt.Eine bessere theoretische Durchdringung der numerisch-taxonomischen Methoden scheint erforderlich. Es wird auf Anwendungsmöglichkeiten numerischtaxonomischer Methoden bei Kulturpflanzen hingewiesen.

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Use of numerical taxonomic methods in cultivated plants

Summary A review is given on the use of numerical taxonomic methods in cultivated plants. Up till now these methods have been applied to cultivated plants only to a limited extent.A more thorough study of the theory of numerical taxonomy seems necessary. Some possibilities of application of numerical taxonomic methods to cultivated plants are briefly discussed.

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Herrn Prof. Dr. Dr. h. c. mult. H.Stubbe aus Anlaß der 80. Wiederkehr seines Geburtstages gewidmet.     

Resistenzeigenschaften im Gersten- und Weizensortiment Gatersleben 27. Prüfung von Gersten auf ihr Verhalten gegenüber Gerstengelbmosaik-Virus (barley yellow mosaic virus),Drechslera teres (Sacc.) Shoem. undPuccinia hordei Otth

Zusammenfassung Unter 133 Gersten aus dem Gaterslebener Sortiment erwiesen sich 113 als anfällig und 20 als resistent gegen Gerstengelbmosaik-Virus (barley yellow mosaic virus). Weitere 22 Gersten mit Virusresistenz waren teilweise gleichzeitig gegenPuccinia hordei resistent.

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Resistance in the Gatersleben barley and wheat collection. 27. Testing of barley for reaction to barley yellow mosaic virus (BaYMV),Drechslera teres (Sacc.) Shoem. andPuccinia hordei Otth

Summary Out of 133 barleys were classified 113 as susceptible (table 1) and 20 as resistant to barley yellow mosaic virus (table 2). Of further 22 barleys with BaYMV resistance were some resistant towardsPuccinia hordei too (table 3).

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27. (barley yellow mosaic virus),Drechslera teres (Sacc.) Shoem. Puccinia hordei Otth

133 113 (barley yellow mosaic virus) 20 — , 22 - , , Drechslera teres Puccinia hordei.

     

Identification of Hedgehog pathway components by RNAi in Drosophila cultured cells

Classical genetic screens can be limited by the selectivity of mutational targeting, the complexities of anatomically based phenotypic analysis, or difficulties in subsequent gene identification. Focusing on signaling response to the secreted morphogen Hedgehog (Hh), we used RNA interference (RNAi) and a quantitative cultured cell assay to systematically screen functional roles of all kinases and phosphatases, and subsequently 43% of predicted Drosophila genes. Two gene products reported to function in Wingless (Wg) signaling were identified as Hh pathway components: a cell surface protein (Dally-like protein) required for Hh signal reception, and casein kinase 1alpha, a candidate tumor suppressor that regulates basal activities of both Hh and Wg pathways. This type of cultured cell-based functional genomics approach may be useful in the systematic analysis of other biological processes.     

Minimum alveolar concentration of isoflurane in green iguanas and the effect of butorphanol on minimum alveolar concentration

OBJECTIVE: To determine minimum alveolar concentration (MAC) of isoflurane in green iguanas and effects of butorphanol on MAC. DESIGN: Prospective randomized trial. ANIMALS: 10 healthy mature iguanas. PROCEDURE: in each iguana, MAC was measured 3 times: twice after induction of anesthesia with isoflurane and once after induction of anesthesia with isoflurane and IM administration of butorphanol (1 mg/kg [0.45 mg/lb]). A blood sample was collected from the tail vein for blood-gas analysis at the beginning and end of the anesthetic period. The MAC was determined with a standard bracketing technique; an electrical current was used as the supramaximal stimulus. Animals were artificially ventilated with a ventilator set to deliver a tidal volume of 30 mL/kg (14 mL/lb) at a rate of 4 breaths/min. RESULTS: Mean +/- SD MAC values during the 3 trials (2 without and 1 with butorphanol) were 2.0 +/- 0.6, 2.1 +/- 0.6, and 1.7 +/- 0.7%, respectively, which were not significantly different from each other. Heart rate and end-tidal partial pressure of CO2 were also not significantly different among the 3 trials. Mean +/- SD heart rate was 48 +/- 10 beats/min; mean end-tidal partial pressure of CO2 was 22 +/- 10 mm Hg.There were no significant differences in blood-gas values for samples obtained at the beginning versus the end of the anesthetic period. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that the MAC of isoflurane in green iguanas is 2.1% and that butorphanol does not have any significant isoflurane-sparing effects.     

Impact of soil texture on temporal and spatial development of osmotic‐potential gradients between bulk soil and rhizosphere

Solute transport from the bulk soil to the root surface is, apart from changes in soil moisture and plant nutrient uptake, a prerequisite for changes in soil osmotic potential (Ψ_o). According to the convection‐diffusion equation, solute transport depends on a number of parameters (soil moisture–release curve, hydraulic conductivity, tortuosity factor) which are functions of soil texture. It was thus hypothesized that soil texture should have an effect on the formation of Ψ_o gradients between bulk soil and the root surface. The knowledge about such gradients is important to evaluate water availability in the soil‐plant‐atmosphere continuum (SPAC). A linear compartment system with maize grown under controlled conditions in two texture treatments (T1, pure sand; T2, 80% sand, 20% silt) under low and high initial application of salts (S1, S2) was used to measure the development of Ψ_o gradients between bulk soil and the root surface by microscale soil‐solution sampling and TDR sensors. The differences in soil texture had a strong impact on the formation of Ψ_o gradients between bulk soil and the root surface at high and low initial salt application rate. At high initial salt application, a maximum osmotic‐potential gradient (ΔΨ_o) of –340 kPa was observed for the texture treatment T2 compared to ΔΨ_o of –180 in T1. The steeper gradients in osmotic potential in treatment T2 compared to T1 corresponded to higher cumulative water consumption in this treatment which can partly be explained by higher soil hydraulic conductivity in the range of soil matric potentials covered during the duration of the experiments. Differences between texture treatments in Ψ_o at the root surface did not result in differences in plant‐water relations measured as gas‐exchange parameters (transpiration rate, water‐use efficiency) and leaf osmotic potential. If soil osmotic and matric potential are regarded as additive in calculating the driving force for water movement from the soil into the root, the observed differences in water flux between treatments cannot be explained.     

Effect of transfer time,temperature, and size on burrowing capacity of juvenile clams,Mulinia edulis,from hatchery

Studies under laboratory and field conditions have shown that juvenile Mulinia edulis clams measuring 5–15 mm are able to tolerate transfer times of over 24 hr and burrow successfully. Burrowing generally followed an asymptotic curve over time, with a rapid initial phase for smaller juveniles, which slowed over time. In laboratory conditions, at low temperatures (8°C), juvenile burrowing was initially rapid (50–70% at first 2 min). In summer temperatures (15.5°C), the burrowing capacity of three sizes of juvenile clams was tested. Size determines differences in burrowing dynamics, where juveniles of 8.9 mm shell length (SL) take longer to burrow than smaller juveniles (4.9 and 6.3 mm SL). For longer transfer times in laboratory conditions (>12 hr), burrowing was slower. The results indicate a faster burrowing rate in smaller (<10 mm) juvenile clams than in larger ones. Transfer times over 24 hr in field experiments show burrowing levels of over 50% after a 60‐min evaluation, with larger juveniles (>10 mm) requiring longer for burrowing. Based on our results, we suggest sending seeds out to grow in natural environments at SL <10 mm, temperatures below 12°C, and transfer times shorter than 12 hr. These results are valuable for improving future transfer techniques from hatchery to growout for small‐scale aquaculture of this new native species in South America.