Hevamine: A crystalline basic protein from Hevea brasiliensis latex

The isolation and purification of a basic protein from the bottom fraction of Hevea brasiliensis latex is described. Two protein fractions were obtained by chromatography on carboxymethyl cellulose which also differed in their electrophoretic mobility in polyacrylamide gel, but the similarity of their other properties precludes their classification as two protein entities at this stage.     

Polyphenol oxidases from latex of Hevea brasiliensis: purification and characterization

Polyphenol oxidase (PPO) was isolated from the B-serum obtained after repetitive freeze-thawing of the bottom fraction isolated from ultracentrifuged fresh latex. The B-serum was subjected to acetone precipitation and CM-Sepharose chromatography, affording two PPOs, PPO-I and PPO-II, which, upon SDS-PAGE, were 32 and 34 kDa, respectively. Both PPOs possessed the same pI (9.2), optimum pH (7) and optimum temperature (35-45 degrees C). They are stable up to 60 degrees C and active at broad pH ranges from 4-9. The K(m) values of PPO-I for dopamine, L-dopa and catechol as substrates are 2.08, 8.33 and 9.09 mM, while those for PPO-II are 2.12, 4.76 and 7.14 mM, respectively. Among various PPO inhibitors tested, 4-hexylresorcinol was the most potent. Anionic detergents were among the most effective activators of the enzymes, while cationic and nonionic detergents showed little and no effect on the PPO activities, respectively.     

Lipids of Hevea brasiliensis and Euphorbia coerulescens

The low MW lipids identified in the latices of Hevea brasiliensis and Euphorbia coerulescens were as follows: 2-methylcyclobutanone; 2-methyl-2-hydroxycyclobutanone; 2-methylcyclobutanol; euphol; euphorbol; and tirucallol.     

Composes halogenes d'une algue rouge,Falkenbergia rufolanosa tetrasporophyte d' Asparagopsis armata

Water extraction of fresh Falkenbergia rufolanosa followed by water-ether partition, yielded halomethanes, polyhalo ethyl and methyl acetates and especially polyhalo acetones. It is the first example of polyhalo compounds extracted from a tetrasporophyte in the Bonnemaisoniaceae.     

A role for a Hevea latex lectin-like protein in mediating rubber particle aggregation and latex coagulation

An in vitro aggregation of washed lutoid membrane and rubber particles, respectively, prepared from the bottom (lutoid) fraction and rubber layer of centrifuged fresh latex, leading to the formation of rubber coagulum necessary for a latex coagulation was demonstrated. A Triton X-100 extract of washed lutoid membrane proteins, isolated and prepared from the bottom fraction of centrifuged fresh latex was examined for its role in the latex coagulation process. It induced agglutination of rabbit erythrocytes, indicating the presence of a lectin-like protein. Hevea latex lectin-like protein (HLL) was purified to homogeneity by active chitin binding separation, followed by DEAE-Sepharose chromatography. Its M(r) analyzed by SDS-PAGE was 17 kDa, whereas that determined by gel filtration was 267 kDa. The HLL had a pI value of 7.2. Several glycoproteins were shown to inhibit the HLL-induced hemagglutination. The hemagglutinin activity of HLL was enhanced by Ca(2+). Of most interest was the finding that HLL strongly induced aggregation of the Hevea latex rubber particles (RP). This strong RP aggregation leads to latex coagulation, indicating the possibility that it is involved in the formation of the coagulum that plugs the latex vessel ends and stops the flow of latex upon tapping. In addition, the purified HLL also induced aggregation of RP taken from several other non-Hevea latex producing plants. This might indicate either a common or universal role of this lectin-like protein in RP aggregation and hence latex coagulation. This paper, for the first time, provides clear and unequivocal evidence for either a key biological role or physiological function of an endogenous latex lectin-like protein in the sequential process of latex coagulation.     

Diverses proprietes de l'absorption du citrate du malate et du succinate par les lutoides du latex d'Hevea brasiliensis

Lutoïds from Hevea latex are microvacuoles with lysosomal character. In vitro in a medium free of energetic substrate citrate, malate and succinate are absorbed. The properties of this absorption and the action of some modifiers are discussed.     

A rubber particle protein specific for Hevea latex lectin binding involved in latex coagulation

In the first of this three paper series, an in vitro latex coagulation was shown to arise from aggregation of rubber particles (RP) and lutoid membranes. RP aggregation was shown to be induced by a specific Hevea latex lectin-like protein (HLL) present on the lutoid membrane. In this second paper, a binding protein (BP) ligand counterpart for HLL was identified. This RP-HLLBP, having a specific interaction, with HLL was isolated from RP and characterized. The protein was extracted from the small RP in the presence of a surfactant (0.2% Triton-X-100) and further purified to homogeneity. Purification steps included acetone precipitation, heat-treatment, and column chromatography. The presence of RP-HLLBP was monitored by its ability to compete with erythrocytes in the hemagglutination inhibition (HI) assay. The purified RP-HLLBP had an HI titre of 1.37 microgml(-1), a pI value of 5.4, optimum activity at pH 5-8 and was thermostable up to 60 degrees C. On SDS-PAGE a single glycoprotein with M(r) of 24 kDa was detected while on native PAGE the major Mr was about 120 kDa. The purified RP-HLLBP was shown to inhibit latex coagulation. Chitinase, but no other glycosidase tested, abolished its HI action and inhibited HLL-induced RP aggregation in a competitive dose dependent manner. This indicated the presence of, and role for, N-acetylglucosamine residues in the binding recognition. The Hevea latex lectin-like protein can thus be referred to as a Hevea latex lectin. Based on protein identification by peptide mass fingerprinting, the RP-HLLBP was confirmed to be the small rubber particle protein (SRPP). This work has unambiguously determined the role of an intrinsic RP glycoprotein (RP-HLLBP or SRPP) as a key component in formation of the rubber latex coagulum.     

Physiological activators of invertase from Hevea brasiliensis latex

Potassium or sodium nitrates or phosphates, and thiols such as reduced glutathione or cysteine, stimulate the activity of invertase from Hevea brasiliensis latex. These activators raise the V_max but do not affect the K_m of the enzyme for sucrose. The action of these effectors is additive. Their efficiency is pH dependent, being higher below pH 7.0 and markedly decreasing above it.     

Hevains: Serine-centred proteases from the latex of Hevea brasiliensis

Hevains b and l, isolated respectively from the serum and lutoids of freeze-dried latex from Hevea brasiliensis, were purified to homogeneity and compared with hevain a from commercial, ammonia-treated latex. The M_rs of hevains a and b are 69 000 and 58 000, respectively, and both exist in several charged forms. The amino acid compositions of the two enzymes differ significantly, but the reactivities to a variety of ester and protein substrates are similar, as are the pH optima. Hevain l is a distinct protease of M_r 80 000 and unique amino acid composition. It displays esterolytic activity and will digest insulin B chain, but is not proteolytic to azocollagen, azocasein, bovine serum albumen or haemoglobin. The activities of all three enzymes are dependent on the presence of serine and histidine residues.     

Fatty acid composition and the characterization of a novel dioxo C18-fatty acid in the latex of Hevea brasiliensis

The fatty acids of the triacylglycerol fraction of the latex of the rubber plant consists of 97% of a C₁₈ furanoid fatty acid, 10,13-epoxy-11-methyloctadeca-10,12-dienoic. The free fatty acid fraction is composed of a more equally distributed mixture of 16:0, 18:0, 18:1, 18:2 and the furanoid acid. A novel dioxo fatty acid, 10,13-dioxo-11-methyloctadecanoic, was also isolated and characterized.     

Note preliminaire concernant la decouverte d'une faune et d'une flore du niveau de Ronzon dans l'Oligocene inferieur du Bassin d'Aquitaine

The new locality of Ruch (Gironde), from a lateral facies of the “Calcaire de Castillon” formation has yielded an important flora and fauna. From the biostratigraphic point of view the mammalian fauna allows to show that Ruch is contemporaneous of the reference locality of Ronzon (Auvergne).     

Modification of pH of latex cytoplasm by ethylene

In the absence of glycolytic activity the pH of isolated latex cytoplasm of Hevea brasiliensis increases progressively during the first hours of incubation. This increase is greatly enhanced after bark treatment with 2-chloroethylphosphonic acid. The process of alkalization is not enzymic and is oxygen dependent. This observation is discussed in relation to the increase in latex pH in situ under hormone action.     

Three serine proteases from the latex of Euphorbia cyparissias

Three serine-centred proteolytic enzymes, euphorbains y-1, ?2 and ?3, were isolated from the latex of Euphorbia cyparissias. These proteases have different specific activities to azocoll and CBZ glycine p-nitrophenyl ester. The pIs and M_rs of y-1, ?2 and ?3 are 5.2 and 67 000, 5.2 and 33 000, and 6.3 and 67 000, respectively. The enzymes, which are glycoproteins, are immunologically distinct from euphorbain 1, but clearly related to that enzyme in amino acid composition.     

ATPase membranaire de vacuoles lysosomales: Les lutoides du latex d'Hevea brasiliensis

Membranes of the lutoids present in the latex of Hevea brasiliensis possess an ATPase which is separable from adsorbed residual acid phosphatase. The pH optimum of the ATPase is 7.75 in Tris—HCl and is displaced to 6.5 in K-phosphate buffer. A divalent cation is obligatory (Mg  Mn > Ca). ATP-Mg is the natural substrate of the enzyme. Monovalent cations have practically no action on the enzyme. It is, however, activated by anions, both inorganic (Cl^?, HCO₃^?) and organic (malate, aspartate, tartrate). The enzyme has a higher specificity for ATP than for GTP, CTP or UTP and is non-competitively inhibited by ADP. The enzyme is temperature sensitive and a break in the Arrhenius plot occurs at about 20°, characteristic of membrane-bound enzymes. SH-group poisons inhibit enzyme activity as do classical uncouplers at high concentrations (about 10^?3 M). A hypothesis is formulated whereby the membrane-bound lutoid ATPase functions as a proton pump in order to maintain the acid pH of a vacuolar and lysosomal compartment.     

Fractionation of Hevea brasiliensis latex on ficoll density gradients

Fractionation of diluted Hevea brasiliensis latex on iso-osmotic Ficoll density gradients by sedimentation produces a sharp acid phosphatase-rich lutoid band at the density of ca1.04 g/cm³. Polyphenol oxidase (PPO) is not exclusively located in the Frey-Wyssling complexes as shown earlier by others; its distribution is variable. A complete separation of acid phosphatase and PPO activities can be obtained by flotation in a Ficoll density gradient. Ethephon stimulation of the tree reduces the acid phosphatase and PPO activities. A transient change in lutoid density soon after stimulation is observed. The occurrence of some new enzyme activities and their subcellular localization are reported.     

Produits d'alteration thermooxydative des huiles chauffees. II: Composes apolaires ou faiblement polaires

Non-polar or slightly polar compounds formed as a consequence of thermal or oxidative reactions, during heating of oils in deep fat frying conditions, have been isolated by chromatographic fractionation of the methyl esters.These compounds are esters of monomeric cyclic or aromatic fatty acids, tetrasubstituted cyclohexenic diacids, disubstituted αω diacids, estolides, disubstituted αω diacids with an ether bridge, and tetrasubstituted hydrofuranic diacids.Most of these new compounds are the results of reactions between dienoic and in some case trienoic acids.     

Hydroxymethylglutaryl coA reductase (NADPH) in the latex of Hevea brasiliensis

The activity of hydroxymethylglutaryl CoA reductase (NADPH) (EC 1.1.1.34) was studied in the latex of regularly tapped mature trees of Hevea brasiliensis. The reductase activity was found mainly (95% of the total activity) in the pellet fraction (40 000 g) of the centrifuged latex. The enzyme in this fraction had a specific requirement for NADPH as the cofactor and, while not obligatory for activity, was activated by dithiothreitol at the optimum concentration of 2 mM. The pH optimum was found to be 6.6–6.9 in 0.1 M phosphate buffer. Mevalonate and CoA (at 2 mM each) did not affect enzyme activity, while hydroxymethylglutarate (2 mM) was slightly inhibitory. p-Chloromercuribenzoate (1 mM) completely inhibited this enzyme. The reductase activity in the 40 000 g pellet was not easily solubilized either using Triton X-100 or by sonication. The apparent K_m for the washed, membrane-bound enzyme (103 000 g pellet) was 56 μ M (RS-HMG-CoA). Magnesium-ATP (4 mM) inactivated the reductase but this effect was greatly diminished or was absent upon washing the 40 000 g pellet.     

Hevein: an antifungal protein from rubber-tree (Hevea brasiliensis) latex

Several chitin-binding proteins were isolated from the bottom fraction of Hevea brasiliensis (Müll.) Arg. latex. One of these chitin-binding proteins is hevein, a small monomeric protein which strongly resembles the lectin from stinging nettle (Urtica dioica L.). Like the latter, hevein showed strong antifungal activity against several fungi in vitro. The possible involvement of this protein in the defense against invasion by potentially pathogenic fungi is discussed.Abbreviations FPLC fast protein liquid chromatography - M_r apparent molecular mass - SDS-PAGE Sodium dodecyl sulp-hatepolyacrylamide gel electrophoresis - UDA Urtica dioica agglutinin - WGA Wheat-germ agglutinin This work is supported in part by NIH grant and grants of the National Fund for Scientific Research (Belgium): W.J.P. is senior research associate, and W.F.B. senior research assistant of this fund. J.V.P. receives a fellowship of the Belgian Instituut tot Aanmoediging van het Wetenschappelijk Onderzoek in Nijverheid en Landbouw.