Structure and properties of pectin gels in plant cell walls

Abstract This review deals with recent advances in the structural characterization of pectins and the gels which they form, in relation to auxin-induced extension growth, the ripening of fruit, and cellular recognition. Pectins are block polysaccharides. Heavily branched, largely methyl-esterified blocks alternate with unbranched blocks of varying degrees of esterification. The unbranched, non-esterified blocks can aggregate through calcium binding to form the junction zones that hold a gel together. The aggregates are of two, or possibly four, chains at low calcium levels, and larger with excess calcium. The fall in wall pH during auxin-induced growth activates glycanase enzymes. These may attack some components of the pectic fraction, as well as xyloglucans. Pectin-bound calcium ions may be displaced but this probably has little effect on gel strength. Pectins may be cross-linked by diferulate esters when growth stops. The softening of ripe fruit is due to loss of cohesion in the pectin gel. In apples this results from replacement of the pectins by more esterified forms. In many other fruits it results from depolymerization by polygalacturonases, assisted by pectinesterases, so that the remaining segments are too short for effective calcium binding. Pectins have a further role in the recognition reactions between plant cells and some of their bacterial and fungal pathogens.     

The Possible Involvement of Cyclic AMP and Volatile Substance (s) in the Development of a Macrocyst-Forming Strain of Dictyostelium mucoroides

A mutant MF1 previously isolated from Dictyostelium mucoroides -7 (Dm7) formed macrocysts with or without light when plated on agar at high cell dinsities. At lower cell densities, however, the MF1 cells formed only fruiting bodies. This failure to form macrocysts was shown to be due to the subthreshfold concentration of a volatile substance(s) required for macrocyst formation. Although ammonia is a volatile substance produced by both the Dm7 and MF1 cells, no evidence of its involvement in macrocyst formation was obtained. Mixing the Dm7 and MF1 in a one-to-one ratio resulted only in fruiting body formation suggesting that the Dm7 cells produced a factor which allowed MF1 cells to form fruiting bodies. This factor may be cyclic AMP (cAMP) since addition of cAMP to the medium directed development of MF1 cells to fruiting body formation. The effect of cAMP was exhibited most conspicuously when MF1 cells were exposed at the aggregation stage. Based on these results it is suggested that developmental pathway of the D. mucoroides macrocystforming strain Dm7 and its mutant MF1 may be determined by the relative concentrations of the volatile, macrocyst-inducing substance(s) and cAMP at the aggregation stage.     

Algal borings and framboidal pyrite in Upper Ordovician brachiopods

Algal borings in the shells of the articulate brachiopods Plaesiomys subquadrata (Hall) and Hebertella sinuata (Hall) from the Richmond Formation of Ohio are empty, or partially to entirely filled with pyrite. The pyrite occurs as single framboids and other crystal forms, or in chains filling the bores. The borings provide some insight into the early diagenetic history of the Richmond sediments near Cincinnati. Pyritization probably occurred within a few years, only a short distance (a few centimeters) below the sediment surface through the activities of sulfur-reducing bacteria. Pyrite precipitated around a nucleus such as a bacterium or algal cell, or developed within an organic structure such as an algal cell or organic membrane.     

Why change mates?

In some wading birds (Charadrii) each adult rears a brood alone. The female leaves her first clutch with her first mate before herself rearing a clutch fertilized by a second male, who is already tending its first mate's first clutch. We here develop a simple model to account for the exchange of mates between clutches, and relate it to reported field studies. We suggest that females are attempting to be polygamous, rather than simply bigamous. Provided a female has a chance of obtaining a second, unmated male and that the costs of leaving the first male before remating are not high, matechanging will be favoured over monogamy. The implications of this model to the evolution of the more usual forms of polyandry and of male-like females are discussed.     

Distribution of Fibronectin and Collagen during Mouse Limb and Palate Development

Indirect immunofluorescence has been used to study the distribution of fibronectin and collagen types I, II, and III in the developing primary and secondary palatal processes and forelimb buds of the Swiss Webster (NIH) mouse. In the palatal processes fibronectin and types I and III collagen are distributed throughout the mesenchyme. Fibronectin is present in the basement membrane, while types I and III collagen are localized in a linear, discontinuous fashion beneath the basement membrane. Fibronectin is not observed in the epithelium, including the presumptive fusion areas. In the forelimb bud these components show a similar distribution prior to chondrogenesis (early day 11). When chondrogenesis commences (late day 11 or early day 12) fibronectin and, to a lesser degree, types I and III collagen are apparently concentrated in the core mesenchyme, suggesting that fibronectin has a role in initiating chondrogenesis, perhaps by increasing cellular aggregation. Type II collagen is observed only in chondrogenic regions. The codistribution of fibronectin and types I and III collagen supports in vitro studies which indicate that cells use fibronectin to bind to collagen in the matrix. The developing chondrogenic regions appear to lose fibronectin gradually, concomitant with the appearance of type II collagen, suggesting that fibronectin is not involved in the maintenance of functional chondrocytes in their matrices.     

Ribulose-1,5-Diphosphate Carboxylase Protein during Flag Leaf Senescence

Ribulose-l,5-diphosphate (RuDP) carboxylase protein and activitywere determined in relation to net photosynthetic rate duringthe senescence of intact flag leaves of wheat on the plant.Initially the decrease in RuDP carboxylase activity was greaterthan the decline in net photosynthesis. The major decrease inRuDP carboxylase activity over this period resulted from a decreasein enzyme specific activity from 11 to 2 µmol CO₂ fixedh^–1 mg^–1 protein. Loss of RuDP carboxylase proteindid not occur until late in senescence by which time chlorophyllconcentration had decreased by more than 50%. Treatment of flagleaves at weekly intervals with either 1000 parts 10^–62-chloro-ethyltrimethylammonium chloride or 100 parts 10^–6gibberellic acid with 1 part 10^–6 kinetin did not significantlyaffect net photosynthetic rate, RuDP carboxylase protein oractivity during senescence.     

Ribulose 1, 5-Bisphosphate Carboxylase/Oxygenase Activity and Photorespiration during the Ageing of Flag Leaves of Wheat

Photosynthesis, photorespiration, and ribulose bisphosphatecarboxylase/oxygenase activities were measured in intact flagleaves of wheat during ageing. Photorespiration declined verylittle as the leaves aged, and much less than photosynthesis.These changes could not be explained by changes in the ribulosebisphosphate carboxylase to oxygenase ratio of fraction 1 protein.As the leaves grew older the enzyme activities in extracts ofleaves declined in parallel so the ratio remained constant.     

Thermoregulation in orb-web spiders: new descriptions of thermoregulatory postures and experiments on the effects of posture and coloration

Ideally, diurnal orb-web spiders should be able to ignore problems of insolation when siting their webs and should be able to operate such webs without the necessity of retiring into shade. Postures that minimize the surface area of the spider exposed to insolation may help to free the spider from the danger of overheating. Such postures are here described for the first time for Argiope argentata and three species of Gasteracantha . Experiments with dead Nephila clavipes show that postures described as thermoregulatory do, in fact, reduce absolute temperatures (and the rate of temperature increase) compared to normal predatory postures.
Metalic or other reflectant coloration occurs in many species of diurnal orb-web spiders. These are partly listed herein. Experiments with one such species, Argiope argentata , show that overpainting the silver parts increases both the rate of temperature increase and the absolute temperatures reached when naturally coloured and black-painted spiders are exposed to the same radiant heat sources.
It is suggested that these results on the probable thermoregulatory function of metallic coloration can provide insights into the probable habitat distributions of species whose coloration is known but whose ecology is presently unknown. The general question of adaptive coloration in spiders is discussed in the light of these results.     

Translocation and Metabolism of Leaf Applied Hexachlorophene in Peanuts

Translocation, distribution, metabolism and photolysis of hexachlorophene (HCP) were investigated in peanut plants (Arachis hypogea L., Spanish type) grown under standardized conditions and treated with ^l4C-ring-labeled HCP. Treatment time ranged from 0–114 days. Autoradiographic analyses were performed on all plants. Selected plant tissues were extracted and chromatographed, using both thin layer and gas liquid chromatography. No translocation of HCP was detected in the plant tissue. No HCP metabolites were found. Some HCP was lost from the leaves and inert controls at a specific rate per unit time. The rates were slightly different, being slower on the leaves than on the controls. At the end of the 114-day treatment and based on regression analysis of thin layer chromatographic plates, an average of 68% of the applied HCP remained unaltered on the treated plants and an average of 77% remained on the controls. This indicated that, respectively, 32 and 23% of the original HCP had been altered. This 9% difference was statistically significant. Upon further analyses of the above data, using gas chromatographic methods, as many as 14 peaks were found in the treated samples and the controls, including some parent material. Ultraviolet photolysis seems to be the mechanism responsible for alteration of the HCP on the treated plants and controls. Two photolysis products have been identified by gas liquid chromatography-mass spectral analysis. Twelve other electrophylic compounds have been found in various treated plant or control extracts. Further analyses will be necessary to verify the identification and quantification of the other degradation products.