Expanding abdominal cuticle in the bug Rhodnius and the tick Boophilus

The abdominal cuticles of Rhodnius prolixus (fifth instar) and Boophilus microplus (adult female) expand dramatically and rapidly during feeding. In the unfed stage of both species the epicuticle of the abdomen is deeply folded, and when rapid stretching takes place the epicuticle unfolds and the underlying procuticle stretches so that the thickness of the cuticle is halved. The cuticles contained only trace amounts of protein soluble in water and aqueous KCl but substantial quantities were extracted with 7 M aqueous urea. The proteins were analysed for their amino acid composition and investigated by gel electrophoresis and isoelectric focusing.In solubility, amino acid composition, molecular weight distribution, and isoelectric points, the proteins isolated from both species resembled one another closely. They had higher molecular weights and higher isoelectric points than did the proteins from flexible, non-stretching cuticles and unlike them had high alanine and histidine and low aspartic acid and glutamic acid contents. Their amino acid composition was very similar to that of the whole cuticle. The proteins were not associated with neutral sugars. Both the Rhodnius and Boophilus cuticles had low chitin contents, 11·2 and 3·8% respectively (on a water-free basis). The composition of the cuticles and the properties of the proteins are discussed in relation to the stretching which they undergo.     

Foregut morphology and ontogeny of the mud crab Dyspanopeus sayi (Smith, 1869) (Decapoda,Brachyura, Panopeidae)

The morphology of the foregut of the Say's mud crab Dyspanopeus sayi was described in adults and larvae. The ossicle system was illustrated based on a staining method with Alizarin-Red. The gastric teeth and cardio-pyloric valve were dissected and examined using optical and scanning electron microscopy. In the adults, the morphology of ossicles and gastric teeth of D. sayi is very similar to the related species Rhithropanopeus harrisii. The foregut of first zoea (ZI) presented a functional cardio-pyloric valve while the filter press was lacking. The filter press was observed in the pyloric chamber from ZII. The most significant changes in morphology take place after metamorphosis from ZIV to megalopa, including the occurrence of the gastric mill. The organization and morphology of many megalopal foregut ossicles are recognizable in the adult phase, although the morphology of the gastric teeth differs from the morphology of adults. A correlation of gastric mill structures with food preferences and their contribution to the phylogeny are briefly discussed.     

The role of a putative peroxisomal-targeted epoxide hydrolase of Nicotiana benthamiana in interactions with Colletotrichum destructivum, C. orbiculare or Pseudomonas syringae pv. tabaci

Motif analysis among 30 EH1 and EH2 epoxide hydrolases from Solanaceaeous plants showed differences primarily in the lid region around the catalytic site. Based on in silico models of 3D structures, EH1 proteins lack a catalytic triad because of the orientation of one of the conserved lid tyrosines, while the orientation of that tyrosine in EH2 proteins fomed a catalytic triad inside a hydrophobic tunnel. Two similar EH2 protein genes from Nicotiana benthamiana, NbEH2.1 and NbEH2.2, have a predicted peroxisomal targeting sequence, catalytic triad, and structural similarities to a potato cutin monomer-synthesizing epoxide hydrolase. NbEH2.1 expression increased with infections by the hemibiotrophs, Colletotrichum destructivum, Colletotrichum orbiculare or Pseudomonas syringae pv. tabaci only during their biotrophic phases, while there was only a slight increase during the hypersensitive response to P. syringae pv. tabaci (avrPto). In contrast, among the four pathogens, NbEH2.2 expression increased only in response to P. syringae pv. tabaci. Virus-induced gene silencing of NbEH2.1 significantly affected only the interaction with C. destructivum, resulting in a delay in the appearance of necrosis that may be related to its biotrophic phase being restricted to single epidermal cells, which is unique among these pathogens. These results differed from that of a previously reported EH1 gene of N. benthamiana for these interactions, demonstrating specialization among EH genes in basal resistance.     

Quantitative isolation of native chitin from resistant structures of Sordaria and Ascaris species

A procedure for the quantitative isolation of native chitin from resistant biological structures is developed utilizing ozone and neutralized hydrogen peroxide ethylenediaminetetraacetic acid. These reagents permit extraction of the chitinous component at a neutral pH without any preliminary cell disruption or extensive fractionation, thereby conserving the cell wall integrity and structure. The resulting product is essentially free of protein and is greatly enriched in chitin content, the exact purity of which depends upon the nature of the particular chitin source. The chitin polymer is recovered in a highly N-acetylated form and is readily identified with a standard chitin reference by physical characterization, infrared spectroscopy, enzymatic hydrolysis, and glucosamine assay.     

Endodermal secretion of chitin in the 'cuticle' of the earthworm gizzard

The gizzard of earthworms is definitely of endodermal origin. Contrary to the opinion that tissue of endodermal origin is unable to synthesize chitin, the gizzard epithelium secretes large amounts of chitin-containing material which has special properties. 28.7 +/- 5.7% of the dry weight proved to be chitin; the microfibres form a random felt-like texture. They are not arranged in layers comparable to those found in arthropod cuticle. The protein content amounts to 44.9 +/- 7.1% of the dry weight; the remaining material contains at least uronic acids. In the protein matrix large amounts of the enzymes amylase and protease have been demonstrated. As the so-called cuticle is sloughed off at the lumen side, these enzymes are mingled with the gut contents. It might be called a gastric shield, as it closely resembles this structure, widespread among Mollusca. The thickness of the gizzard cuticle varies between 10 and 90 mum in Lumbricus terrestris and 10-50 mum in L. rubellus. Autoradiography has shown that it is replaced at a high rate. In Lumbricus terrestris it is renewed completely in less than 60 hr, and in smaller Lumbricus rubellus, this takes place in about 48 hr. These results are in agreement with the biochemical findings.     

Impact of chemical manipulation of tarsal liquids on attachment in the Colorado potato beetle, Leptinotarsa decemlineata

Insect tarsal attachment forces are thought to be influenced by the viscosity and surface tension of a thin film of adhesive liquid (wet adhesion). In beetles, this fluid has been shown to be composed mainly of lipophilic substances that are similar to the cuticular lipids. In this study we investigate whether and how the chemical composition of footprint lipids affects attachment forces in the Colorado potato beetle, Leptinotarsa decemlineata. After application of standardised mixtures of synthetic n-alkanes or alkenes, or a concentrated hydrocarbon extract to the surface of the elytra, we tested the beetles’ attachment performance using a beam force transducer. The results show that only the unsaturated components, but not the straight-chained alkanes reduced friction forces, confirming that attachment performance is influenced by the chemical composition of the adhesive secretion. We estimated the volume of footprint droplets and calculated a mean thickness of the liquid layer of 0.04 μm. The measured friction exceeded the viscous and capillary force expected for a film of this thickness. Therefore, alternative mechanisms (i.e. shear-thinning and solid-like behaviour) for the generation of attachment forces and their dependence on the chemical composition of the liquid are discussed.     

Small peptides,a life-long store of amino acid in adult Drosophila and Calliphora

A sizable component of small peptide is probably an important store of amino acid in Calliphora and Drosophila. Quantitative amino acid analysis of the peptides in adult male Calliphora erythrocephala and Drosophila subobscura show that their composition is very similar. It is shown in Calliphora that the amount of peptide present in adults varies with age and feeding regime. Further, the peptide composition of the haemolymph indicates that the peptides are stored intracellularly. However, there is evidence which suggests that their hydrolysis takes place in the haemolymph, thus providing the whole fly with free amino acid and the haemolymph with osmotic stability.     

Direct Binding of a Plant LysM Receptor-like Kinase, LysM RLK1/CERK1, to Chitin in Vitro

Plants induce immune responses against fungal pathogens by recognition of chitin, which is a component of the fungal cell wall. Recent studies have revealed that LysM receptor-like kinase 1/chitin elicitor receptor kinase 1 (LysM RLK1/CERK1) is a critical component for the immune responses to chitin in Arabidopsis thaliana. However, the molecular mechanism of the chitin recognition by LysM RLK1 still remains unknown. Here, we present the first evidence for direct binding of LysM RLK1 to chitin. We expressed LysM RLK1 fused with yeast-enhanced green fluorescent protein (LysM RLK1-yEGFP) in yeast cells. Binding studies using the solubilized LysM RLK1-yEGFP and several insoluble polysaccharides having similar structures showed that LysM RLK1-yEGFP specifically binds to chitin. Subsequently, the fluorescence microscopic observation of the solubilized LysM RLK1-yEGFP binding to chitin beads revealed that the binding was saturable and had a high affinity, with a K_d of ∼82 nm. This binding was competed by the addition of soluble glycol chitin or high concentration of chitin oligosaccharides having 4–8 residues of N-acetyl glucosamine. However, the competition of these chitin oligosaccharides is weaker than that of glycol chitin. These data suggest that LysM RLK1 has a higher affinity for chitin having a longer residue of N-acetyl glucosamine. We also found that LysM RLK1-yEGFP was autophosphorylated in vitro and that chitin does not affect the phosphorylation of LysM RLK1-yEGFP. Our results provide a new dimension to chitin elicitor perception in plants.     

Specificity and Affinity of Lac Repressor for the Auxiliary Operators O2 and O3 Are Explained by the Structures of Their Protein-DNA Complexes

The structures of a dimeric mutant of the Lac repressor DNA-binding domain complexed with the auxiliary operators O2 and O3 have been determined using NMR spectroscopy and compared to the structures of the previously determined Lac-O1 and Lac-nonoperator complexes. Structural analysis of the Lac-O1 and Lac-O2 complexes shows highly similar structures with very similar numbers of specific and nonspecific contacts, in agreement with similar affinities for these two operators. The left monomer of the Lac repressor in the Lac-O3 complex retains most of these specific contacts. However, in the right half-site of the O3 operator, there is a significant loss of protein-DNA contacts, explaining the low affinity of the Lac repressor for the O3 operator. The binding mode in the right half-site resembles that of the nonspecific complex. In contrast to the Lac-nonoperator DNA complex where no hinge helices are formed, the stability of the hinge helices in the weak Lac-O3 complex is the same as in the Lac-O1 and Lac-O2 complexes, as judged from the results of hydrogen/deuterium experiments.     

Analysis of samples of Hipparion(Mammalia,Perissodactyla) from the Concud localities,Turolian of Spain

Samples, mainly of isolated teeth, of Hipparion concudensePirlot from the Turolian fossil sites “Concud”. Cerro de la Garita, Barranco de las Calaveras, Concud III, Masia del Barbo, and Los Mansuetos, all in the Calatayud-Teruel area, Spain, are analysed and compared. The teeth from “Concud”, Cerro, and Masia are similar and larger than those from Barranco, Concud III, and Los Mansuetos, which between them are similar. A possible trend towards decrease in size is indicated. The stratigraphic position of these sites is briefly discussed.     

Cassane diterpenoids from the stem of Caesalpinia pulcherrima

Cassane diterpenoids: pulcherrin A, pulcherrin B, pulcherrin C, neocaesalpin P, neocaesalpin Q and neocaesalpin R, together with eight known compounds: isovouacapenol C, 6β-cinnamoyl-7β-hydroxy-vouacapen-5α-ol, pulcherrimin E, pulcherrimin C, α-cadinol, 7-hydroxycadalene, teucladiol and bonducellin were isolated from the stem of Caesalpinia pulcherrima. The chemical structures were elucidated by analysis of their spectroscopic data.     

Action of chitinase on spines of the diatom Thalassiosira fluviatilis

An electron microscopic study of the degradation of the chitin spines of the diatom Thalassiosira fluviatilis by Streptomyces chitinase revealed that only the apices of fibrils are broken down. The result suggests that the enzymolysis of crystalline chitinous structures may be rate-limited by the area of microfibril apices available, which varies with chitin source. A suspension of spines can be used as an assay for chitinase activity by monitoring the rate of loss of turbidity, and although this is not a sensitive assay, it does allow assessment of activity on a crystalline substrate.     

Expression profiling of the triterpene saponin biosynthesis genes FPS, SS, SE, and DS in the medicinal plant Panax notoginseng

Panax notoginseng (Burk) F. H. Chen, an economically significant medicinal plant with hemostatic and health tonic activities, has been used in Traditional Chinese Medicine (TCM) for more than 3000 years. Triterpene saponins are responsible for most of the pharmacological activities of P. notoginseng. Here, we cloned five cDNA sequences encoding the key enzymes involved in triterpene saponin biosynthesis, namely, PnFPS, PnSS, PnSE1, PnSE2, and PnDS, and analyzed the conserved domains and phylogenetics of their corresponding proteins. Their organ-specific expression patterns in four-year-old P. notoginseng were detected by real-time PCR, showing that they were all most highly expressed in flowers. In addition, four of the genes, excluding PnSE2, were upregulated in leaves following stimulation with methyl jasmonate. This study is the first comprehensive analysis of the expression patterns of pivotal genes for triterpene saponin biosynthesis in P. notoginseng and provides a basis to further elucidate the molecular mechanism for the biosynthesis of these medically important compounds.     

Serratia marcescens chitinase: One-step purification and use for the determination of chitin

The extracellular chitinase produced by Serratia marcescens was obtained in highly purified form by adsorption-digestion on chitin. After gel electrophoresis in a nondenaturing system, the purified preparation exhibited two major protein bands that coincided with enzymatic activity. A study of the enzyme properties showed its suitability for the analysis of chitin. Thus, the chitinase exhibited excellent stability, a wide pH optimum, and linear kinetics over a much greater range than similar enzymes from other sources. The major product of chitin hydrolysis was chitobiose, which was slowly converted into free N-acetylglucosamine by traces of β-N-acetylglucosaminidase present in the purified preparation. The preparation was free from other polysaccharide hydrolases. Experiments with radiolabeled yeast cell walls showed that the chitinase was able to degrade wall chitin completely and specifically.     

Mixtecacin,a prenylated flavanone and oaxacacin its chalcone from the roots of Tephrosia woodii

From the roots of Tephrosia woodii, a new Mexican Tephrosia species, a new prenylated flavanone, oaxacacin, and its chalcone, mixtecacin, have been isolated and their structures elucidated from their chemical properties and spectral data.