Plant Physiology

Drobak, B. K.

doi: 10.1104/pp.102.3.705pmid: 12231858

Article PDF first page preview Close This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Kearns, E. V.; Assmann, S. M.

doi: 10.1104/pp.102.3.711pmid: 12231859

Article PDF first page preview Close This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Yang, T.; Law, D. M.; Davies, P. J.

doi: 10.1104/pp.102.3.717pmid: 12231860

Abstract Exogenously applied indole-3-acetic acid (IAA) strongly promoted stem elongation over the long term in intact light-grown seedlings of both dwarf (cv Progress No. 9) and tall (cv Alaska) peas (Pisum sativum L.), with the relative promotion being far greater in dwarf plants. In dwarf seedlings, solutions of IAA (between 10–)4 and 10–)3 M), when continuously applied to the uppermost two internodes via a cotton wick, increased whole-stem growth by at least 6-fold over the first 24 h. The magnitude of growth promotion correlated with the applied IAA concentration from 10–)6 to 10–)3 M, particularly over the first 6 h of application. IAA applied only to the apical bud or the uppermost internode of the seedling stimulated a biphasic growth response in the uppermost internode and the immediately lower internode, with the response in the latter being greatly delayed. This demonstrates that exogenous IAA effectively promotes growth as it is transported through intact stems. IAA withdrawal and reapplication at various times enabled the separation of the initial growth response (IGR) and prolonged growth response (PGR) induced by auxin. The IGR was inducible by at least 1 order of magnitude lower IAA concentrations than the PGR, suggesting that the process underlying the IGR is more sensitive to auxin induction. In contrast to the magnitude of the IAA effect in dwarf seedlings, applied IAA only doubled the growth in tall seedlings. These results suggest that endogenous IAA is more growth limiting in dwarf plants than in tall plants, and that auxin promotes stem elongation in the intact plant probably by the same mechanism of action as in isolated stem segments. However, since dwarf plants to which IAA was applied failed to reach the growth rate of tall plants, auxin cannot be the only limiting factor for stem growth in peas. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Hugdahl, J. D.; Morejohn, L. C.

doi: 10.1104/pp.102.3.725pmid: 12231861

Abstract Oryzalin, a dinitroaniline herbicide, was previously reported to bind to plant tubulin with a moderate strengthe interaction (dissociation constant [Kd] = 8.4 [mu]M) that appeared inconsistent with the nanomolar concentrations of drug that cause the loss of microtubules, inhibit mitosis, and produce herbicidal effects in plants (L.C. Morejohn, T.E. Bureau, J. Mole-Bajer, A.S. Bajer, D.E. Fosket [1987] Planta 172: 252–)264). To characterize further the mechanism of action of oryzalin, both kinetic and quasi-equilibrium ligand-binding methods were used to examine the interaction of [14C]-oryzalin with tubulin from cultured cells of maize (Zea mays L. cv Black Mexican Sweet). Oryzalin binds to maize tubulin dimer via a rapid and pH-dependent interaction to form a tubulin-oryzalin complex. Both the tubulin-oryzalin binding strength and stoichiometry are underestimated substantially when measured by kinetic binding methods, because the tubulin-oryzalin complex dissociates rapidly into unliganded tubulin and free oryzalin. Also, an uncharacterized factor(s) that is co-isolated with maize tubulin was found to noncompetitively inhibit oryzalin binding to the dimer. Quasi-equilibrium binding measurements of the tubulin-oryzalin complex using purified maize dimer afforded a Kd of 95 nM (pH 6.9; 23[deg]C) and an estimated maximum molar binding stoichiometry of 0.5. No binding of oryzalin to pure bovine brain tubulin was detected by equilibrium dialysis, and oryzalin has no discernible effect on microtubules in mouse 3T3 fibroblasts, indicating an absence of the oryzalin-binding site on mammalian tubulin. Oryzalin binds to pure taxol-stabilized maize microtubules in a polymer mass- and number-dependent manner, although polymerized tubulin has a much lower oryzalin-binding capacity than unpolymerized tubulin. Much more oryzalin is incorporated into polyment during taxol-induced assembly of pure maize tubulin, and half-maximal inhibition of the rapid phase of taxol-induced polymerization of 5 [mu]M tubulin is obtained with 700 [mu]M oryzalin. The data are consistent with a molecular mechanism whereby oryzalin binds rapidly, reversibly, and with high affinity to the plant tubulin dimer to form a tubulin-oryzalin complex that, at concentrations substoichiometric to tubulin, copolymerizes with unliganded tubulin and slows further assembly. Because half-maximal inhibition of maize callus growth is produced by 37 nM oryzalin, the herbicidal effects of oryzalin appear to result from a substoichiometric poisoning of microtubules. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Ruban, A. V.; Young, A. J.; Horton, P.

doi: 10.1104/pp.102.3.741pmid: 12231862

Abstract Simultaneous measurements of nonphotochemical quenching of chlorophyll fluorescence and absorbance changes in the 400- to 560-nm region have been made following illumination of dark-adapted leaves of the epiphytic bromeliad Guzmania monostachia. During the first illumination, an absorbance change at 505 nm occurred with a half-time of 45 s as the leaf zeaxanthin content rose to 14% of total leaf carotenoid. Selective light scattering at 535 nm occurred with a half-time of 30 s. During a second illumination, following a 5-min dark period, quenching and the 535-nm absorbance change occurred more rapidly, reaching a maximum extent within 30 s. Nonphotochemical quenching of chlorophyll fluorescence was found to be linearly correlated to the 535-nm absorbance change throughout. Examination of the spectra of chlorophyll fluorescence emission at 77 K for leaves sampled at intervals during this regime showed selective quenching in the light-harvesting complexes of photosystem II (LHCII). The quenching spectrum of the reversible component of quenching had a maximum at 700 nm, indicating quenching in aggregated LHCII, whereas the irreversible component represented a quenching of 680-nm fluorescence from unaggregated LHCII. It is suggested that this latter process, which is associated with the 505-nm absorbance change and zeaxanthin formation, is indicating a change in state of the LHCII complexes that is necessary to amplify or activate reversible pH-dependent energy dissipation, which is monitored by the 535-nm absorbance change. Both of the major forms of nonphotochemical energy dissipation in vivo are therefore part of the same physiological photoprotective process and both result from alterations in the LHCII system. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Getz, H. P.; Grosclaude, J.; Kurkdjian, A.; Lelievre, F.; Maretzki, A.; Guern, J.

doi: 10.1104/pp.102.3.751pmid: 12231863

Abstract Monoclonal antibodies were raised in mice against a highly purified tonoplast fraction from isolated red beet (Beta vulgaris L. ssp. conditiva) root vacuoles. Positive hybridoma clones and sub-clones were identified by prescreening using an enzyme-linked immunosorbent assay (ELISA) and by postscreening using a functional assay. This functional assay consisted of testing the impact of hybridoma supernatants and antibody-containing ascites fluids on basal and ATP-stimulated sugar uptake in vacuoles, isolated from protoplasts, as well as in tonoplast vesicles, prepared from tissue homogenates of red beet roots. Antibodies from four clones were particularly positive in ELISAs and they inhibited sucrose uptake significantly. These antibodies were specific inhibitors of sucrose transport, but they exhibited relatively low membrane and species specificity since uptake into red beet root protoplasts and sugarcane tonoplast vesicles was inhibited as well. Fast protein liquid chromatography assisted size exclusion chromatography on Superose 6 columns yielded two major peaks in the 55 to 65-kD regions and in the 110- to 130-kD regions of solubilized proteins from red beet root tonoplasts, which reacted positively in immunoglobulin-M(IgM)-specific ELISAs with anti-sugarcane tonoplast monoclonal IgM antibodies. Only reconstituted proteoliposomes containing polypeptides from the 55- to 65-kD band took up [14C]-sucrose with linear rates for 2 min, suggesting that this fraction contains the tonoplast sucrose carrier. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Chapman, K. D.; Moore Jr, T. S.

doi: 10.1104/pp.102.3.761pmid: 12231864

Abstract We recently demonstrated that cotyledons of cotton (Gossypium hirsutum L.) seedlings synthesize N-acylphosphatidylethanolamine (NAPE), an unusual acylated derivative of phosphatidylethanolamine (PE), during postgerminative growth (K.D. Chapman and T.S. Moore [1993] Arch Biochem Biophys 301: 21–)33). Here, we report the discovery of an acyltransferase enzyme, fatty acid: diacylphosphatidylethanolamine N-acyltransferase (designated NAPE synthase), that synthesizes NAPE from PE and free fatty acids (FFA) in cottonseed microsomes. [14C]NAPE was synthesized from [14C]palmitic acid and endogenous PE in a time-, pH-, temperature-, and protein concentration-dependent manner. [14C]Palmitic acid was incorporated exclusively into the N-acyl position of NAPE. [14C]palmitoyl coenzyme A (CoA) and [14C]-dipalmitoyl phosphatidylcholine (PC) were poor acyl donors for the synthesis of NAPE (i.e. 200- and 3000-fold lower incorporation efficiency than palmitic acid, respectively). Synthesis of NAPE from palmitoyl-CoA and dipalmitoyl-PC was observed only after the release of FFA in microsomes. We observed a temperature optimum of 45[deg]C and a pH optimum of 8.0 for the synthesis of [14C]NAPE from [14C]palmitic acid (or from [14C]PE). NAPE synthase activity showed no apparent divalent cation requirement. Notably, activity was stimulated by HPO42-, HCO3-, SO42-, and NADPH, whereas activity was inhibited by Ca2+, Mn2+, Cd2+, ATP, ADP, flavin adenine disnucleotide, and flavin mononucleotide. Other nucleotide triphosphates (GTP and CTP) and pyridine dinucleotides (NAD, NADH, and NADP) did not appreciably affect NAPE synthase activity. Initial velocity measurements of NAPE synthase activity at increasing concentrations of palmitic acid showed non-Michaelis-Menten, biphasic kinetics. A high-affinity site (S0.5 = 7.2 [mu]M, Vmax = 18.8 nmol h-1 mg-1 of protein) and a low-affinity site (S0.5 = 32.0 [mu]M, Vmax = 44.9 nmol h-1 mg-1 of protein) were identified. Both sites exhibited positive cooperativity. Adding myristic, stearic, or oleic acids at equimolar amounts reduced the incorporation of [14C]palmitic acid into NAPE at low concentrations (10 [mu]M, high-affinity site) but not at high concentrations (50 [mu]M, low-affinity site), indicating that the two putative sites can be distinguished by their fatty acid preferences. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

McArthur, DAJ.; Knowles, N. R.

doi: 10.1104/pp.102.3.771pmid: 12231865

Abstract Growth, development, and mineral physiology of potato (Solanum tuberosum L.) plants in response to infection by three species of vesicular-arbuscular mycorrhizal (VAM) fungi and different levels of P nutrition were characterized. P deficiency in no-P and low-P (0.5 mM) nonmycorrhizal plants developed between 28 and 84 d after planting. By 84 d after planting, P deficiency decreased plant relative growth rate such that no-P and low-P plants had, respectively, 65 and 45% less dry mass and 76 and 55% less total P than plants grown with high P (2.5 mM). A severe reduction in leaf area was also evident, because P deficiency induced a restriction of lateral bud growth and leaf expansion and, also, decreased the relative plant allocation of dry matter to leaf growth. Root growth was less influenced by P deficiency than either leaf or stem growth. Moreover, P-deficient plants accumulated a higher proportion of total available P than high-P plants, indicating that P stress had enhanced root efficiency of P acquisition. Plant P deficiency did not alter the shoot concentration of N, K, Mg, or Fe; however, the total accumulation of these mineral nutrients in shoots of P-stressed plants was substantially less than that of high-P plants. P uptake by roots was enhanced by each of the VAM symbionts by 56 d after planting and at all levels of abiotic P supply. Species differed in their ability to colonize roots and similarly to produce a plant growth response. In this regard, Glomus intraradices (Schenck and Smith) enhanced plant growth the most, whereas Glomus dimorphicum (Boyetchko and Tewari) was least effective, and Glomus mosseae ([Nicol. and Gerd.] Gerd. and Trappe) produced an intermediate growth response. The partial alleviation of P deficiency in no-P and low-P plants by VAM fungi stimulated uptake of N, K, Mg, Fe, and Zn. VAM fungi enhanced shoot concentrations of P, N, and Mg by 28 d after planting and, through a general improvement of overall plant mineral nutrition, promoted plant growth and development. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Wilson, I. D.; Zhu, Y.; Burmeister, D. M.; Dilley, D. R.

doi: 10.1104/pp.102.3.783pmid: 8278533

Abstract The apple ripening-related cDNA insert of clone pAP4 (G.S. Ross, M.L. Kinghton, M. Lay-Yee [1992] Plant Mol Biol 19: 231–)238) has previously been shown to have considerable nucleic acid and predicted amino acid sequence similarity to the insert of a tomato ripening-related cDNA clone (pTOM13) that is known to encode the enzyme 1-aminocyclopropane-1-carboxylate (ACC) oxidase (A.J. Hamilton, G.W. Lycett, D. Grierson [1990] Nature 346: 284–287; A.J. Hamilton, M. Bouzayen, D. Grierson [1991] Proc Natl Acad Sci USA 88: 7434–7437). The cDNA insert from the clone pAP4 was fused between the galactose-inducible promoter and the terminator of the yeast expression vector pYES2. Transformation of Saccharomyces cerevisiae strain F808- with this DNA construct and incubation of the yeast in the presence of D[+]-galactose allowed these cells to convert ACC to ethylene. The transformed yeast converted 1-amino-2-ethylcyclopropane-1-carboxylate isomers to 1-butene with the same 1R,2S-stereoselectivity as achieved by the native ACC oxidase from apples. Both ascorbate and Fe2+ ions stimulated the rate of the production of ethylene from ACC by the transformed yeast, whereas Cu2+ and Co2+ were strongly inhibitory; these are features of ACC oxidase. Northern analysis of the total RNA from nontransformed and transformed yeast showed that the ability to convert the ACC to ethylene was correlated with the synthesis and accumulation of a novel 1.2-kb mRNA that hybridized to the cDNA clone pAP4. We conclude that the cDNA sequence of the clone pAP4 encodes ACC oxidase. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

Lawrence, S. D.; Cline, K.; Moore, G. A.

doi: 10.1104/pp.102.3.789pmid: 12231866

Abstract The chloroplast to chromoplast transition during tomato (Lycopersicon esculentum Mill.) fruit ripening is characterized by a dramatic change in plastid structure and function. We have asked whether this process is mediated by an increase in the steady-state level of RNA for plastid targeted proteins. Assays for import of radiolabeled translation products into isolated pea (Pisum sativum L.) chloroplasts were used to monitor levels of chromoplast-targeted proteins at four stages of tomato fruit development. We have found striking increases during development in levels of translatable RNA for two such proteins. Additionally, the import of in vitro translation products was examined for seven individual cDNA clones known to encode RNA that increase during fruit ripening. Three of these clones produced in vitro translation products that were imported into pea chloroplasts. This implies that there is synthesis and import of new proteins during the transition from chloroplast to chromoplast and that the plastid conversion is an active developmental program rather than a simple decline in synthesis of the photosynthetic apparatus. Furthermore, our results demonstrate the utility of this method for identification of structural genes involved in plastid morphogenesis. This content is only available as a PDF. Copyright © 1993 by American Society of Plant Biologists This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)