Arabinogalactan proteins (AGPs) are highly glycosylated cell wall proteins specific to plants. AGPs have been implicated in almost all aspects of plant development and defense responses, nevertheless, most of such studies are correlative. To define the specific functions of individual AGPs, direct evidence from analyses of genetic knockout mutants of individual AGPs is required. Up to now, only a few AGPs have been demonstrated to have defined functions by mutant analyses. This dissertation identified a non-classical AGP (AGP31), described its expression and characterized the null mutant of AGP31 in Arabidopsis. In agp31 mutant, microarray analyses revealed that the expressions of genes encoding a subset of seed storage proteins (SSP): CRU3, CRA1 and OLEOSIN2 were induced. Further analysis showed that induction by agp31 knockout was specific to these three SSP genes, indicating a novel pathway to regulate the SSP gene expression. Comprehensive characterizations of AGP31 were carried out. Yariv reagent staining and monosaccharide analysis of purified AGP31 showed that AGP31 was a bona fide galactose-rich AGP. The cell wall localization of AGP31 was confirmed by expression of an AGP31::eGFP fusion protein. AGP31 promoter-GUS reporter gene analysis showed that AGP31 was expressed in the vascular bundle throughout the plant, except in the flower. In the flower, it was expressed throughout the pistil except in the stigma. Detailed analysis showed that GUS staining occurred in all cell types in the vascular bundle of roots, while GUS staining was restricted to phloem cells in the inflorescence stem. AGP31 mRNA was down-regulated by several stress treatments, including wounding, methyl jasmonic acid (MeJA) and abscisic acid (ABA). In response to MeJA treatment of whole seedlings, AGP31 mRNA level decreased to about 30% of its original level within 8 hr and almost returned to its original level after 24 hr. Nuclei run-on assay showed that the down-regulation of AGP31 mRNA upon MeJA treatment was due to reduced transcription. The strong preferential expression in vascular tissues and negative regulations by MeJA and ABA suggest that AGP31 may be involved in vascular tissue function both during development and the defense response.

No description available.

Thesis (Ph. D.)--University of Texas at Austin, 2007. / Vita. Includes bibliographical references.

Thesis (Ph. D.)--Ohio State University, 2003. / Title from first page of PDF file. Document formatted into pages; contains xiii, 395 p.; also includes graphics Includes bibliographical references (p. 383-395). Available online via OhioLINK's ETD Center

Thesis (Ph. D.)--Ohio University, March, 2004. / Includes bibliographical references (leaves 202-227).

Thesis (Ph. D.)--University of Missouri-Columbia, 2008. / The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed on August 4, 2009) Vita. Includes bibliographical references.

Lipoarabinomannan (LAM) and the mycolyl-arabinogalactan (mAG) complex are two major entities found in the cell wall of Mycobacterium tuberculosis, the bacterium that causes tuberculosis in humans. Given their important roles in the viability and virulence of the pathogen, enzymes involved in these pathways represent a rich source of potential therapeutic drug targets. As fundamental understanding of substrateenzyme interactions is often essential in the drug discovery process, the purpose of this study was to investigate the substrate specificities of an -(16)-mannosyltransferase (ManT) and a -(15,6)-galactofuranosyltransferase (GlfT2), two key enzymes involved in the biosynthesis of LAM and mAG, respectively. Although the ManT activity had been detected using an established radioactive assay, its substrate specificity remained poorly defined. The current study focused on the design, synthesis and evaluation of acceptor substrate analogs of ManT. Among those analogs prepared were those containing methoxy-, hydrogen-, and amino-substituted carbohydrate residues as well as epimeric derivatives. A homologous series of oxygen- and sulfur-linked mannosides were also prepared. Evaluation of these analogs revealed the steric requirements and hydrogen bonding interactions of the enzyme, and the effect of acceptor length on mannosyltransferase activity. Also, these results provided additional insight into the role of ManTs and allowed the current proposed pathway of LAM to be further revised. Another objective of the current study was to understand how GlfT2 catalyzes the alternating -(15) and -(16)-galactofuranosyl transfers in a single active site. A panel of mono- and dideoxy trisaccharide derivatives was synthesized, in which hydroxyl groups at either or both C-5 and C-6 positions on the sugar residues at the reducing ends were selectively removed. Biological evaluation of these analogs using a spectrophotometric assay, and structural analysis of some of the enzymatic products, showed that the removal of the hydroxyl group(s) in the acceptors appeared to have no dramatic effect on either GlfT2 activity or the regioselectivity of its galactosylation. These results suggest that groups other than the C-5 and C-6 hydroxyl groups of the acceptors are more critical for the enzyme catalysis. The identification of these key elements would be the further objective of this project. The results from these fundamental studies provide important information about how these enzymes interact with their substrates at the molecular level. More importantly, this work will serve as the basis for the further design of potential inhibitors, which are potential lead compounds for novel therapeutic agents that are active against tuberculosis.

No description available.

Thesis (Ph.D.)--Ohio University, March, 2007. / Title from PDF t.p. Includes bibliographical references.

Pinus radiata D. Don is an economically important plantation species to New Zealand that is susceptible to the wood quality flaw 'intra-ring checking'. Intra-ring checking is a term used to describe radial fractures that can occur in the earlywood portion of a growth ring, altering the appearance and resilience of the wood, thereby decreasing its economic value. This thesis presents a study that was part of a broad, ongoing collaborative investigation directed at understanding wood quality issues, with the long term goal of enhancement of future radiata pine crops. These investigations are funded by the Wood Quality Initiative Ltd., and involve basic science, field trials and engineering studies related to intra-ring checking. Specifically, the present study was designed to establish the effects of the mineral nutrients boron, calcium and magnesium on wood formation, to determine whether they are associated with intra-ring checking. This research was carried out in three stages. Firstly, the ultra-structural and biochemical properties of wood with intra-ring checking were examined to determine if specific features of the cell wall were associated with the incidence of intra-ring checks. Electron microscopy techniques revealed that the CML/S1 region of the cell wall often showed a decrease in CML lignin staining and S1 striations in wood with intra-ring checks. However, Klason and acetyl bromide assays did not show a change in lignin content. In order to understand how changes in the CML/S1 region of the cell wall may occur, methods were required that would allow for the observation of wood formation in a controlled environment. In the second stage of this study, an organ culture technique was successfully developed to allow for the growth of radiata pine cambial tissue, sandwiched between phloem and xylem, on a defined nutrient medium. This nutrient medium was manipulated, using ion-binding resins, to control the amount of boron, calcium and magnesium available to the growing tissues, to determine if variations in wood formation could be induced. In the final stage of this research, an extensive comparative examination of different techniques that could be used for the observation and measurement of selected wood properties was undertaken, in order to determine the efficacy of the organ cultures to study wood formation in an altered nutrient environment. Wood properties were examined for various stages of xylogenesis, beginning with cell division and expansion, followed by cell wall deposition, and lastly with the onset of lignification in order to define the success of the culture technique. Electron microscopy investigations suggested that in the presence of very little boron the CML/S1 wall showed darker striation deposits, while an increase in calcium availability, resulted in a more defined CML/S1/S2 wall region compared to the controls. Further examination of the cell walls suggested that pectin esterification and possibly lignification could also be increased by limited boron availability. However, in many of the observed and measured parameters of wood properties, a great deal of complex 'between-tree' and 'within-culture' variation was observed. The results show that elucidation of the association between nutrient availability and the incidence of intra-ring checking can not be established from this organ culture study. In a concurrent study, the preliminary investigation of arabinogalactan-proteins (AGPs) in radiata pine was undertaken. Radiata pine AGPs were positioned in the compound middle lamella of xylem cells, suggesting potential roles in cell-cell adhesion or cell-cell signalling. For the first time, radiata pine AGPs were isolated and characterized in terms of their protein and carbohydrate composition, both of which yielded features typical of AGPs in other plant species. Unique to radiata pine AGPs was the presence of a large proportion of 5-linked arabinose. While the precise function(s) of AGPs are unknown, the results obtained in this research have established a basis for further investigation into the potential for their involvement in wood formation. Overall, new tools have been established to facilitate future research on radiata pine, a commercially important species, and novel results have been obtained concerning the mechanisms of wood formation therein.