نتایج جستجو برای: psi bounded

تعداد نتایج: 73401  

Journal: :Plant physiology 2002
Claudio Varotto Paolo Pesaresi Peter Jahns Angela Lessnick Marco Tizzano Fabio Schiavon Francesco Salamini Dario Leister

Photosystem I (PSI) of higher plants contains 18 subunits. Using Arabidopsis En insertion lines, we have isolated knockout alleles of the genes psaG, psaH2, and psaK, which code for PSI-G, -H, and -K. In the mutants psak-1 and psag-1.4, complete loss of PSI-K and -G, respectively, was confirmed, whereas the residual H level in psah2-1.4 is due to a second gene encoding PSI-H, psaH1. Double muta...

2005
L. ANDREW STAEHELIN

We have used the nonionic detergent octyl-O-D-glucopyranoside in combination with sodium dodecyl sulfate to isolate two novel Photosystem I (PSI) complexes from spinach (Spinacea oleracea L.) thylakoid membranes. These complexes have been characterized as to their spectral properties, content of PSI reaction center chlorophyll P7-, and protein composition. PSI-B, purified from solubilized membr...

Journal: :Plant physiology 1984
M E Westgate J S Boyer

Recent evidence from leaves and stems indicates that gradients in water potential (psi(w)) necessary for water movement through growing tissues are larger than previously assumed. Because growth is sensitive to tissue psi(w) and the behavior of these gradients has not been investigated in transpiring plants, we examined the water status of all the growing and mature vegetative tissues of maize ...

Journal: :The Journal of biological chemistry 2015
Clotilde Le Quiniou Bart van Oort Bartlomiej Drop Ivo H M van Stokkum Roberta Croce

Photosystems (PS) I and II activities depend on their light-harvesting capacity and trapping efficiency, which vary in different environmental conditions. For optimal functioning, these activities need to be balanced. This is achieved by redistribution of excitation energy between the two photosystems via the association and disassociation of light-harvesting complexes (LHC) II, in a process kn...

Journal: :Physical review letters 2006
T E Coan Y S Gao F Liu M Artuso C Boulahouache S Blusk J Butt O Dorjkhaidav J Li N Menaa R Mountain R Nandakumar K Randrianarivony R Redjimi R Sia T Skwarnicki S Stone J C Wang K Zhang S E Csorna G Bonvicini D Cinabro M Dubrovin A Lincoln R A Briere G P Chen J Chen T Ferguson G Tatishvili H Vogel M E Watkins J L Rosner N E Adam J P Alexander K Berkelman D G Cassel V Crede J E Duboscq K M Ecklund R Ehrlich L Fields R S Galik L Gibbons B Gittelman R Gray S W Gray D L Hartill B K Heltsley D Hertz C D Jones J Kandaswamy D L Kreinick V E Kuznetsov H Mahlke-Krüger T O Meyer P U E Onyisi J R Patterson D Peterson E A Phillips J Pivarski D Riley A Ryd A J Sadoff H Schwarthoff X Shi M R Shepherd S Stroiney W M Sun D Urner T Wilksen K M Weaver M Weinberger S B Athar P Avery L Breva-Newell R Patel V Potlia H Stoeck J Yelton P Rubin C Cawlfield B I Eisenstein G D Gollin I Karliner D Kim N Lowrey P Naik C Sedlack M Selen E J White J Williams J Wiss D M Asner K W Edwards D Besson T K Pedlar D Cronin-Hennessy K Y Gao D T Gong J Hietala Y Kubota T Klein B W Lang S Z Li R Poling A W Scott A Smith S Dobbs Z Metreveli K K Seth A Tomaradze P Zweber J Ernst H Severini S A Dytman W Love S Mehrabyan J A Mueller V Savinov Z Li A Lopez H Mendez J Ramirez G S Huang D H Miller V Pavlunin B Sanghi I P J Shipsey G S Adams M Anderson J P Cummings I Danko J Napolitano Q He H Muramatsu C S Park E H Thorndike

From e(+)e(-) collision data acquired with the CLEO detector at the Cornell Electron Storage Ring, we observe the non-DD(_) decay Psi(3770))-->gammachi(c1) with a statistical significance of 6.6 standard deviations, using the two-photon cascades to J/Psi and J/Psi-->l(+)l(-). We determine sigma(e(=)e(-)-->Psi(3770))xBeta(Psi(3770)-->gammachi(c1))=(18.0 +/- 3.3 +/- 2.5) pb and branching fraction...

Journal: :AIMS mathematics 2021

In this paper, we study the Hyers-Ulam stability with respect to linear differential condition of fourth order. Specifically, treat ${\psi}$ as an interact arrangement condition, i.e., $ \begin{align*} {\psi}^{iv} ({\varkappa}) + {\xi}_1 {\psi}{'''} ({\varkappa})+ {\xi}_2 {\psi}{''} {\xi}_3 {\psi}' {\xi}_4 {\psi}({\varkappa}) = {\Psi}({\varkappa}) \end{align*} $ where ${\psi} \in c^...

Journal: :Plant physiology 1990
G E Welbaum K J Bradford

The initiation of radicle growth during seed germination may be driven by solute accumulation and increased turgor pressure, by cell wall relaxation, or by weakening of tissues surrounding the embryo. To investigate these possibilities, imbibition kinetics, water contents, and water (Psi) and solute (psi(s)) potentials of intact muskmelon (Cucumis melo L.) seeds, decoated seeds (testa removed, ...

Journal: :Genetics 2010
Alex K Lancaster J Patrick Bardill Heather L True Joanna Masel

Epigenetically inherited aggregates of the yeast prion [PSI+] cause genomewide readthrough translation that sometimes increases evolvability in certain harsh environments. The effects of natural selection on modifiers of [PSI+] appearance have been the subject of much debate. It seems likely that [PSI+] would be at least mildly deleterious in most environments, but this may be counteracted by i...

Journal: :Journal of virology 2007
Samuel J Rulli Catherine S Hibbert Jane Mirro Thoru Pederson Shyam Biswal Alan Rein

Assembly of retrovirus particles normally entails the selective encapsidation of viral genomic RNA. However, in the absence of packageable viral RNA, assembly is still efficient, and the released virus-like particles (termed "Psi-" particles) still contain roughly normal amounts of RNA. We have proposed that cellular mRNAs replace the genome in Psi- particles. We have now analyzed the mRNA cont...

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