Joseph Ackerman

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Name: Ackerman, Joseph
Organization: Washington University in St. Louis , USA
Department: Departments of Chemistry, Internal Medicine
Title: Professor(PhD)
Co-reporter:Xia Ge, D. André d’Avignon, Joseph J. H. Ackerman, Alberto Collavo, Maurizio Sattin, Elizabeth L. Ostrander, Erin L. Hall, R. Douglas Sammons, and Christopher Preston
Journal of Agricultural and Food Chemistry 2012 Volume 60(Issue 5) pp:1243-1250
Publication Date(Web):January 4, 2012
DOI:10.1021/jf203472s
Lolium spp., ryegrass, variants from Australia, Brazil, Chile, and Italy showing differing levels of glyphosate resistance were examined by 31P NMR. Extents of glyphosate (i) resistance (LD50), (ii) inhibition of 5-enopyruvyl-shikimate-3-phosphate synthase (EPSPS) activity (IC50), and (iii) translocation were quantified for glyphosate-resistant (GR) and glyphosate-sensitive (GS) Lolium multiflorum Lam. variants from Chile and Brazil. For comparison, LD50 and IC50 data for Lolium rigidum Gaudin variants from Italy were also analyzed. All variants showed similar cellular uptake of glyphosate by 31P NMR. All GR variants showed glyphosate sequestration within the cell vacuole, whereas there was minimal or no vacuole sequestration in the GS variants. The extent of vacuole sequestration correlated qualitatively with the level of resistance. Previous 31P NMR studies of horseweed (Conyza canadensis (L.) Cronquist) revealed that glyphosate sequestration imparted glyphosate resistance. Data presented herein suggest that glyphosate vacuolar sequestration is strongly contributing, if not the major contributing, resistance mechanism in ryegrass as well.
Co-reporter:Andrew M. Prantner;G. Larry Bretthorst;Jeffrey J. Neil;Joel R. Garbow;Joseph J.H. Ackerman
Magnetic Resonance in Medicine 2008 Volume 60( Issue 3) pp:555-563
Publication Date(Web):
DOI:10.1002/mrm.21671

Abstract

Longitudinal relaxation of brain water 1H magnetization in mammalian brain in vivo is typically analyzed on a per-voxel basis using a monoexponential model, thereby assigning a single relaxation time constant to all 1H magnetization within a given voxel. This approach was tested by obtaining inversion recovery (IR) data from gray matter of rats at 64 exponentially spaced recovery times. Using Bayesian probability for model selection, brain water data were best represented by a biexponential function characterized by fast and slow relaxation components. At 4.7T, the amplitude fraction of the rapidly relaxing component is 3.4% ± 0.7% with a rate constant of 44 ± 12 s−1 (mean ± SD; 174 voxels from four rats). The rate constant of the slow relaxing component is 0.66 ± 0.04 s−1. At 11.7T, the corresponding values are 6.9% ± 0.9%, 19 ± 5 s−1, and 0.48 ± 0.02 s−1 (151 voxels from four rats). Several putative mechanisms for biexponential relaxation behavior were evaluated, and magnetization transfer (MT) between bulk water protons and nonaqueous protons was determined to be the source of biexponential longitudinal relaxation. MR methods requiring accurate quantification of longitudinal relaxation may need to take this effect explicitly into account. Magn Reson Med 60:555–563, 2008. © 2008 Wiley-Liss, Inc.

Glycogen synthase kinase 3, GSK3β
3-((3-Chloro-4-hydroxyphenyl)amino)-4-(2-nitrophenyl)-1H-pyrrole-2,5-dione
Methyl-D-erythritol Phosphate
1,3,5,2,4-Trioxadiphosphocane-6-methanol, 2,4,7-trihydroxy-6-methyl-, 2,4-dioxide, (6S,7R)-
CARBOXYMETHYL-COENZYME A
ACETONYL-COENZYME A
NOCODAZOLE
2-Deoxy-2-fluoro-D-glucose
D-ribose 5-(dihydrogen phosphate)
HYDROGEN CARBONATE