The structure of aleuriaxanthin

The structure of aleuriaxanthin ex. Aleuria aurantia has been shown to be 1′,2′-dihydro-1′,16′-didehydro-β,ψ-caroten-2′-ol (V) by means of chemical and spectroscopic evidence.     

Senna barnebyana (Leguminosae: Caesalpinioideae), a new “Cassia” from Peru

Cassia aurantia Benth. sensu auct. is not the species to which Bentham referred, but is an undescribed entity herein namedSenna barnebyana.     

A unique enzyme of acetic acid bacteria, PQQ-dependent alcohol dehydrogenase, is also present in Frateuria aurantia

A membrane-bound, pyrroloquinoline quinone (PQQ)-dependent alcohol dehydrogenase (ADH) was purified from Frateuria aurantia LMG 1558^T. Although F. aurantia belongs to a group of γ-Proteobacteria, the characteristics of its PQQ-ADH were similar to the enzyme characteristics of the typical high-acetic acid-resistant bacterium Gluconacetobacter europaeus from the group of α-Proteobacteria. The PQQ-dependent ADH was solubilized from the membranes and purified after anionic, cationic, and affinity chromatography with specific activity of 117 U/mg. The purified enzyme was estimated to be composed of two subunits of ca. 72 and 45 kDa, as judged by SDS-polyacrylamide gel electrophoresis. The purified enzyme had maximum activity at pH 4.5 and showed the highest substrate specificity to ethanol, isoamyl alcohol, 1-butanol, and 1-propanol. The deduced sequences of cloned genes adhA and adhB encoding subunits I and II of PQQ-ADH showed 80 % amino acid (AA) identity to AdhA and 68 % AA identity to AdhB of Ga. europaeus V3 (LMG 18494). Because of the high similarity between genes encoding subunits I and II of PQQ-ADH and its homologous genes found in a distantly related taxonomic group of acetic acid bacteria, the results suggest the possibility of horizontal gene transfer between these two groups of genera.     

The intracellular polyglucose storage granules of Spirochaeta aurantia

Extracts of Spirochaeta aurantia contained granules approximately 36 nm in diameter. These granules were purified by isopycnic centrifugation on CsCl gradients and shown on the basis of chemical and spectroscopic evidence to be glycogen. Electron microscopic cytochemical methods revealed glycogen-like granules in S. aurantia cells.     

Revision of the genus Ficiana Ghauri and its relationship to other genera in Empoascini (Hemiptera,Cicadellidae, Typhlocybinae)

The empoascine genus Ficiana Ghauri is reviewed based on specimens from China. One new Ficiana species, Ficiana aurantia sp. n. is described from Guangxi in south China. An identification key to all species in this genus is provided. The morphological characters of Ficiana and related genera in this tribe are discussed.     

Water extraction by the major ampullate duct during silk formation in the spider, Argiope aurantia Lucas

The water, K⁺ and Na⁺ content of naturally produced major ampullate silk as well as silk mechanically drawn from the spider Argiope aurantia have been compared to that of the major ampullate gland. It is demonstrated that water is extracted by the major ampullate duct and that this process is accompanied by an exchange of K⁺ for Na⁺. The significance of these observations is discussed.     

A shift in microvillus membrane fucosylation to sialylation by ethanol ingestion in rat intestine

The luminal surface of enterocytes is covered with glycocalyx which is rich in glycoproteins. Ethanol ingestion is shown to induce morphological and biochemical changes in the intestine. In this study, the effect of ethanol ingestion on membrane glycoproteins has been investigated. Chemical analysis of microvillus membranes revealed an increase in hexose and sialic acid contents, but a reduction in fucose levels in ethanol-fed rats compared with controls. The observed changes were apparent in animals fed with ethanol for 35–56 days compared with controls. Lectin-binding assay indicated an increase in Wheat germ agglutinin (affinity for GlcNAc/sialic acid) and a decrease in Aleuria aurantia (affinity for α-l-fucose) reactivity of brush borders in ethanol-fed animals for 4–8 weeks. Western blot analysis using biotin-labeled Wheat germ agglutinin revealed increased binding to proteins of M_r 66–205 kDa in ethanol-fed rats compared with controls. The binding of Aleuria aurantia to membrane proteins of M_r 97–185 kDa was reduced in ethanol-fed animals. These findings suggest that long-term ethanol feeding modulates the sialylation and fucosylation processes of microvillus membrane proteins in rat intestine. This could affect the intestinal digestive and absorptive functions in chronic alcoholism.     

Feeding ecology of the orb-weaving spiderArgiope aurantia [Araneae: Araneidae] in a cotton agroecosystem

Twenty females of the orb-weaving spiderArgiope aurantia Lucas were introduced into a cotton field in east Texas in order to study the feeding ecology of this spider. In the 24 h after the release of these spiders in the cotton field, one had moved over a distance of 53 m. The released spiders spun webs with an average diameter of 33.5 cm with the hub an average of 39 cm above the ground. The diet ofA. aurantia was diverse which characterizes this species as a food generalist. Major food components were aphids (30%), Diptera (26.8%), grasshoppers (17.9%), and Hymenoptera (12.6%). The spiders' prey length ranged from 0.4 to 47 mm (mean =7.7±0.83 mm). Adult females ofA. aurantia have the potential to kill prey of up to ca. 200% of their own size. However, two-thirds of the prey items had a length of <3 mm, while only 25% of the prey items had a length of ≥20 mm.A. aurantia was found to be a predator of the cotton fleahopper (about 1% of the spiders' diet), which is a key pest of cotton.      

Phylogenetic analysis and evolutionary studies of plant carotenoid cleavage dioxygenase gene

The oxidative breakdown of carotenoid evidences the formation of apocarotenoids through carotenoid cleavage dioxygenases (CCDs). Numerous CCDs and apocarotenoids have been identified and characterized in plants. Using available sequence data, a study was performed to investigate the phylogenetic relationship among CCD genes and to statistically estimate the sequence conservation and functional divergence. In total, 77 genes were identified from 39 species belonging to 21 families. Our result of phylogenetic analysis indicated the existence of well-conserved subfamilies. Moreover, comparative genomic analysis showed that the gene structures of the CCDs were highly conserved across some different lineage species. Through functional divergence analysis, a substantial divergence was found between CCD subfamilies. In addition, examination of the site-specific profile revealed the critical amino acid residues accounting for functional divergence. This study mainly focused on the evolution of CCD genes and their functional divergence which may deliver an initial step for further experimental verifications.     

Carotenoids found in Littorina littorea and their relationship to parasitic infection by larva trematodes

Littorina littorea from Long Island Sound feed primarily on algae: Chlorophyceae (three species) and Rhodophyceae (two species). Carotenoids from the algae accumulate in tissues of the snail in either an unchanged or a metabolized state. β-Carotene, the major pigment of green and red algae, was isolated from the foot, hepatopancreas, and nephridium of these snails. Six oxygenated carotenoids, not completely identified, were isolated from the same tissues. The snails show a variation in foot color from white to brown to red. L. littorea is parasitized by trematode larvae of Cryptocotyle lingua and Cercaria parvicaudata from which β-carotene and one oxygenated carotenoid were isolated. Contrary to previous work, there is no relation between foot color of the snail and parasitic infection. Neither age nor sex appears to have any relation to foot color. Although carotenoid pigments are known to cause the variation in foot color, the reasons or factors for their accumulation in the snail tissue have not been established. Some hypothetical explanations are discussed.     

Absolute configuration of eschscholtzxanthin

The chirality of eschscholtzxanthin (all-trans (3S,3′S)-4′,5′-didehydro-4,5′-retro-β,βcarotene-3,3′-diol) at 3,3′ was assigned from the CD correlation of the natural material and the semi-synthetic carotenoid prepared by (NBS-dehydrogenation of natural zeaxanthin ((3R,3′R)-β,β-carotene-3,3′-diol). The δ^6(6′)-trans configuration followed from ¹H NMR evidence, including nuclear Overhauser experiments with rhodoxanthin, retrodehydro-carotene (4′,5′-didehydro-4,5′-retro-β,β-carotene) and smaller retro model compounds revealing a general preference for the δ⁶-trans configuration in retro compounds. Biosynthetic considerations are made.     

Cloning and expression of a functional fucose-specific lectin from an orange peel mushroom, Aleuria aurantia

Aleuria aurantia lectin (AAL) shows sugar-binding specificity for L-fucose. A λgt11 expression library was constructed from A. aurantia poly(A) RNA and screened with a polyclonal antiserum directed against AAL. An immunopositive clone carrying 1.3-kb EcoRI fragment was obtained. The fragment encoded AAL, but lacked a nucleotide sequence corresponding to the two amino-terminal amino acids. The 5′-terminal part of the fragment was replaced with a chemically synthesized DNA fragment and inserted into an expression vector to yield a plasmid pKA-1. Escherichia coli carrying pKA-1 expressed functional AAL and the recombinant AAL showed the same immunological properties as those of natural AAL.     

The role of spider cocoons in controlling desiccation

Summary The abilities of the cocoons of the spiders Mecynogea lemniscata and Argiope aurantia to protect the enclosed egg and spiderling stages from desiccation were investigated in the laboratory under controlled humidities, and in the field under ambient conditions. For M. lemniscata, which has a relatively small clutch (8–30 eggs) and remains in the cocoon for approximately 9–10 months, removal of the cocoon had no effect on water loss from the egg stage, nor did it adversely affect hatching or molting success. Cocoon removal did, however, significantly affect water loss and, consequently, survival in the spiderling stage at all humidities in the laboratory and in the field. The importance of the cocoon for survival is probably related to the unusually long time M. lemniscata spiderlings spend in the cocoon overwintering. For A. aurantia, which has a substantially larger clutch size (300–1400 eggs) and remains in the cocoon for a shorter 6–7 months, cocoon removal had no effect on water loss, egg hatching success, molting success, nor spiderling survival. The lack of an effect suggests that other factors (e.g., relative humidity at the oviposition site, or a large clutch size) may be more important in controlling water loss for A. aurantia.     

Linking properties of an orb‐weaving spider's capture thread glycoprotein adhesive and flagelliform fiber components to prey retention time

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Lactucaxanthin,an ε,ε-carotene-3,3′-diol from Lactuca sativa

Chemical and spectroscopic evidence including ¹H NMR and CD is presented, demonstrating the (3R,6R,3′R,6′R)-ε,ε-carotene-3,3′-diol structure of a new carotenoid, lactucaxanthin. Lactucaxanthin, isolated from Lactuca sativa, is the sixth chiral isomer encountered in nature ofthe ten possible chiral isomers of ε,ε-carotene-3,3?diol. In achemosystematic screening,lactucaxanthin was restricted to Lactuca and a few closely related genera within the tribe Cichorieae of the Compositae.     

Chemotaxis in Borrelia burgdorferi

Borrelia burgdorferi is a motile spirochete which has been identified as the causative microorganism in Lyme disease. The physiological functions which govern the motility of this organism have not been elucidated. In this study, we found that motility of B. burgdorferi required an environment similar to interstitial fluid (e.g., pH 7.6 and 0.15 M NaCl). Several methods were used to detect and measure chemotaxis of B. burgdorferi. A number of chemical compounds and mixtures were surveyed for the ability to induce positive and negative chemotaxis of B. burgdorferi. Rabbit serum was found to be an attractant for B. burgdorferi, while ethanol and butanol were found to be repellents. Unlike some free-living spirochetes (e.g., Spirochaeta aurantia), B. burgdorferi did not exhibit any observable chemotaxis to common sugars or amino acids. A method was developed to produce spirochete cells with a self-entangled end. These cells enabled us to study the rotation of a single flagellar bundle in response to chemoattractants or repellents. The study shows that the frequency and duration for pausing of flagella are important for chemotaxis of B. burgdorferi.     

ERRATA

June Number: p. 276, last line, for 9–16 read 9–12. p. 279, l. 16, for Pterocera amantia read Pterocera aurantia.      

CD36 homolog divergence is responsible for the selectivity of carotenoid species migration to the silk gland of the silkworm Bombyx mori

Dietary carotenoids are absorbed in the intestine and delivered to various tissues by circulating lipoproteins; however, the mechanism underlying selective delivery of different carotenoid species to individual tissues remains elusive. The products of the Yellow cocoon (C) gene and the Flesh (F) gene of the silkworm Bombyx mori determine the selectivity for transport of lutein and β-carotene, respectively, to the silk gland. We previously showed that the C gene encodes Cameo2, a CD36 family member, which is thought to function as a transmembrane lipoprotein receptor. Here, we elucidated the molecular identity of the F gene product by positional cloning, as SCRB15, a paralog of Cameo2 with 26% amino acid identity. In the F mutant, SCRB15 mRNA structure was severely disrupted, due to a 1.4 kb genomic insertion in a coding exon. Transgenic expression of SCRB15 in the middle silk gland using the binary GAL4-UAS expression system enhanced selective β-carotene uptake by the middle silk gland, while transgenic expression of Cameo2 enhanced selective lutein uptake under the same GAL4 driver. Our findings indicate that divergence of genes in the CD36 family determines the selectivity of carotenoid species uptake by silk gland tissue and that CD36-homologous proteins can discriminate among carotenoid species.