Characterization of NADH-dependent Fe3+-chelate reductases of maize roots

Iron-deficient maize seedlings exhibit a starvation syndromecharacterized by an increase in different parameters such asroot fresh weight (+ 30%), protein (+ 25%) and plasma membrane-associatedNADH Fe³⁺ –EDTA reductase (NFR; +45%). NFR activity wasfound associated with 9 000g (20 min) and 110 000 g (1 h) sediments,purified plasma membrane and 110000 g supernatants. No differenceswere observed between the properties of reductases from Fe-starvedversus Fe-sufficient roots. The characterization of NFR wasundertaken. Low Mr forms (46 and 28 kDa, as detected by size-exclusionchromatography) were present in all fractions whereas 210 and110 kDa forms were unique in membranes and 110 000 g supernatants,respectively. The 210 kDa form was solubilized from microsomes and characterized.The enzyme is cetone-resistant and appears to be comprised largelyif not totally of the low Mr forms (46 and 28 kDa, correspondingto 30 and 32 kDa bands, respectively, in SDS-PAGE). The 210kDa form tended to break down to subunits following dilution,and the effect could be prevented by addition of 10% (v/v) glycerol.A three-step purification procedure for microsomal NFR was devised,consisting of acetone fractionation of lysophosphatidycholinesolubilized microsomes, Blue Sepharose CL-6B affinity chromatographyand a final size exclusion chromatography in the absence ofdetergent, resulting in a 700-fold purification of the 28 kDaprotein. The best electron acceptor for the purified 28 kDaform was ferricyanide (400µmol min^–1mg^–1 protein)followed by Fe³⁺–chelates (up to 200µol min^–1mg^–1 protein) and other compounds to a lesser extent (cytc, DCPIP).The 46 kDa form, on the other hand, had high ferricyanidereductase activity (about 300µmol min^–1mg^–1protein) and relatively low Fe³⁺–chelate reductase activity.The properties of NFR (high M, active forms, donor and acceptorspecificity, purification behaviour, large hydrophilic domains,size of subunits) suggest a relationship with the NADH-cyt b5reductase family of FAD-containing proteins. None of the latterflavoproteins is a transmembrane enzyme. Key words: Maize roots, Fe³⁺–reductase, ferricyanide reductase, iron     

Partial Purification of a Soluble Gibberellin-Binding Protein from Mung Bean Hypocotyls

A soluble binding protein specific for GA₄, GA₇ and GA₉ waspartially purified from mung bean hypocotyls, and its characteristicswere examined. Affinity chromatography using immobilized GA₃coupled to Sepharose 4B via the C-7 carboxyl group was veryeffective for purification of the protein. The molecular weightof the protein in its native state was estimated to be 150–200kDa by gel-permeation chromatography. This protein may be aheterooligomer consisting of two subunits (23 kDa and 35 kDa).The optimum pH for binding of GA₄ to the protein was around6.0 and the apparent dissociation constant (K_d) was 310^-7 M. (Received April 24, 1992; Accepted December 16, 1992)     

Partial Purification and Characterization of An ATPase in Mung Bean Hypocotyl Plasma Membrane: Suggestion for A New Type of Higher Plant Plasma Membrane ATPase

A vanadate-sensitive and nitrate-resistant ATPase was solubilizedwith Zwittergent 3–14 from a highly purified plasma membranefraction of mung bean hypocotyls and partially purified by glyceroldensity gradient centrifugation and phenyl-Sepharose columnchromatography. Either phosphatidylcholine or phosphatidylserinein addition to Mg^{2 +} was required for the enzyme activity, whereasK⁺, phosphatidylethanolamine and lysophosphatidylcholine hadno effect on the activity. The purified enzyme preparation containedtwo major polypeptides with molecular masses of 67 and 55 kDaas analyzed by SDS-polyacrylamide gel electrophoresis. Whenthe plasma membrane fraction was incubated with [-³²P]ATP, a45-70-kDa polypeptide(s) was labeled, and the label could berapidly chased with cold ATP. When the fraction was incubatedwith [¹⁴C]N,N'-dicyclohexylcarbodiimide, an inhibitor for theATPase, a 15-20-kDa polypeptide was labeled. We propose thatthe enzyme is a new type of higher plant plasma membrane ATP-aseand is composed of 67- and 55-kDa subunits and probably alsoa 15-20-kDa subunit. ¹Present address: Takarazuka Institute, Sumitomo Chemical IndustriesLtd., Takatsukasa, Takarazuka, Hyogo 665, Japan (Received September 2, 1987; Accepted May 20, 1988)     

Proteins and Carbohydrates in Xylem Sap from Squash Root

The xylem sap from squash roots was collected from the cut surfaceof stems, and the proteins and carbohydrates in the sap wereanalyzed. The sap contained 18.6 µg ml^–1 proteinand the major polypeptides were as follows: 1) two polypeptides,of 75 and 40 kDa, with high-mannose glycans, the levels of whichincreased for about 24 h after cutting and then decreased; 2)a 32-kDa polypeptide, which appeared soon after cutting, disappearedand then reappeared again 48–64 h after cutting; and 3)a 19-kDa and a 14-kDa polypeptide, which were present constitutively.The carbohydrates contained in the xylem sap were fractionatedinto 80% ethanol-soluble and -insoluble material, and whichwere analyzed by high-performance liquid chromatography, gaschromatography and enzymatic mathods. The former fraction containedconsiderable amounts of myo-inositol and fructose as free sugarsand oligosaccharides composed mainly of galactose, arabinoseand glucose. The latter contained polysaccharides composed mainlyof uronic acids, galactose and arabinose. The possible significanceof these substances, which may mediate the interactions betweenthe root and the aerial organs, is discussed. (Received April 20, 1992; Accepted July 4, 1992)     

Effects of Growth Regulators and Glutamine on In Vitro Development of Zygotic Embryos of Taro (Colocasia esculenta var. antiquorum)

Zygotic embryos of taro, Colocasia esculenta var. antiquorumcultured on Linsmaier-Skoog (LS) medium without the additionof hormones develop into mature plants only in the presenceof endosperm tissue. Growth is usually evident within the firstweek of culture when embryos swell and become green. Embryosexcised from endosperm and cultured on LS containing 0-01 mg1^–1 naphthaleneacetic acid (NAA), and 0–01 mg 1^–16-dimethylaminopurine (6-DMAP) grow at a rate comparable withcontrols for the first week of culture. During the second week,growth rates are higher than controls primarily because embryosform elongated hypocotyl regions which often produce swollentissues and/or callus. In the presence of 200 mg 1^–1 glutamineand a range of concentrations of 6-dimethylaminopurine, benzyladenine,or NAA, elongation of the hypocotyl axis is inhibited, and acompact callus may develop. Embryos grown on LS containing 200mg 1^–1 glutamine and 2.0 mg 1^–1 2, 4, 5-trichlorophenoxyaceticacid form friable callus which was used to generate short-livedsuspension cultures. Growth Regulators, Glutamine, tygotic embryos, Colocasia esculenta, endosperm     

Response of Glutamine Synthetase and Glutamate Synthase Isoforms to Nitrogen Sources in Rice Cell Cultures

As a model system with no photorespiration and no long distancetransport, rice cell cultures (Oryza saliva L. cv Sasanishiki)were used to investigate the effect of nitrogen sources on thelevels of isoforms of glutamine synthetase (GS) and glutamatesynthase (GOGAT). Isoforms of GS and GOGAT were analyzed byimmunoblotting methods and their activities in early growthphase of the cells. Cytosolic type GS (41 kDa subunit) and NADH-GOGATwere the major isoforms in the rice cells grown in normal R-2medium. However, contents of plastid type GS (44 kDa subunit)and Fd-GOGAT increased in response to NO_–³ supply. NADH-GOGATactivity also increased following the supply of NO_–³.In vitro translated products from poly(A)⁺RNA prepared fromthe cells showed that the precursor of plastid type GS (49 kDa)was detected at 48 h after the inoculation. Supply of NH₊⁴ resultedin an increase in NADH-GOGAT activity but had no effect on thelevels of Fd-GOGAT, of polypeptides of the plastid type GS orof the corresponding mRNAs. (Received May 30, 1990; Accepted August 23, 1990)     

The COOH termini of NBC3 and the 56-kDa H+-ATPase subunit are PDZ motifs involved in their interaction

The electroneutralsodium bicarbonate cotransporter 3 (NBC3) coimmunoprecipitates fromrenal lysates with the vacuolar H⁺-ATPase. In renal type Aand B intercalated cells, NBC3 colocalizes with the vacuolarH⁺-ATPase. The involvement of the COOH termini of NBC3 andthe 56-kDa subunit of the proton pump in the interaction of theseproteins was investigated. The intact and modified COOH termini of NBC3 and the 56-kDa subunit of the proton pump were synthesized, coupled toSepharose beads, and used to pull down kidney membrane proteins. Boththe 56- and the 70-kDa subunits of the proton pump, as well as a PDZdomain containing protein Na⁺/H⁺ exchangerregulatory factor 1 (NHERF-1), were bound to the intact 18 amino acidNBC3 COOH terminus. A peptide truncated by five COOH-terminal aminoacids did not bind these proteins. Replacement of the COOH-terminalleucine with glycine blocked binding of both the proton pump subunitsbut did not affect binding of NHERF-1. The 18 amino acid COOH terminusof the 56-kDa subunit of the proton pump bound NHERF-1 and NBC3, butthe truncated and modified peptide did not. A complex of NBC3, the56-kDa subunit of the proton pump, and NHERF-1 was identified in ratkidney. The data indicate that the COOH termini of NBC3 and the 56-kDasubunit of the vacuolar proton pump are PDZ-interacting motifs that arenecessary for the interaction of these proteins. NHERF-1 is involved inthe interaction of NBC3 and the vacuolar proton pump.

     

The head structure of a higher plant V-type H+-ATPase is not always a hexamer but also a pentamer

Pentameric head structures of the V-type H⁺–ATPase ofMesembryanthemum crystallinum L. were demonstrated in additionto hexameric head structures by rotational image analysis andmolecular projections of negatively stained H⁺–ATPaseheads. This observation, at least partially, is in contrastto the standard model of the V-type H⁺–ATPase predictingsolely a hexameric head structure with three A and three B subunitsin analogy to the F-type ATPases. With one A or B subunit missingtwo A or two B subunits would be adjacent to each other in thepentameric ATPase head. By chemical cross-linking of H ⁺–ATPasesubunits a crosslinking product exclusively consisting of Bsubunits, in addition to a cross-linking product consistingof subunits A and B was detected. Thus, the pentameric headsmight lack one A subunit, although the lack of one B subunitcan not be totally ruled out. We assume that the hexameric headstructure is the catalytically active configuration while thepentameric head structure may be a relatively stable intermediateof turnover. Key words: V-type H⁺–ATPase, protein structure, electron microscopy, tonoplast, Mesembryanthemum crystallinum L     

Accumulation and Conversion of Sugars by Developing Wheat Grains: V. THE ENDOSPERM APOPLAST AND APOPLASTIC TRANSPORT

The volume and composition of the endosperm apoplast of thedeveloping wheat grain, comprising endosperm cavity and intercellularfree-space, was examined in relation to kernel growth rate andsize. Samples of the cavity sap were collected by centrifugationof kernels during the linear phase of grain growth. The cavitysap contained 10–50 mM sucrose, a small amount of hexosesbut a high concentration of oligosaccharides (up to 9 timesthat of sucrose). In comparing cvs Yandilla King and Cleveland,high growth rate was associated with high cavity sap sucroseconcentration but with low K⁺ concentration. K⁺ concentrationin the endosperm cells (124 mM) was about 5 times higher thanin the cavity sap (10–40 mM). Cavity sap pH was 6.3–6.6.The uptake of sucrose by endosperm cells was partly inhibitedby PCMBS, an inhibitor of membrane-bound carriers. Several necessaryconditions for proton cotransport during sucrose uptake by endospermcells were met. The volume of the intercellular free-space, estimated by membranepermeating (¹⁴C-mannitol, ¹⁴C-sucrose) or non-permeating (³H-PEG900)markers averaged 2.2 µl or 5–7% of the water ingrains of cvs Yandilla King, Cleveland and SUN 9E. The cavityvolume was highly variable but tended to be larger in largergrains. Pulse labelling of ¹⁴CO₂ to flag leaves showed that ¹⁴C-sucrosewas the principal ¹⁴C-assimilate in the cavity sap and was convertedto insoluble compounds in the endosperm while the cavity sapoligosaccharides acquired negligible label in 6 h. Key words: Wheat, Endosperm apoplast, Sugars     

Specific interaction of cytokinin binding protein with 40S ribosomal subunits in the presence of cytokinin in vitro

Cytokinin binding protein (CB-protein) prepared from tobacco(Nicotiana tabacum var. Bright Yellow) leaves by affinity chromatographywas found to bind specifically to 40S ribosomal subunits butnot to 60S subunits in vitro at 37?C. The binding capacity to0.5 M KCl-washed ribosomes was about 10 times higher than thatto unwashed ribosomes, stimulated 3 times by a synthetic cytokinin,benzyladenine, and was completely inhibited by 0.4 M KCl. Underoptimum conditions, 2 to 3 moles of CB-protein bound to oneKCl-washed ribosomal subunit. About 80–70, 10–8, 8–4, 6 and 3% of totalCB-protein were present in supernatant, ribosomal, mitochondrial,chloroplast and nuclear fractions, respectively. A considerableamount of CB-protein was isolated from KCl-wash of ribosomeswhich is believed to contain the initiation factors for proteinsynthesis. The roles of CB-protein in protein synthesis arediscussed. ¹ Present address: Tokyo Metropolitan Institute for Neurosciences,2–6 Musashidai, Fuchu-City, Tokyo, Japan. (Received September 22, 1976; )     

Structural characterization of heterodimeric laccases from <Emphasis Type="Italic">Pleurotus ostreatus</Emphasis>

The subfamily of POXA3 laccase isoenzymes produced by the fungus Pleurotus ostreatus has been characterized as an example of the complexity and heterogeneity of fungal isoenzyme patterns. Two isoenzymes, POXA3a and POXA3b, were previously purified, exhibiting an unusual heterodimeric structure composed of a large (67 kDa) and a small (18 or 16 kDa) subunit. A unique gene encodes the large subunit of both POXA3a and POXA3b, but alternative splicing produces two variants—differing for an insertion of four amino acids—for each isoenzyme. Two genes encoding POXA3a and POXA3b small subunits have been identified, and the corresponding amino acid sequences show only two amino acid substitutions. The 18- and 16-kDa subunits of both POXA3a and POXA3b differ for N-glycosylation at Asn150 of the 16-kDa subunit. The POXA3 large subunit 3D model allows us to highlight peculiarities of this molecule with respect to the laccases whose 3D structures are known.     

The Large Subunit of Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase is Fragmented into 37-kDa and 16-kDa Polypeptides by Active Oxygen in the Lysates of Chloroplasts from Primary Leaves of Wheat

Lysates of chloroplasts isolated from wheat (Triticum aestivumL. cv. Aoba) leaves were incubated on ice (pH 5.7) for 0 to60 min in light (15 µmol quanta m^–2 s^–1),and degradation of the large subunit (LSU) of ribulose-l,5-bis-phosphatecarboxylase/oxygenase (Rubisco: EC 4.1.1.39 [EC] ) was analyzed byapplying immunoblotting with site-specific antibodies againstthe N-terminal, internal, and C-terminal amino acid sequencesof the LSU of wheat Rubisco. The most dominant product of thebreakdown of the LSU and that which was first to appear wasan apparent molecular mass of 37-kDa fragment containing theN-terminal region of the LSU. A 16-kDa fragment containing theC-terminal region of the LSU was concomitantly seen. This fragmentationof the LSU was inhibited in the presence of EDTA or 1,10-phenanthroline.The addition of active oxygen scavengers, catalase (for H₂O₂)and n-propyl gallate (for hydroxyl radical) to the lysates alsoinhibited the fragmentation. When the purified Rubisco fromwheat leaves was exposed to a hydroxyl radical-generating systemcomprising H₂O₂, FeSO₄ and ascorbic acid, the LSU was degradedin the same manner as observed in the chloroplast lysates. Theresults suggest that the large subunit of Rubisco was directlydegraded to the 37-kDa fragment containing the N-terminal regionand the 16-kDa fragment containing the C-terminal region ofthe LSU by active oxygen, probably the hydroxyl radical, generatedin the lysates of chloroplasts. (Received October 28, 1996; Accepted February 7, 1997)     

Roles of Sucrose-Metabolizing Enzymes in Growth of Seedlings. Purification of Acid Invertase from Growing Hypocotyls of Mung Bean Seedlings

Changes in activities of acid invertase and sucrose synthaseduring growth of mung bean seedlings were examined and the correlationbetween the activity of acid invertase and growth was confirmed.Acid invertase was purified from hypocotyls of etiolated seedlingsand separated into two fractions (A and B) by chromatographyon hydroxylapatite. Acid invertase in fraction B consisted oftwo polypeptides of 30 kDa and 38 kDa, but that in fractionA was 70 kDa in size. Antibodies raised against the 30-kDa polypeptideimmunoprecipitated enzymatic activity but those raised againstthe 38-kDa polypeptide did not. The concanavalin A-binding siteof acid invertase was contained in the 38-kDa polypeptide andnot in the 30-kDa polypeptide. However, when acid invertasewas bound to and eluted from concanavalin A-Sepharose, the 30-kDapolypeptide was found together with the 38-kDa polypeptide inthe eluate. Acid invertase in hypocotyls of mung bean seedlingsappears to be present in two forms: a monomer of 70 kDa anda hetero-dimer of 30-kDa and 38-kDa polypeptides. The monomerwas not converted to the heterodimer during incubation of acrude extract and was present together with the heterodimerin very young hypocotyls. In older hypocotyls, the heterodimerwas present but the monomer was barely detectable. We concludethat the two forms of acid invertase are present within cells,but the relationship between the two forms is unknown at present. (Received July 18, 1991; Accepted October 9, 1991)     

Post-transcriptional regulation of protein synthesis during alfalfa embryogenesis: proteins associated with the cytoplasmic polysomal and non-polysomal mRNAs (messenger ribonucleoprotein complex)

Cytoplasmic polysomal and non-polysomal mRNA-associated proteincomplexes were isolated from, and characterized in, developingsomatic and zygotic embryos of alfalfa (Medicago sativa L.).³⁵S-methionine-labelled intact embryos were irradiated withultraviolet light (UV) in situ to cross-link mRNA and proteinsoccurring within one bond length, and the polysomal and non-polysomalfractions were extracted. Then the mRNA-protein complexes wereisolated from the fractions and separated using two cycles ofaffinity chromatography on an oligo(dT)-cellulose column. Followingdigestion with RNase A and T1 and micrococcal nuclease, mRNA-associatedproteins were separated by SDS-PAGE. Several polypeptides of 15–150 kDa were associated withthe polysomal and non-polysomal (ribonucleoprotein, mRNP) fractionsof alfalfa embryos after UV-cross-linking. Many of the polypeptidesassociated with the polysomal and non-polysomal mRNAs were qualitativelysimilar, although their concentration in the two fractions wasdifferent. However, some developmentally stage-specific polypeptideswere found to be associated with the non-polysomal mRNA fractionduring the early stages of embryogenesis (precotyledonary) ofsomatic embryos. Thus the presence of mRNPs during embryogenesishas been demonstrated, and proteins intimately associated withthe mRNAs identified. Key words: Embryogenesis, translational control, protein synthesis, messenger ribonucleoproteins, alfalfa (Medicago sativa L.)     

Molecular evolution of ribulose-1, 5-bisphosphate carboxylase

The structural homology of the two constituent subunits (A andB) of ribulose- 1,5-bisphosphate carboxylase from various originswas determined using the statistical method of Marchalonis andWeltman [Comp. Biochem. Biophys. 38B, 609–625 (1971)].It was found that the large catalytic subunit (A) is structurallyhomologous among the enzymes of divergent origins, from primitivephotosynthetic bacteria (Bacteriophyta) through the green algae(Chlorophyta) to higher plants (Tracheophyta). In contrast,the small regulatory subunit (B) was found to be structurallyquite different among the different species. The genetic conservationof subunit A during the phylogenetic evolution of the ribulose-1,5-bisphosphatecarboxylase molecule indicates its origin from a common ancestralgene. ¹ This is paper XXXIII in the series "Structure and Functionof Chloroplast Proteins". (Received July 23, 1975; )     

Freezing Tolerance in Hydrated Lactuca sativa (L) Seed: A Model to Explain Observed Variation Between Seed Lots

Low temperature tolerance was investigated in the imbibed seedof 15 seed lots compnsmg seven cultivars of Lactuca sativa L.During rapid cooling (20 °C h^–1) some seeds of allseed lots survived to –16 °C but none to –20°C. The majority of seed lots retained over 50 per centviability above –14 °C due to isolation of the embryofrom external ice by the endosperm, and subsequent embryo super-cooling.Certain seed lots, including all three seed lots of cv. TomThumb, showed high mortality at temperatures above –10°C. Correlation of mortality with the formation of externalice suggested that the endosperm is not an effective nucleationbarrier in these seed lots. Survival to –20 °C was increased at slower coolingrates (6 to 1 °C h^–1) due to freeze desiccation ofthe embryo, but seed lots varied considerably in their toleranceof specific cooling rates. A model to explain this variationwas developed incorporatmg (1) seed lot super-cooling limittemperature, (2) the rate at which freeze dehydration of thesupercooled embryo took place, (3) the moisture content at whichnucleation (at –20 °C) was no longer certain and (4)the.initial equilibrium moisture content of the fully imbibedseed. Factors (1), (2) and (3) were found to be relatively constant,but low (or artificially reduced) seed moisture content wasclosely correlated with high survival at natural cooling rates.Seed size fractions of similar moisture content from a singlecultivar showed that more small seeds survive cooling at 3 °Ch^–1 to –20 °C than larger seed. Seed with pierced endosperms or ineffective nucleation barrierswere capable of surviving to at least –10 °C if cooledslowly (1 °C h^–1) but were killed by rapid (20 °Ch^–1) cooling. Lactuca sativa L, lettuce, seed germination freezing tolerance, super-cooling     

Purification of a Dithiothreitol-Sensitive Tetrameric Protease from Spinach PS II Membranes

A protease with a tetrameric quaternary structure was extractedwith 1 M NaCl from spinach PS II membranes and purified by hydrophobic,anion-exchange and gel-filtration chromatography using onlybuffers of high ionic strength. Gel-filtration chromatographyresulted in elution of the protease in fractions that correspondedto molecular masses of 156 kDa and 39 kDa, and re-chromatographyof either peak gave both peaks again. This result indicatesthat the protease is represented by an equilibrium between a156-kDa tetramer and a 39-kDa monomer. SDS-polyacrylamide gelelectrophoresis of the protease fractions revealed a polypeptidewhose molecular mass was 39 kDa without prior reduction, butthe molecular mass increased to 41 kDa after prior reductionwith dithiothreitol. This finding suggests that the monomerpossesses an intramolecular disulfide linkage whose reductioncauses a configurational change that increases the effectivemolecular size. The protease had maximum activity at pH 7.0–9.0.The activity was diminished by the presence of 5 mM NaCl andwas almost completely inhibited by 50 mM NaCl. These observationssuggest that an environment of low ionic strength is a prerequisitefor the activity of this enzyme. The protease was inhibitedby dithiothreitol, a result that indicates that the 39-kDa formmaintained by the disulfide linkage is essential for activity.Studies with protease inhibitors suggested that this enzymeis not a serine-protease. ¹Present address: Department of Biomolecular Science, Facultyof Science, Toho University, Miyama 2-2-1, Funabashi, 274 Japan (Received October 19, 1989; Accepted April 12, 1990)     

Distribution of Indole-3-Acetic Acid in the Apoplast and Symplast of Squash (Cucurbita maxima) Hypocotyls

The concentration of endogenous IAA was higher in an apoplasticsolution (2.3xl0^–7M) than in a symplastic solution (0.5x 10^–7 M) obtained from segments of etiolated squash (Cucurbitamaxima Duch.) hypocotyls. Exogenously applied IAA (10^–5M) increased the level of IAA in both the apoplastic and thesymplastic solution. The concentration of IAA in the apoplasticsolution increased to 75% of the concentration of exogenousIAA in 4 h, but that in the symplastic solution increased onlyto 23% of the concentration of exogenous IAA. These resultsdemonstrate that the concentration of endogenous IAA is higherin the apoplast than in the symplast of squash hypocotyls, andthey suggest that IAA exerts its physiological effects, at leastto some extent, from the outside of cells. (Received September 20, 1996; Accepted January 10, 1997)