Aluminium Effects on ATPase Activity and Lipid Composition of Plasma Membranes in Sugar Beet Roots

The effect of aluminium (Al) in vivo and in vitro on root plasmamembranes has been studied in two sugar beet (Beta vulgarisL.) cultivars, Monohill (Al-sensitive) and Regina (relativelyAl-tolerant). Although Al in vitro inhibited the MgATPase inan uncompetitive way for both cultivars raised in the absenceof Al, the specific K⁺-activation of the MgATPase was only inhibitedby Al in cv. Monohill. Arrhenius analysis of the MgATPase activity showed that theeffect of Al in vitro depended on whether or not the plantswere exposed to Al in vivo. Al treatment in vitro of the MgATPasefrom control plants cultivated at a low pH (5·4) causedan increase in the phase transition temperature from 17 to 22°C. Only at a higher pH range (pH 6·1) could a secondtransition temperature be induced (at 9 °C). By additionof Al in vitro to plants cultivated with Al at pH 5·4,the slopes of the activity plots did not change. Aluminium changedthe K_m of the ATPase for MgATP in an opposite way by treatmentin vivo and in vitro. Lipid analyses of the plasma membranes showed that the acylcomposition differed little following Al treatment in vivo,but that the ratio of phosphatidylcholine: phosphatidylethanolamineincreased. The changes correlated with the observed change inthe K_m for the MgATPase. We conclude that the main effect ofAl on the MgATPase is not due to the formation of an Al-ATPcomplex. Instead, Al may bind to the membrane-bound enzyme(s)and/or modify the lipid environment. Key words: Aluminium, ATPase, Beta vulgaris, lipids     

Structure--function studies of oligosaccharides of recombinant human thyrotrophin by sequential deglycosylation and resialylation

Recombinant human thyrotrophin (rhTSH) contains oligosaccharidesterminating in -galactose-sialic acid, and had lower metabolicclearance and higher in vivo bioactivity compared to pituitaryhTSH, which has oligosaccharides terminating predominantly in-N-acetylgalactosamine-sulphate. Previous studies using completeremoval of the oligosaccharide chains showed an important rolefor the carbohydrate in the biological activity of the hormone.In the present study, we have determined the contribution ofthe individual monosaccharides to hormonal activity by sequentialdeglycosylation of rhTSH using exoglycosidases. We have alsoinvestigated the effect of resialylation of desialylated rhTSHusing sialyltransferases. Sequential removal of sialic acid,galactose or N-acetylglucosamine resulted in a > 10-foldincrease in the in vitro bioactivity of rhTSH. The metabolicclearance of the derivatives was faster than that of intacthormone, but agalacto-rhTSH was cleared slower than asialo-rhTSH.However, the in vivo bioactivity decreased progressively witheach monosaccharide removal. The increased cyclic AMP-stimulatingactivity, increased metabolic clearance and the decreased invivo biologic activity were all reversed by resialylation ofthe terminal galactose residues. These results indicate thatthe in vitro, as well as the in vivo, bioactivities of rhTSHare modulated by terminal sialylation. The effects of sequentialdeglycosylation on the in vitro activity of rhTSH are differentfrom those reported earlier for human chorionic gonadotrophin.Thus, modification of the oligosaccharides by glycosidases andglycosyltransferases can be used as a powerful tool to delineatethe function of carbohydrate in glycoproteins and to engineermore potent hormone analogues with a longer half-life and/orhigher bioactivity. deglycosylation exoglycosidases oligosaccharides recombinant thyrotrophin sialyltransferases     

Differential expression of an endogenous mannose-binding protein R1 during muscle development and regeneration delineating its role in myoblast fusion

The role of the endogenous brain carbohydrate-binding proteinR1 in muscle cell development and regeneration was analysedboth in vivo and in vitro. In vivo, R1 was developmentally regulated,with an embryonic 65 000 subunit and a neonatal 67 000 subunit,being replaced progressively by a 135 000 adult form. LectinR1 was intracellularly localized at birth and in the prenatalperiod. During development and at the time of myoblast fusion,the antigen was progressively found at the surface, where itremained at low levels in the adult. In vitro, in pure myoblastcultures, only the embryonic form was present. The ultrastructuralstudies indicated that the lectin could participate in the membranefusion process during myoblast fusion. The specific role inmyoblast fusion, derived from the ultrastructural localizationof R1, was evidenced by a strong inhibitory effect of anti-R1 Fab fragments (10–100 µg/ml), relative to controlFab fragments. In vivo, the embryonic subunit pattern and subcellulardistribution of R1 reappeared in muscle cells after lesion ofthe adult muscle. This suggested that, as observed in vitro,R1 participated in vivo in the phenomenon of myoblast fusion.Similar modifications in subunit expression were observed inmuscles after denemation (the embryonic form of lectin R1 reappearingafter lesion), suggesting that R1 could be involved in the processof neuromuscular junction formation. Thus, it is proposed thatthe carbohydrate-binding protein R1 is an important recognitionmolecule for the formation of myotubes. Its potential involvementin a recognition process between axons and muscle cells duringneuromuscular junction formation is discussed. culture development fusion N-glycan glycoprotein lectin mannose myoblast     

Hormonal Regulation of Cormel Formation in Gladiolus Stolons Grown in vitro

The influence of four plant hormones on cormel development inGladiolus stolon tips grown in vitro was tested. Kinetin inducedcormel formation while Gibberellin A₃ inhibited it at low kinetinlevels. Abscisic acid did not affect cormel formation, but inhibitedtheir growth. Naphthalene acetic acid had no direct effect ontuberization. Anatomical observations revealed no differencesbetween cormels formed in vitro and in vivo.     

槲皮素对黄粉虫血淋巴酚氧化酶的生理效应

用酶标仪法测定了槲皮素对黄粉虫Tenebrio molitor酚氧化酶（phenoloxidase, PO）的生物活性。结果表明：在离体条件下,对黄粉虫血淋巴PO的IC₅₀为0.625 mmol/L。在活体情况下,当槲皮素-DMSO溶液或槲皮素水悬浮液（5 μL）注入虫体后,在浓度低于1.0 mmol/L时对黄粉虫血淋巴PO具有激活作用,当浓度高于2.0 mmol/L时则对PO具有明显的抑制作用;单独注射5 μL DMSO溶液对PO活性亦有一定的激活作用。试虫被注射槲皮素后,PO活性在2～4 h内迅速下降,然后缓慢上升,处理8 h左右达到最高点,其后低浓度处理PO活性保持不变,而高浓度处理则逐渐下降,提示低浓度槲皮素可以引起试虫的免疫反应。在PO测活体系中加入0.5％的BSA后对PO活性无影响,并能使槲皮素在测活体系中保持稳定。     

Establishment of in vitro Cultures of Tapinanthus bangwensis (Engler and K. Krause) Danser and the Effects of Sugars on Growth

Culturing of organs in vitro has been successfully employedin studies on morphogenesis and nutritional requirements ofparasitic and semi-paraaitic angiosperms. Tapinanthus bangwensis,a semi-parasite, has been successfully cultured on chemicallydefined media. By and large the parasite will thrive well ina medium of mineral salts and sucrose at its optimal concentration(4 per cent). However, the parasite is able to metabolize awide range of sugars most of which show similar concentrationoptima Although the growth in vivo was simulated in vitro inthe early stages, it was found that in the later stages growthin vitro was much slower than growth in vivo. The growth differencesobserved in the different media may reflect some of the physiologicaldifferences that are responsible for the selective nature ofthe parasite's development and establishment on different hosts     

Efficacy of Fungicides for Control of Phytophthora Leaf Blight of Taro

Six fungicides were evaluated under greenhouse, laboratory,and dryland field conditions for control of Phytophthora leafblight of taro incited by P. colocasiae. Five separate criteriawere utilized to evaluate these fungicides: fungicidal activityin vitro; and fungicidal activity in vivo under conditions ofsimulated dew, simulated rainfall, greenhouse, and dryland fieldenvironments. In in vitro tests zoospores were killed at thefollowing concentrations: Dithane M-45, 5 ppm; Difolatan, 9ppm; Polyram, 65 ppm; Tribasic Copper Sulphate, 145 ppm; Benlate,210 ppm; and Dyrene, 260 ppm. Excellent control was obtainedwith Difolatan; good control with Dithane M-45 and Polyram;and poor control with Benlate, Tribasic Copper Sulphate, andDyrene. Results of in vivo tests correlated with those of thein vitro tests. Difolatan, Benlate, and Dyrene were the mostphytotoxic while Tribasic Copper Sulphate, Polyram, and DithaneM-45 were the least phytotoxic.     

Respiration and Mitochondrial Activity in Zea mays Roots As Affected by Osmotic Stress

Studies were made of metabolism in highly vacuolated and slightlyvacuolated Zea mays root tissue both during and after plasmolysis. Plasmolysis resulted in decreased respiration and carbon dioxideevolution from glucose and an increased sucrose synthesis. Inhibitionof respiration during plasmolysis in both the highly vacuolatedand slightly vacuolated tissue was not relieved by supply ofglucose, organic acids, or uncouplers of oxidative phosphorylation.Mitochondria isolated from plasmolysed tissue were tightly coupled,but activity in vitro was inhibited by exposure to a high negativeosmotic potential. It is suggested that low TCA cycle activityin vivo must be due either to inhibition of mitochondrial activityor to reduced flow of carbon through the glycolytic pathway. A low potential for TCA cycle activity after deplasmolysis issuggested, as addition of pyruvate stimulated carbon dioxideevolution but not oxygen uptake, which was severely decreased.This was presumably due to severe mitochondrial damage as shownby their activity in vitro. However, it is not clear whetherrespiration in vivo is rate limited by rapid leakage of metabolicintermediate (reported earlier) or by lysis of mitochondria. Deplasmolysis did not damage mitochondria from slightly vacuolatedtissue, a result which was consistent with respiratory measurementsmade in vivo. The data show that mitochondria in vacuolated tissue are damagedduring and after deplasmolysis and not before. It is suggestedthat lysis of mitochondria occurs in vivo as a result of a sharpincrease in the osmotic potential of the cell fluids.     

In vitro Culture of Immature Cotyledons of Soya Bean (Glycine max L. Merr.)

An in vitro procedure promoting the rapid growth and proteinincrease of soya bean cotyledons has been developed. The amountof protein synthesized varied greatly depending on the nitrogen(N) source provided. Glutamine was the most effective N source,while inorganic forms of N were ineffective. Growth and proteinsynthesis were both more rapid in vitro than in vivo. Underthe best conditions, soya bean cotyledons increased 8-fold bothin dry weight and in protein in 6 days. The formation of the7S and 11S storage proteins in vitro was similar to that invivo. Hence, this in vitro culture method is appropriate forstudying legume seed storage protein synthesis under controlledconditions.     

Ecteinascidia turbinata Extract Activates Components of Inflammatory Responses Throughout the Phylogenetic Spectrum

The tunicate Ecteinascidia turbinata contains a substance orsubstances capable of exerting a number of biological effects.Extracts of tunicate tissues have been shown to kill tumorcells in vitro and arrest tumor growth in vivo. The extractsalso suppress allograft rejection, graft-US.-host reactionsand lymphocyte proliferative responses as well as humoral responsesto immunization. By modifying the conditions, the extracts couldpotentiate antibody responses. In addition, they augment functionsof monocyte-macrophages as evidenced by in vitro phagocytosis,in vivo clearance, and cytotoxic activity against target cells.After studies in mice, we were able to demonstrate that theextracts could activate the phagocytic systems of shrimp, bluecrab, and fish (the American eel). In fish, the intraperitonealroute was superior to the intravenous route for promotion ofphagocytosis, increase in percent presentation of granulocytesand for enhancement of resistance to bacterial infection. Intrarriuscularand intraperitoneal injection led to local inflammation withaccumulation of granulocytes and macrophages.     

Metabolic changes of the Antarctic green alga Prasiola crispa subjected to water stress investigated by in vivo 31P NMR

The energy status and the phosphate metabolism of Prasiola crispduring and after desiccation stress was investigated by in vivo³¹P NMR. The effect of desiccation was simulated by additionof the nonionic osmoticum PEG 200 (polyethylene glycol). Photosynthesisand respiration were effectively inhibited under these conditions.The most notable changes in the in vivo ³¹P NMR spectra werean increase in the cytoplasmic inorganic phosphate signal afterPEG stress, a decrease in the polyphosphates and a lowfieldshift of the core polyphosphate signal followed by an appearanceof extracellular inorganic phosphate. Cytoplasmic pH remainedalmost constant during stress. After a return to control conditions,photosynthesis and respiration recovered within 4 h as wellas the concentrations of the phosphorus metabolites. An as yetunassigned phosphate signal increased in the phosphodiesterregion of the NMR spectra. Simultaneousty, the polyphosphatesignal recovered in intensity and chemical shift. It is suggestedthat phosphate metabolism and complexation of cations to polyphosphatesmay play an important role in the distinct desiccation toleranceof P. crispa. Key words: In vivo ³¹P NMR, Prasiola crispa, desiccation tolerance, polyphosphates     

Developmental and Biochemical Regulation of 'Constitutive' Nitrate Reductase Activity in Leaves of Nodulating Soybean

The developmental profile of ‘constitutive’ nitratereductase activity (cNRA) in leaves of soybean (Glycine max(L.) cv. Bragg) plants at different ages is described. The youngestleaves had most cNRA and the activity dropped off as a newerleaf developed above it. Each leaf had its distinct active periodof in vivo cNRA. This pattern was different in urea-grown andsymbiotically-grown plants (inoculated with Bradyrhizobium japonicumstrain USDA 110), where the latter had no detectable in vivocNRA in older leaves. Urea-grown plants maintained considerablein vivo NRA in such older leaves. When symbiotically-grown plantshad their nodules removed, in vivo cNRA reappeared in olderleaves within 1 d of removal, nearly reaching levels of youngleaves at 3 d after nodule excision. Allantoic acid (ALL), oneof the known transport ureides of soybeans, was implicated asa possible signal molecule from nodules to leaves. Allantoicacid (100 µM) inhibited in vitro c₁ NRA significantly,with 400 µM ALL resulting in complete inhibition. In contrast,allantoin (ALN) had no inhibitive effect on NRA. Inhibitionof c₁NRA by ALL was by a competitive process, judging from Lineweaver-Burkeplots against nitrate. Kinetics showed a constant Vmax of around105 nmol NO₂ mg^–1 protein h^–1 and a K_m for nitrateof 15 mM, which increased to 60 mM in the presence of 200 µMallantoic acid. Non-specific (ionic and pH-related) influenceswere eliminated. Allantoic acid also had a slight stimulatingeffect of in vitro NRA (up about 25% at 400 µM). Thesefindings suggest that c1NRA may be involved in ureide metabolism,rather than in vivo nitrate metabolism. Key words: Root-shoot interaction, nitrogen metabolism, nodulation, symbiosis     

In vitro Growth of Vegetative Tomato Shoot Apices

Explants from the shoot apex of the tomato, comprising the apicaldome and youngest primordium together with small amounts ofsub-apical tissue were cultured for periods of 1 to 4 plastochrons.By the use of a simple parameter, the axillary distance, thegrowth-rate could be accurately monitored throughout each plastochron. Gibberellic acid, coconut milk, and kinetin, in addition tosucrose and inorganic salts, all promoted growth of the apex;a combination of gibberellic acid and coconut milk gave thefastest growth. Temperature had a large effect on the growth-ratewith an in vitro Q₁₀ of 2.1 contrasted with an in vivo Q₁₀ of1.2 over the range of 15 to 25 ?C. On gibberellic acid and coconutmilk at 15 ?C two-thirds of the in vivo growth--rate was sustainedin culture for two plastochrons after which the growth-rategradually declined; at 20 and 25 ?C growth-rates slightly higherthan in vivo rates were sustained for 1 plastochron before amore rapid decline. The anatomy of these in vitro apices wasnormal for 1? plastochrons after which there were small increasesin cell volume in the developing primordium. Reducing the amount of sub-apical tissue drastically reducedthe growth rate but had little effect on the responses to gibberellicacid and coconut milk. Explants are considered to be useful material for studying thechanges that take place in the apex during the course of 1 or2 plastochrons, but inadequate on the media tested for experimentsinvolving longer periods of growth. Explants also provide asensitive assay system for the effects of growth factors onthe rate of shoot apical growth.     

The Culture of Immature Pea Embryos

Pea embryos of a range of developmental stages were culturedin a defined medium in vitro for up to 16 days. The criticalfactor for successful culture was the osmotic pressure of themedium; for the stages studied this was provided by the incorporationof 18 per cent sucrose in the medium. The growth of embryosof a range of genotypes was compared; small seeded genotypescould grow at comparable rates in vitro to those attained invivo. The amount of protein synthesized in vitro was similarto that attained in vivo, whereas slightly higher and lowerlevels of starch and DNA respectively were attained in vitro.The roles of intrinsic and extrinsic factors in regulating embryogrowth were studied by comparing the growth in culture of embryosof different genotypes and of hybrid embryos derived from reciprocalcrosses. embryo culture, pea embryos, hybrid embryos, osmotic pressure     

Experimentally Synthesized Plant Chimeras 2. A Comparison of In vitro and In vivo Techniques for the Production of Interspecific Nicotiana Chimeras

In vitro and in vivo techniques were compared for synthesizingchimeras between Nicotiana glauca Grahm and N tabacum L Interspecificchimeral callus, produced from mixed callus cultures in vitro,was placed on media which favoured only N tabacum shoot formationNone of the 474 regenerated N tabacum shoots incorporated Nglauca cells into their meristems When chimeral callus was regeneratedunder hormonal conditions favouring simultaneous organogenesis,of 397 shoots, only non-chimeral shoots of both species aroseIn vivo, reciprocal splice grafts between species were decapitatedjust above the graft union and treated with or without auxin—lanolinpastes Auxin increased callus formation but inhibited adventitiousshoot formation Three of 209 adventitious shoots arising fromthe graft union were interspecific mericlinal chimeras whichwere later stabilized as periclinal chimeras All three chimerasformed when N glauca was the understock Two of the chimerasarose on untreated shoots which produced no visible callus,indicating that excessive callus formation may be unnecessaryfor multiple cell origin of adventitious shoots to occur Chimeras, tobacco, Nicotiana glauca, Nicotiana tabacum, tissue culture, graft chimeras, callus cultures     

Respiration and Carbohydrate Accumulation in the Water-Stressed Wheat Apex

The effect of water stress on the respiration of the immaturefloral apex of wheat was studied in a controlled environmentand related to changes in water relations, growth, protein synthesis,and solute accumulation. Apex respiration measured in vitropolarographically showed no wounding response and was cyanide-and malonate-sensitive. It decreased with each decrease in apexwater potential _a reaching 40% of the non-stress control rateat –5·0 MPa, irrespective of whether the waterstress was induced by droughting in vivo or non-permeating osmoticain vitro. Apex respiration was not quantitatively related toturgor potential. During drought stress there was a conservation of ethanol-insolubledry matter and water in the apex while ethanol-soluble carbohydratesand amino acids accumulated. The calculated daily import ofsoluble carbohydrate into the apex during the whole droughtstress period remained nearly constant despite falling waterpotential. Respiration of the apex during a drought period wasnot limited by the suistrate supply within the apex.     

Salinity and in vitro Ageing Effects on Primary Photosynthetic Processes of Thylakoids Isolated from Pisum sativum and Spinacia oleracea

The effects of in vitro ageing and salinity of the reactionmedium on the primary photochemistry of photosystem II and thepattern of energy distribution within the photochemical apparatusof thylakoids isolated from Pisum sativum and Spinacia oleraceaare described. Analyses of the low temperature induction curvesof fluorescence emission at 695 and 735 nm and of low temperatureabsorption and fluorescence emission spectra were used to examinethese processes. In vitro ageing over short periods reducedthe photochemical activity and changed the energy distributionwithin thylakoids of P. sativum, but had little effect on thylakoidsof S. oleracea. A synergistic effect of in vitro ageing andsalinity of the reaction medium was observed for P. sativumthylakoids. Ageing effects could be minimized by addition of100 mM NaCl to the resuspension medium. Changes in NaCl concentrationin the reaction medium produced large and similar changes inthe primary photochemical functioning of thylakoids from P.sativum and S. oleracea, which could be attributed mainly tothe cation species, Na^$; however, experiments using mannitolto produce osmotic stress indicated some small osmotically inducedchanges in photofunction of the thylakoids. Optimal primaryphotochemical activity of photosystem II, for both species,was observed with 200 mM NaCl. Cation-induced regulation ofexciton distribution appears to be facilitated by controllingthe degree of energy coupling between the light-harvesting chlorophylla/b complex and the two photosystems, I and II, and not by regulationof coupling between photosystems I and II.     

Fruit Set and Growth in Strawberry, Fragaria x ananassa Duch.

The application of GA₃in aqueous solution to leaves or flowersof hermaphrodite cultivars of strawberry, Redgauntlet and Rabunda,prevented growth of the receptacle despite hand pollination.This inhibitory effect occurred only when GA₃ was applied priorto anthesis. Although viable pollen was produced and germinatedto grow down the styles of treated plants, no seeds were formed.Receptacle growth failed underneath the unfertilized carpels,but the basal region devoid of carpels enlarged and ripened.The effect of GA₃ was the same in vivo and for flowers grownin vitro. ABA and BAP also inhibited growth of pollinated flowersin vitro, but neither substance stimulated growth of the baseof the receptacle. 2-NOA stimulated receptacle growth of pollinatedflowers but did not overcome the inhibitory effect of GA₃. Removal of fertile carpels 9 days after pollination preventedfurther receptacle growth. GA₃ treatment of the bare receptaclere-started growth but was less effective than 2-NOA. No growth substance treatment induced parthenocarpic developmentin these cultivars when unopened buds were emasculated and culturedwithout pollination, although GA₃ induced some swelling of thereceptacle base. Fragaria x ananassa Duch., strawberry fruit set, fruit growth, growth regulators     

Formation of Isodityrosine by Peroxidase Isozymes

Fry, S. C. 1987. Formation of isodityrosine by peroxidase isozymes.—J.exp. Bot. 38: 853–862. Tyrosine residues of extensin are oxidatively coupled in vivoto form isodityrosine bridges, whereas treatment of purifiedextensin with H₂O₂+ peroxidase in vitro yields only dityrosine.Two explanations for the correct mode of coupling in vivo weretested. The first, that the pH of the cell wall is lower thanthat (pH 9-0) at which in vitro experiments have been conducted,provided part of the answer since treatment of L-tyrosine withH₂O₂+peroxidase in vitro at pH 37–5 yielded some isodityrosine.The second, that the wall contains other isozymes of peroxidasethan the basic isozyme usually studied in vitro, appeared unlikelybecause several sharply contrasting isozymes yielded similarisodityrosine: dityrosine ratios from L-tyrosine+ H₂O₂ at anygiven pH. The isozymes were also similar in their ability tooxidize tyrosine-dimers further to higher polymers. It is concludedthat the formation of isodityrosine in vivo is dictated by neighbouringwall molecules, possibly ionically-bound pectins, which modifythe local environment of the tyrosine residues of extensin. Key words: Isodityrosine, peroxidase isozymes, extensin     

Thermotropic Properties of Cellular Membranes in Dormant and Non-Dormant Echinochloa crus-galli(L.) Beauv. Seeds

Steady-state fluorescence polarization measurements with l,6-diphenyl-l,3,5-hexatriene(DPH) were used to monitor thermotropic transitions in microsomalfractions and plasma membrane vesicles isolated from barnyardgrass[Echinochloa crus-galli (L.) Beauv.] seeds during the transititionfrom dormancy to germination. The effect of dormancy-relievingor inactive alcohols on the thermotropic properties of the cellularmembranes was determined both in vivo and in vitro. Membranefractions isolated from dormant seeds showed some discontinuitiesin the Arrhenius plots. In non-dormant or germinating seedscellular membranes showed linear Arrhenius plots over the entirerange of temperature examined. Membrane preparations from imbibedseeds showed a similar pattern in their Arrhenius plots upontreatment with the various alcohols in vitro. The results suggestthat the release from dormancy in seeds is associated with somechanges in their cellular membranes. Key words: Germination, alcohols, thermotropic transition