The possible involvement of adenyl cyclase and cyclic-AMP phbsphodiesterase in the formation of crown-gall tumors on the the primary leaves of Pinto beans

Adenyl cyclase activity was found in crown-gall tumor tissueobtained from the inoculation of the primary leaves of Pintobeans with Agrobacterium tumefaciens strain B6. Consistentlymore enzyme activity was found, however, in normal leaf tissueor wounded leaf tissue inoculated with sterile broth than inthe tumor tissue. On the other hand, cyclic-AMP phosphodiesteraseactivity increased with tumor age. These two enzymes were also found in extracts of both infectiousand non-infectious strains of Agrobacterium tumefaciens, althoughno obvious correlation between the production of these enzymesand infectivity could be established. Some of the implicationsof these results will be discussed. (Received May 25, 1976; )     

Studies in the Physiology of Parasitism: XVI. Effect of the Condition of Potato Tissue, as modified by Temperature and Water-content, upon Attack by Certain Organisms and their Pectinase Enzymes

1.Certain bacteria which are normally termed saprophytic, viz.Bacillus subtilis and B. megatherium, are able to parasitizeliving potato tissue at a suitably high temperature or whenthe tissue is injected with water. 2.Within the group of four bacteria tested, there is a correlationbetween capacity to attack potato tissue and amount of pectinaseenzyme excreted under standard conditions. 3.A qualitative difference between the pectinase enzymes ofBotrytis cinerea and Bacterium carotovorum has been demonstrated.Preparations of the bacterial enzyme, which when tested on turgidpotato discs of standard thickness were found to be weaker thanBotrytis enzyme, were able to attack normal (subturgid) potatotissue, whereas the Botrytis enzyme failed to do so. No explanationof this difference is yet forthcoming. It does not seem to restupon osmotic differences between the two enzymic preparations. 4.Rate of diffusion appears .to be a limiting factor in theattack of potato tissue by preparations of pectinase enzyme.     

The concentration of selected cations in normal and crown-gall tumors obtained from potato discs

Crown-gall tumor tissue obtained from potato discs inoculatedwith virulent strains of Agrobacterium tumefadens containedhigher concentrations of K⁺, Mg²⁺ and Ca²⁺ than the correspondingnormal tissue. These tumors also contained higher concentrationsof these cations than normal tissue inoculated with an avirulentstrain of Agrobacterium tumefadens, or than normal tissue adjacentto the crown-gall tumors on the same potato disc. The concentrationof these cations remained significantly higher than controltissue regardless of the tumor age. 2,4-Dinitrophenol and myo-inositol,while affecting the concentration of Ca²⁺ in these tissues,had no effect on the Mg²⁺ and K⁺ concentrations. These resultssuggest increased concentrations of certain cations may be aspecific property of crown-gall tumors. (Received August 16, 1978; )     

Studies in the Physiology of Parasitism: XXIII. On the Parasitic Vigour of Certain Bacteria in Relation to their Capacity to Secrete Pectolytic Enzymes

1. 1. Three organisms, Flavobacterium sp., Pseudomonas sp. designatedNo. 169 and Pseudomonas syringae, were compared with a pathogenBacterium aroideae. Although they all produced pectolytic enzymeof equal activity on potato extracts, only the pathogen wasable to parasitize the vegetable tissue, except when the watercontent of the latter was increased.
2. 2. It was evident thatsuccess or failure of an attack was determinedwithin 24 hoursfrom inoculation. The events taking place duringthis periodwere studied in some detail with potato extractsand potatotubers. On dilute extracts the pathogen grew rapidly,with anacid drift of the medium, and pectolytic enzyme wasdetectablewithin a few hours from inoculation. The weaker organismsgrewslowly, with no acid-forming tendency, and showed a delayinenzyme secretion. Differences in growth and in secretionofenzyme were further accentuated when the extract approachedthe strength of potato sap.
3. 3. No obvious qualitative differenceswere found between thepectolytic enzymes secreted by the fourorganisms.
4. 4. The failure of the weak organisms to attacknormal potatotissue can be ascribed to their slower rates ofgrowth and enzymicsecretion which allow the host time to forma protective barrier.On the other hand, rapid growth and thesecretion of enzymewithin a few hours enabled B. aroideae tobecome establishedbefore a wound reaction could take place.

     

Human thyroid cyclic nucleotide phosphodiesterase. Its characterization and the effect of several hormones on the activity.

Cyclic AMP and cyclic GMP phosphodiesterase activities (3',5'-cyclic AMP 5'-nucleotidohydrolase, EC 3.1.4.17) were investigated in the human thyroid gland from patients with hyperthyroidism. Low substrate concentration (0.4 muM) was used. About 60% of the cyclic-AMP and 80% of the cyclic-GMP hydrolytic activities in the homogenate were obtained in the soluble fraction (105 000 X g supernatant). The thyroid gland contains two forms of cyclic-AMP phosphodiesterase, one with a Km of 1.3-10(-5) M and the second with a Km of 2-10(-6) M. Cyclic-AMP and cyclic-GMP phosphodiesterase were purified by gel filtration on a Sepharose-6B column. Cyclic-AMP phosphodiesterase activities were found in a broad area corresponding to molecular weights ranging from approx. 200 000 to 250 000 and cyclic-GMP phosphodiesterase activity was found in a single area corresponding to a molecular weight of 260 000. Cyclis-AMP phosphodiesterase activities were stimulated by the protein activator which was found in human thyroid and this stimulation was dependent on Ca2+. Stimulation of cyclic-AMP phosphodiesterase by the activator was not significant even in the presence of enough Ca2+. The effect of D,L-triiodothyronine, D,L-thyroxine, L-diiodotyrosine, L-monoiodotyrosine, L-thyronine, L-diiodothyronine, thyrotropin, hydrocortisone, adrenocorticotropin, cyclic-AMP and cyclic-GMP on the phosphodiesterase activities was studied. Cyclic-AMP, cyclic-GMP, D,L-triiosothyronine, D,L-thyroxine, adrenocorticotropin and hydrocortisone where found to inhibit the phophodiesterase. Triiodothyronine and thyroxine inhibited cyclic-AMP phosphodiesterase more effectively than cyclic-GMP phosphodiesterase. Thyroxine was a more potent inhibitor than triiodothyronine. The concentration of cyclic AMP producing a 50% inhibition of cyclic-GMP phosphodiesterase activity was 5-10(-5) M, while the concentration of cyclic GMP producing a 50% inhibition of cyclic-AMP phosphodiesterase was 3-10(-3) M. Both cyclic-AMP and cyclic-GMP phosphodiesterase activities in the homogenate of hyperthyroidism, thyroid carcinoma and adenoma were higher than in normal thyroid tissue, when assayed with a low concentration of the substrate (0.4 muM). When a higher concentration (1 mM) of cyclic nucleotides was used as the substrate, cyclic-AMP hydrolytic activity in adenoma tissue was similar to that of normal tissue, while the other activities were higher than normal.     

Calmodulin activation of cyclic AMP phosphodiesterase in the B16 mouse melanoma

Mouse B16 melanoma extracts of both cultured cells and tumour tissue contain cyclic AMP phosphodiesterase activity, with 95% present in the soluble fraction. Although activation of the enzyme by added calmodulin did not occur, it was found that endogenous calmodulin was present at a level sufficient to activate fully the enzyme. The ability of Ca-calmodulin to stimulate cyclic AMP phosphodiesterase in this tissue was shown by the inhibitory effect of N-(6-aminohexyl)-5-chloronaphthalenesulphonamide (W7), a known calmodulin antagonist; by the activation of the enzyme with exogenous calmodulin observed in supernatants depleted of endogenous calmodulin by passage over fluphenazine-Sepharose 6B in the presence of Ca2+; by the Ca-dependent binding of the enzyme to calmodulin-agarose and its activation by Ca-calmodulin after elution from the column with EGTA-containing buffer. It was calculated that about 50% of the total cyclic AMP phosphodiesterase activity was calmodulin-activated in this tissue.     

Interaction between rhizobia and potato tissues10

Several cultivars of Solanum tuberosum L., the potato, weregrown on tissue culture media and their roots inoculated withstrains of rhizobia known to infect legumes at root junctionsor between epidermal cells. Infection incidence and severityshowed considerable cultivar/bacterial strain interaction. Bacteriaspread through intercellular spaces and invaded cells in a non-structuredway: some infections penetrated to the root xylem. There wasno evidence that potato root cells produced nod-inducing factorsand nitrogenase activity was not detected. In some host/rhizobialcombinations outgrowths were formed on roots. These varied fromloose infected callus tissue at the junctions of lateral roots,to modified lateral roots of limited growth which showed somecolonization by rhizobia. Key words: Solarium tuberosum L, potato, glycoprotein, immunogold labelling, rhizobia, flavonoids     

Studies in the Physiology of Parasitism: XVII. Enzyme Secretion by Strains of Bacterium carotovorum and other Pathogens in relation to Parasitic Vigour

1. When tested on potato tubers and roots of turnip, swede,and carrot, the organisms Bacterium aroideae, B. carotovorum(i), B. carotovorum (ii), and Phyto-monas carotae show diminishingpathogenicity in the order named. Attack on potato is greatestat 25–35° C., and falls off gradually from 20°to 10°, below which it ceases. 2. The susceptibility of potato tubers rises as they grow tofull size but falls during the dormant period. With the activeparasite B. avoideae there is a considerable rise in susceptibilityas the tuber reaches the storage of sprouting. 3. Susceptibility of potato tubers is increased by storage forsome time at an elevated temperature (c. 35° C.), or byrasing their water-content, either by soaking or by direct injection,and especially by the latter. Similar responses to these treatmentsare given by enzymic preparations of the bacteria. 4. The greater pathogenicity of B. avoideae than of the carotovorumstrains is associated with a greater rate of multiplicationof the former under comparable conditions and with a greatertendency of teh latter to an acid-forming type of metabolismwhich is unfavourable to multiplication of the organism andto the activity of its enzyme.     

Factors Affecting the Formation of In vitro Tubers of Potato (Solanum tuberosum L.)

In vitro (mini) tubers were induced within 6–8 weeks inserially propagated potato shoot cultures by subculturing tomedium containing 2.0 mg 1^–1 benzylaminopurine (BAP) and6 per cent sucrose in 8- and 24-h days. The effect of BAP inpromoting tubering was greater in short than in long days. Inshort days most of the tubers were formed above the agar, inlong days within the agar. Tubering was promoted less effectivelyby the addition of (2-chloroethyl)-trimethylammonium chloride(CCC) to the medium, but CCC reinforced the effect of BAP leadingto earlier tubering above the agar. Tubering eventually tookplace after 4—5 months on medium without hormones, soonerin short than in long days. Periods of short days and low temperaturesgiven to long-day cultures did not accelerate tubering. Abscisicacid had little effect on, and GA2 strongly inhibited, tubering.Tubering was also inhibited by sealing the culture vessels butnot if ethylene-absorbing agents were included. Solanum tuberosum L, potato, tissue culture, tubers, cytokinin, ethylene, daylength, propagation     

Inhibition of crown-gall tumor formation on potato discs by cyclic-AMP and prostaglandins E1 and E2

Cyclic-AMP was found to inhibit the induction of crown-galltumors on potato discs by as much as 60%. This inhibition couldbe obtained when cyclic-AMP was added up to 10 hr after inoculationof the potato discs with a tumor inducing strain of Agrobacteriumtumefaciens. Similar results were obtained with prostaglandinsE¹ and E². Some of the implications of these results will bediscussed. (Received September 30, 1976; )     

Distribution of {beta}-Thioglucosidase Activity in Intact Plants, Cell and Tissue 6Brassica napus L.

Distribution of myrosinase activity in extracts from seeds,intact plants, cell cultures and regenerated callus and plantsof Brassica napus L. was determined by the rate of glucose formationfrom glucosinolate hydrolysis. Calli with shoots and regeneratedplants were obtained from protoplasts or from explants. Of the seedling organs from Brassica napus L. cv. Niklas, hypocotylsshowed the highest myrosinase activity. In cotyledons a nearlyconstant enzyme activity was determined over the first 6 d,followed by a gradual decline. Roots showed a fast decline inenzyme activity over the investigated period. Freshly-isolated protoplasts contained less myrosinase activitythan the original intact tissue. The enzyme activity in developingcalli generally decreased during the first culture periods.After the initial decline a low activity was found which wasstable for a period of more than 2 years. The enzyme activityshowed fluctuations when measured at different times after mediumchange. Protoplast calli with regenerated shoots showed a considerablyhigher myrosinase activity than calli without shoots. Myrosinaseactivity was also found in explant calli including explant callifrom cotyledons and hypocotyls after induction of shoots. Myrosinase activity in seeds from 21 cultivars of Brassica napus,Brassica campestris, Sinapis alba and Raphanus sativus was testedand the highest myrosinase activity was found in seeds fromthe Sinapis alba cultivar Trico while the lowest activity wasfound in the Brassica campestris cultivar Rapido III. Leaf, stem and inflorescence from flowering regenerated or seed-grownplants contained a low but significant myrosinase activity.In contrast, roots showed a high myrosinase activity. The resultsobtained from regenerated plants indicate that the myrosinasesystem is stable in vitro culture, and that the glucosinolate-myrosinasesystem is active in calli tissue. Key words: Myrosinase (thioglucoside glucohydrolase, E.C. 3.2.3.1), in vitro cultures, intact plants     

Increase in Catalase mRNA in Wounded Sweet Potato Tuberous Root Tissue

Catalase protein, as well as its activity, increases in woundedsweet potato tuberous root tissue [Esaka et al. (1983) PlantCell Physiol. 24: 615]. Whether catalase mRNA increases in woundedtissue was examined with a hybridization probe of a cDNA forsweet potato catalase mRNA. The content of catalase mRNA inthe tissue increased after a lag phase of 10 h to reach a maximumat 30 h after wounding, whereas total RNA content increasedwithout a lag phase. The increase in the mRNA content afterthe lag phase preceded that in catalase activity. In the earlystages after wounding, catalase mRNA in polysomes increasedin spite of no increase in the total content of mRNA in thetissue. We propose that an increase in catalase mRNA is responsiblefor the increase in catalase protein in wounded sweet potatotuberous root tissue. In the early stage after wounding, however,the translation of catalase mRNA seems to be activated throughincreased availability of ribosomes. (Received January 28, 1987; Accepted May 6, 1987)     

Biosynthesis of furano-terpenes by sweet potato cell culture

Callus was induced from sweet potato root tissue on an agarmedium containing Heller's minerals, vitamins, 2,4-D, yeastextract and sucrose. Furano-terpenes were scarcely detectedin the callus. However, when the callus was transferred to aliquid culture medium and incubated with reciprocal shaking,furano-terpenes were rapidly produced mainly in the culturemedium. Furano-terpene production by the cell culture was suppressedby addition of Ceratocystis fimbriata spores or HgCl₂ to theculture medium. Yeast extract and sucrose in the culture mediumwere important for furano-terpene production. 3-Hydroxy-3-methylglutarylcoenzyme A (HMG-CoA) reductase activity increased in the cells,followed by the production of furano-terpenes. The TLC patternof furano-terpenes produced by the cell culture was essentiallythe same as that produced by sweet potato root tissue infectedby C. fimbriata or treated with HgCl₂, but the quantitativeproportion of the individual furano-terpenes in the former differedmarkedly from that in the latter. (Received January 11, 1979; )     

Effects of Deltamethrin on Field Grown Potato Plants:Biochemical and Ultrastructural Aspects

The effects of repeated spraying of field grown plants of Solanumtuberosum L. with deltamethrin 24, 41 and 55 d after emergence,on chlorophyll level, oxygen uptake, RuBisCo activity and leafultrastructure, were studied. Chlorophyll amount increased in treated plants after the secondand third spraying, whereas RuBisCo activity showed a highervalue than in the controls only after the last treatment. Incontrast, the respiratory activity was stimulated by the firstspraying and no significant differences were found with theensuing treatments. The general ultrastructure of mesophyllcells was not altered by deltamethrin, but morphometric analysisof electron micrographs showed that the fractional volume ofchloroplasts and starch in the treated leaves were consistentlylower than in controls. The biochemical and ultrastructural data suggested that thevegetative cycle of the sprayed plants had been extended.Copyright1993, 1999 Academic Press Solanum tuberosum L., potato plant, deltamethrin     

Production of ethylene by sweet potato roots infected by black rot fungus

Ethylene production by sweet potato roots infected by the blackrot fungus, Ceratocystis fimbriata, increased strikingly afterinfection. The fungus grown on potato extract containing 1%sucrose or steamed sweet potato produced no ethylene. Thus,ethylene was proven to be produced from the host tissue affectedby fungus invasion. The ethylene production seemed to be stimulatedby carbon dioxide. Oxygen was essential for production, butexcess oxygen, probably over 80%, was found to be inhibitory.Apparent fungus growth on sweet potato was reduced under a hightension of oxygen, but this was not a cause of reduced ethyleneproduction in excess oxygen. When tissue plugs of infected sweet potato which were activelyproducing ethylene were sliced into thin discs, ethylene productionwas abolished with the exception that the first 1 mm discs atthe 1st and 2nd day stages produced a significant amount ofethylene. Similarly, plugs which were removed from fungus-invadedparts did not produce an appreciable amount of ethylene. Theproduction of ethylene was observed only by tissue plugs whichconsisted of both fungus invaded and noninvaded parts. Infected sweet potato tissue produced ethylene at a rate comparableto that in apples and may provide a goodsystem for the studyof ethylene biosynthesis. ¹Part 72 of the Phytopathological Chemistry of Sweet Potatowith Black Rot and Injury.     

Polyamines and crown gall tumor growth

The effect of the polyamine spermidine on the growth of crown gall tumors was determined using the potato disc bioassay. Addition of lmM spermidine resulted in a 30–50% increase in tumor growth. The spermidine effect was found to be biphasic, with lmM being optimal. Closely related polyamines including spermine, as well as other nitrogen containing compounds such as arginine and alanine, failed to promote tumor growth or inhibited the growth of these tumors. Endogenous levels of spermidine in crown gall tumor tissue were consistently greater than those of corresponding normal potato tissue. Rapidly dividing normal potato tissue derived from buds also contained elevated spermidine levels.     

Potato Lectin: A Cell-Wall Glycoprotein

The activity and the amount of potato lectin were measured inpotato tuber slices (Solanum tuberosum cv. Huinkul) aeratedfor 48 h. Lectin was found in a soluble form, liberated to themedium and associated with insoluble structures. Polyacrylamidegel electrophoresis in denaturating conditions and immunologicaltechniques indicated that the lectins associated to cell wall,soluble or liberated to the medium, were identical. The cell-wallfraction was found to contain 65% of total lectin in the tuber.The possible role of potato lectin in tubers was discussed. (Received June 5, 1985; Accepted September 3, 1985)     

Metabolism of Adenine in Healthy and Blighted Potato Leaves

Analysis of the distribution of ¹⁴C in extracts prepared fromleaf tissue which had been exposed to labelled adenine by petiolaruptake revealed that this purine is extensively metabolizedin both healthy and Phytophthora-infected potato leaves. Incorporationof labelled adenine into the major ribonucleic acid speciesof the leaf was also extensive as determined by radioactiveassays performed on individual fractions which were separatedon columns of methylated albumin kieselguhr. Examination ofindividual nucleotides released by alkaline hydrolysis showedthat both the adenylic and guanylic acid moieties were labelled.Although the labelling patterns were similar for RNA from healthyand infected leaf tissue, the specific activity of the latterwas consistently higher than the former. When partially purified leaf extracts were assayed for phosphoribosyltransferase,they exhibited relatively high levels of activity with adenineas substrate, but were virtually devoid of activity with hypoxanthineand guanine. However, direct petiolar uptake of labelled hypoxanthineresulted in highly labelled RNA. A comparison of adenine phosphoribosyltransferase activity inextracts from healthy and blighted leaves failed to reveal measurabledifferences. Therefore, it was concluded that the differentialincorporation of labelled adenine into the RNA of healthy andinfected leaves was due neither to increased activity of thisenzyme in response to infection nor to its differential activation. Apart from its role in the recovery of preformed purines fornucleic acid synthesis, adenine phosphoribosyltransferase mayfunction as part of a mechanism for regulating levels of adeninein the potato leaf.     

Mechanism of the Increase in Ribonuclease Activity in Potato Tuber Slices

Upon wounding of potato tubers (Solanum tuberosum L. cv. Spunta)RNase activity increases, peaks in about 16 hours, then declines.To see if the increase of the activity is due to de novo synthesisof the enzyme protein, the extracts were compared for theirability to react with a rabbit antibody prepared against thewound activated RNase. The enzyme was purified by polyacrylamidegel electrophoresis of a RNase preparation, which had been partiallypurified from aged potato slices by ammonium sulfate precipitation,carboxymethyl-Sephadex column chromatography and gel filtrationthrough Sephadex G-100. Using rocket immunoelectrophoresis RNase-proteinimmunoprecipitated by the antibody increased in wounded tissue.This observation implies that the activity increase involvesenzyme synthesis. The increase was inhibited by actinomycinD and cordycepin, but not by 5-fluorouracil, suggesting a requirementfor mRNA synthesis. (Received April 9, 1985; Accepted December 16, 1985)     

A study of cyclic nucleotide metabolism and the histology of rat liver during 3'-methyl-4-dimethylamino-azobenzene carcinogenesis. II. Cyclic AMP metabolism.

We have studied cAMP metabolism in rat livers undergoing carcinogenesis induced by dietary 3'-methyl-4-dimethylaminoazobenzene. A correlation between the biochemical and the histological changes described in the companion paper has been made. In this study, we saw 100% incidence of cholangiocarcinoma by 10 weeks. During weeks 1--10, the biochemistry of tumor-free areas of the livers only was studied; during weeks 11-13, the increased size of the tumors made possible a biochemical study of the tumor tissue as well as the non-tumor tissue, and a comparison between the two was made. Alterations in all parameters of cAMP metabolism were seen from the earliest stages of treatemnt. Most striking were those of adenylate cyclase activity which preceded and accompanied tumor formation, and were seen in both non-tumor and tumor tissue. In the first few weeks of treatment, small acidophilic glycogen-deficient hepatocytes appeared in the periportal areas of the liver lobules. During this time, there was an increase in maximal isoproterenol stimulation of adenylate cyclase and to a lesser extent in the basal activity of the enzyme; increases in phosphodiesterase activity were seen, and were greatest in weeks 1, 2; cAMP levels were diminished in weeks 1, 2 and slightly but not significantly elevated at week 3. From week 4 onwards an even smaller glycogen-deficient cell population appeared in perilobular areas amongst the acidophilic hepatocytes, and tumors began to appear elsewhere in the livers; at this time, there were further marked increases in the basal activity and isoproterenol responsiveness of adenylate cyclase, and the appearance of increased Gpp(NH)p responsiveness of the enzyme; the increase in phosphodiesterase activities seen at week 3 (smaller than that seen in weeks 1, 2) was sustained but did not further increase; cAMP levels were now significantly elevated also, but they did not rise steadily as did the activity of adenylate cyclase. There was a marked difference between the adenylate cyclase activities in non-tumor tissue from tumor-bearing and non-tumor-bearing livers in weeks 4--10, but there was no difference between the phosphodiesterase activities or cAMP levels in these two groups. Adenylate cyclase activity was extremely high in both non-tumor tissue of tumor-bearing livers from weeks 4--10 and tumors from weeks 11--13. Although phosphodiesterase activities were most elevated in the tumors, there were extremely high cyclic AMP levels in these tissues. The difference between the cAMP levels of tumor and non-tumor tissue was striking. Our findings are discussed with respect to the two-state model of carcinogenesis...