The Relationship between Structure and Activity of Taurolin

Taurolin [Bis(1,1-dioxo-perhydro-1,2,4 thiadiazinyl-4)methane] is an antimicrobial compound formed by the condensation of two molecules of taurine with three of formaldehyde. It has been suggested that it releases formaldehyde in contact with bacteria. Evidence from TLC, HPLC and NMR spectroscopy indicates that taurolin is mostly hydrolysed in aqueous solution to release one molecule of formaldehyde and two monomeric molecules (1,1-dioxo-perhydro-1,2,4-thiadiazine and its carbinolamine derivative). A stable equilibrium is established. Antibacterial activity is not entirely due to adsorption of free formaldehyde but also to reaction with a masked (or latent) formaldehyde, as the activity of taurolin is greater than formaldehyde. The monomer is only slightly active by comparison.     

Hormone-Stimulated Iipid Synthesis in Mammary Culture

Mammary explants from midpregnant mice were cultured for upto 96 hr with various combinations of insulin, prolactin, andcorticosterone. Labeled glucose was added to cultures at 4 hrprior to termination, and explant morphology, glucose uptake,and lipid synthesis were studied in hormone-free and hormone-containingmedia. The results show that without hormones, explants takeup glucose and synthesize lipid at minimal rates. After 48 hrthese activities appear to be primarily those of adipose tissuesince epithelial and connective tissue degenerate without hormones. Insulin increases cell number for 24 hr and maintains survivalfor 96 hr. Its stimulatory effect on lipogenesis precedes itsenhancement of glucose uptake. The addition of prolactin toinsulin-containing cultures has little effect on glucose uptakeand lipogenesis, but stimulates minimal secretion in alveolarlumina. The absence of intracellular vacuoles indicates thatthese products probably contain little lipid. Corticosteroneenhances the effects of insulin on lipid synthesis, but haslittle apparent effect on the secretory morphology of the alveoli. The three-hormone combination has no effect on glucose uptakeabove that obtained with insulin alone; however, it inducesmarked increases in Iipid synthesis as well as maximal morphologicalsecretion by 48 hr. Thus, as for other lactogenic responsesin vitro, insulin, prolactin, and corticosterone act synergisticallyto stimulate lipid synthesis in mammary explants.     

Effect of Phosphorus Deficiency and Water Deficit on Phosphatase Activities from Wheat Leaves

Wheat was sown in a phosphorus (P) deficient soil. Plants atlow levels of applied P had lower growth rates and lower concentrationsof phosphate in the shoots than plants grown with ‘highP’. Activities of both insoluble and soluble phosphataseincreased with P deficiency in the mature leaves. Soluble phosphataseactivities increased 2.5–3.0 fold as the concentrationof phosphate in the leaves fell from 0.4% to 0.1% dry weightThis increase was not a consequence of reduced growth, as severenitrogen deficiency had no effect on phosphatase activity. Soluble phosphatase activities were higher in young than inmature leaves, and also increased 3–4 fold with severewater deficit. However these increases in activity were notaccompanied by low concentrations of phosphate. Moreover, solublephosphatase activities in mature leaves of plants grown underconditions of water deficit rapidly decreased after rewatering.In contrast, the high soluble phosphatase activities in matureleaves of P deficient wheat persisted for up to 12 d after theresupply of P to adequate levels.     

The Effects of Copper Supply and Shading on Retranslocation of Copper from Mature Wheat Leaves

Plants of Gamenya wheat (Triticum aestivum L.) were grown inpots of a Cu-deficient sand at two levels of Cu (deficient andsufficient), and harvested on days 13, 22, 28 and 38. In 50per cent of the pots in each Cu treatment, the oldest leaf andleaf 2 of the main stem were shaded when they reached full expansion. The Cu content of the oldest leaf of Cu-sufficient, unshadedplants was high at day 13 and declined rapidly to day 38. Thatof Cu-deficient, unshaded plants was initially relatively lowand declined much more slowly, so that at day 38 it resembledthat of Cu-sufficient plants. Shading the oldest leaf acceleratedthe loss of its Cu in both Cu-deficient and Cu-sufficient plants.The effects of shading and of Cu supply on the loss of Cu fromthe oldest leaf paralleled their effects on the loss of N andchlorophyll. The results suggest that most of the Cu in theoldest leaf does not move out until the leaf senesces. In Cu-deficient plants retention of Cu by old green leaves accentuatedCu deficiency. The release of Cu, resulting from shading theold leaves of Cu-deficient plants, stimulated the growth ofnew leaves. In Cu-sufficient plants, shading depressed growth. copper, shading, retranslocation, wheat, Triticum aestivum L.     

The Effect of Copper Supply on the Senescence and the Retranslocation of Nutrients of the Oldest Leaf of Wheat

The contents of Cu, N, P, K, Zn, Mn and Ca were followed duringthe life of the oldest leaf of wheat plants (Triticum aestivumL. cv. Gamenya) grown at deficient and sufficient supplies ofCu. At both levels of Cu, the Cu content of the oldest leafbehaved in a similar way to the contents of N and Zn, whichdeclined markedly during leaf senescence. By contrast to Cu the P and K contents declined markedly, priorto leaf senescence, whereas the Ca and Mn contents increasedthroughout the life of the leaf and did not decline during leafsenescence. Interactions among Cu supply, the supply of other nutrients(e.g. N), and leaf senescence account for the variable mobilityof Cu in wheat. Similar interactions between nutrient supplyand senescence may explain contradictory reports on the redistributionof other nutrients which are variably mobile in plants.     

The Growth and Carbon Economy of Selection Lines of Lolium perenne cv. S23 with Differing Rates of Dark Respiration: 1. Grown as Simulated Swards During a Regrowth Period

Simulated swards of each of two selection lines of Lolium perennecv. S23 with ‘fast’ and ‘slow’ ratesof ‘mature tissue’ respiration were establishedin growth rooms at 20/15 °C day/night temperatures and studiedover four successive regrowth periods of 46, 30, 26 and 53 daysduration. The ‘slow’ line outyielded the ‘fast’,both in harvestable shoot (above a 5 cm cut) and in root andstubble. Its advantage increased over successive regrowth periodsto 23 per cent (total biomass). Gas analysis measurements onthe entire communities (including roots), during the final regrowthperiod, showed that the ‘slow’ line had a 22–34per cent lower rate of dark respiration per unit dry weight.This enabled it to maintain its greater mass of tissue for thesame cost in terms of CO₂ efflux per unit ground area. Halfthe extra dry weight produced by the ‘slow’ line,relative to the ‘fast’, could be attributed to itsmore economic use of carbon. The rest could be traced to a 25per cent greater tiller number which enabled the ‘slow’line to expand leaf area faster (though not at a greater rateper tiller), intercept more light and fix more carbon, earlyin the regrowth period. Lolium perenne L., ryegrass, respiration, maintenance respiration, tiller production, simulated swards, canopy photosynthesis, carbon economy     

Seasonal Changes in the Physiology of S24 Perennial Ryegrass (Lolium perenne L.): 4. Comparison of the Carbon Balance of the Reproductive Crop in Spring and the Vegetative Crop in Autumn

Measurements of CO₂ exchange were used to construct a detailedaccount of the carbon economy of established simulated swardsof perennial ryegrass during 10 week periods in spring and autumn.Changes in sward dry weight estimated from gas exchange measurementsclosely matched observed changes in dry weight. In spring, light energy increased, the photosynthetic potentialof the canopy increased, and together these factors led to apattern of increasing photosynthetic uptake. In autumn, decreasinglight energy and decreasing canopy photosynthetic potentialled to decreasing photosynthetic uptake. During the periodsinvestigated, the changes in light energy receipt played themajor role in determining the pattern of photosynthetic uptake. A simple model of crop growth was used to illustrate the effectof such characteristic seasonal differences in the pattern ofphotosynthetic uptake on the subsequent loss of carbon duringrespiration and tissue death, and consequently on the productionof live tissue. The model describes how a reproductive cropin spring may accumulate more living dry matter than a vegetativecrop in autumn from the same total gross photosynthetic uptakeof carbon. Lolium perenne L., ryegrass, carbon economy, photosynthesis, respiration