Effects of food deprivation on Latrodectus hasselti Thorell (Araneae: Theridiidae), the Australian redback spider

Abstract

Food deprivation tests indicate that most sub-adult and adult female Latrodectus hasselti spiders would be able to endure long periods of starvation if incarcerated in cargo. The data show that, under appropriate conditions, sub-adults survive for up to 160 days and some adults for more that 300 days. Temperature is an important variable with longevity being greatest at 10°C and markedly reduced at 25°C. Sluggishness is more pronounced at lower temperatures and probably reflects reduced metabolic rates. Even after 2–3 months without food, most spiders recover when fed.

Five stages mark the progress of starvation (Indices of Starvation) and reflect a gradual decline in the spider’s normal functions. As the abdomen shrinks, with a concomitant loss of hydraulic pressure, there is a gradual decline in web-building and locomotory activities which ultimately end in the spider’s death. It is assumed that nutritional deficiency and, to a lesser extent, dehydration contribute to mortality.     

Possible pathogens of social wasps (Hymenoptera: Vespidae) and their potential as biological control agents

Abstract

Boutin et al. (2006) claimed that American and Eurasian red squirrels use an unknown environmental cue to anticipate the availability of the abundant food of an autumn seed mast, and produce more young than usual in the previous spring and summer. But these small mammals need increased supplies of protein to produce and support young, therefore they must have had access to some other protein‐rich food that was available before the mast was ripe. There are other small mammalian seed‐eaters that increase their reproductive output ahead of the maturation of a seed mast. It seems likely that, in each case, females are able to produce extra young in advance because they eat the amino acid‐rich inflorescences and unripe seeds of the mast and/or larval insects that also increase their numbers in the spring of a mast year by eating the same enriched plant food.     

Engineering the bilayer: Emerging genetic tool kits for mechanistic lipid biology

The structural diversity of lipids underpins the biophysical properties of cellular membranes, which vary across all scales of biological organization. Because lipid composition results from complex metabolic and transport pathways, its experimental control has been a major goal of mechanistic membrane biology. Here, we argue that in the wake of synthetic biology, similar metabolic engineering strategies can be applied to control the composition, physicochemical properties, and function of cell membranes. In one emerging area, titratable expression platforms allow for specific and genome-wide alterations in lipid biosynthetic genes, providing analog control over lipidome stoichiometry in membranes. Simultaneously, heterologous expression of biosynthetic genes and pathways has allowed for gain-of-function experiments with diverse lipids in non-native systems. Finally, we highlight future directions for tool development, including recently discovered lipid transport pathways to intracellular lipid pools. Further tool development providing synthetic control of membrane properties can allow biologists to untangle membrane lipid structure-associated functions.     

Potential applications of natural origin polymer-based systems in soft tissue regeneration

Despite the many advances in tissue engineering approaches, scientists still face significant challenges in trying to repair and replace soft tissues. Nature-inspired routes involving the creation of polymer-based systems of natural origins constitute an interesting alternative route to produce novel materials. The interest in these materials comes from the possibility of constructing multi-component systems that can be manipulated by composition allowing one to mimic the tissue environment required for the cellular regeneration of soft tissues. For this purpose, factors such as the design, choice, and compatibility of the polymers are considered to be key factors for successful strategies in soft tissue regeneration. More recently, polysaccharide-protein based systems have being increasingly studied and proposed for the treatment of soft tissues. The characteristics, properties, and compatibility of the resulting materials investigated in the last 10 years, as well as commercially available matrices or those currently under investigation are the subject matter of this review.     

Chemically-Synthesized Gene Encoding Modified Human Superoxpde Dismutase: Its Construction,Expression and Properties of the Product

The gene encoding modified human superoxide dismutax (h-SOD) with 153 amino acid residues was constructed by chemical synthesis using the phosphoramidite method. The gene was designed so as to use bacterial codons for expression in prokaryotes and to introduce several unique restriction sites for further mutagenesis by the cassette exchange method. The distance between Shine-Dalgarno sequence and initiation codon was adjusted to maximum expression by using synthesized oligonucleotide. In addition, Cys 6 of h-SOD was changed to Ala to improve instability of native h-SOD.

Synthesized structural gene of h-SOD was expressed in E. coli after induction of isopropyl β-D-thiogalactoside by inserting the gene into the expression vector pKK223–3 having tac promoter. The gene that has 10 base pairs between Shine-Dalgarno sequence and initiation codøn showed the most efficient expression. The gene produced three active SOD isomers as revealed by chromatofocusing.

The main isomer was purified to homogeneity and characterized. The h-SOD-Ala⁶ showed similar properties to those of native h-SOD with respect to molecular weight, subunit structure, absorption spectrum. but the modified SOD was more resistant to heat denaturation than was native h-SOD; half-denaturing temperature was shifted by 10°C. Thus. the exchange of Cys 6 to Ala of h-SOD increased a stability of the enzyme.     

Relative availability and utilization of algae in two subarctic rivers

The ash free dry weight of algae in the plankton, epilithon and gut of predominant herbivores was determined between June 1975 and July 1976 in 2 subarctic Canadian rivers (Baker Creek, Yellowknife River). Algae usually represented < 1% of suspended solids in both rivers and up to 8o% of material attached to rocks. While they were never found in the gut of rotifers and copepod nauplii in Baker Creek, they accounted for 0.5% of the contents of the planktonic conchostracon Lynceus brachyurus. Due to the inpalatable colonial structure of most attached algal species, the zoobenthos (mainly mayfly nymphs) contained only a few cells. Size selection against large fragments of detritus resulted in increased consumption of algae (5–13%) by Simulium venustum, S. decorum and S. arcticum. In the Yellowknife River, Diaptomus ashlandi (CIII–CVI stages) and Holopedium gibberum contained only a few (30–50) algal cells during summer. Because of size selection, large algae were not ingested by these species. The inpalatability of colonial algae greatly reduced consumption in the predominant zoobenthic species, Ephemerella coxalis and E. margarita. While all species digested diatoms, the Chlorophyta usually passed through the gut unharmed. It is concluded that algae are not an important energy source for invertebrates in either stream.     

Dissociation and reconstitution of bovine seminal RNAase: Construction of a hyperactive hybrid dimer

The quaternary structure of bovine seminal ribonuclease, the only dimeric protein in the superfamily of ribonucleases, is maintained both by noncovalent forces and by two intersubunit disulfides. The available monomeric derivatives of the enzyme may not be reassembled into dimers. They are catalytically active, but do not retain certain properties of the dimeric enzyme, such as: (i) the ability to respond cooperatively to increasing substrate concentrations in the rate-limiting reaction step; and (ii) the antitumor and immunosuppressive actions. In this report we describe the preparation of stable monomers of seminal ribonuclease which can be reassociated into covalent dimers indistinguishable from the native protein. With this procedure a hybrid dimer was constructed, made up of a native subunit associated to a subunit catalytically inactivated by selective alkylation of the active site His-119. This dimer was found to have enzymic properties typical of monomeric ribonucleases, such as a hyperbolic saturation curve in the hydrolytic rate-limiting step of the reaction. However, the hybrid dimer was one order-of-magnitude more active than the dimeric enzyme.