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Characterization of PII and truncated PII transgenic, Arabidopsis thaliana.

Wong Lee. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2001. / Includes bibliographical references (leaves 152-169). / Abstracts in English and Chinese. / Thesis Committee --- p.i / Abstract --- p.ii / 摘要 --- p.iv / Acknowledgements --- p.v / Abbreviations --- p.vi / List of Figures --- p.vii / List of Tables --- p.ix / Table of Contents --- p.xi / Chapter 1 --- Literature Review --- p.1 / Chapter 1.1 --- GS-GOGAT cycle in plants and bacteria --- p.2 / Chapter 1.2 --- Roles of PII in regulation of glutamine synthetase in E. coli --- p.4 / Chapter 1.2.1 --- Regulation of GS in E. col --- p.4 / Chapter 1.2.2 --- Transcriptional regulation --- p.5 / Chapter 1.2.2.1 --- The glnALG operon / Chapter 1.2.2.2 --- Intracellular signal through PII and Utase-UR / Chapter 1.2.2.3 --- NRI/NRII as two-component system / Chapter 1.2.3 --- Post-translational regulation by adenylylation and deadenylylation --- p.11 / Chapter 1.2.3.1 --- Role of PII in adenylylation/deadenylylation / Chapter 1.2.4 --- Cumulative Feedback Inhibition --- p.15 / Chapter 1.3 --- PII in other bacteria --- p.15 / Chapter 1.4 --- PII in other higher organisms --- p.20 / Chapter 1.5 --- "PII protein is conserved in enteric bacteria, cyanobacteria, archaea, algae and higher plants" --- p.23 / Chapter 1.6 --- Nitrogen assimilation in higher plants --- p.25 / Chapter 1.6.1 --- Nitrogen uptake --- p.25 / Chapter 1.6.2 --- Primary nitrogen assimilation --- p.28 / Chapter 1.6.3 --- Nitrogen transport and interconversions --- p.28 / Chapter 1.6.4 --- Nitrogen flow --- p.29 / Chapter 1.6.5 --- Molecular regulation of nitrogen assimilation and possible roles of PII in plants --- p.30 / Chapter 1.7 --- Hypothesis of this study --- p.33 / Chapter 2. --- Materials and Methods --- p.35 / Chapter 2.1 --- Materials --- p.35 / Chapter 2.1.1 --- Plant materials --- p.35 / Chapter 2.1.2 --- Equipment and facilities used --- p.35 / Chapter 2.1.3 --- Growth media --- p.37 / Chapter 2.1.4 --- Buffers and solutions used in RNA extraction --- p.38 / Chapter 2.1.5 --- Buffers and solutions used in Northern blot analysis --- p.41 / Chapter 2.1.6 --- Molecular reagents and synthetic oligonucleotides used in the preparation of DIG-labeled probes --- p.45 / Chapter 2.1.7 --- Chemicals used in BioRad Protein Assay --- p.48 / Chapter 2.1.8 --- Chemicals and apparatus used in chlorophylls extraction and quantitation --- p.49 / Chapter 2.1.9 --- Buffers and solutions used in the glutamine synthetase enzyme extraction and assay --- p.49 / Chapter 2.2 --- Methods --- p.50 / Chapter 2.2.1 --- Plant growth --- p.50 / Chapter 2.2.2 --- RNA extraction --- p.52 / Chapter 2.2.3 --- Northern blot analysis --- p.54 / Chapter 2.2.4 --- Chlorophyll extraction and quantitation --- p.61 / Chapter 2.2.5 --- Root length measurement --- p.61 / Chapter 2.2.6 --- Total glutamine synthetase enzyme assay --- p.61 / Chapter 2.2.7 --- Measurement of total nitrogen in seeds --- p.64 / Chapter 2.2.8 --- Recording growth and development --- p.64 / Chapter 3. --- Results --- p.65 / Chapter 3.1 --- Overexpression ofPII and truncated PII mRNA in transgenic plants --- p.65 / Chapter 3.2 --- General growth characteristics of PII transgenic plants when grown on soil --- p.70 / Chapter 3.3 --- Physiological changes in the PII and truncated PII transgenic lines --- p.72 / Chapter 3.3.1 --- Fresh weight of the young seedlings --- p.73 / Chapter 3.3.2 --- Chlorophyll contents of shoots --- p.75 / Chapter 3.3.3 --- Root lengths --- p.88 / Chapter 3.3.4 --- Carbon and nitrogen status of seeds --- p.94 / Chapter 3.4 --- Expression of nitrogen assimilatory genes in PII and truncated PII transgenic lines --- p.96 / Chapter 3.4.1 --- Nitrate reductases --- p.96 / Chapter 3.4.2 --- Glutamine synthetases --- p.99 / Chapter 3.4.3 --- Asparagine synthetases --- p.107 / Chapter 3.5 --- Total glutamine synthetase enzyme activity --- p.117 / Chapter 4. --- Discussion --- p.126 / Chapter 4.1 --- Overexpressing PII and truncated PII in the transgenic plants --- p.126 / Chapter 4.2 --- The overall growth and development --- p.135 / Chapter 4.3 --- Chlorophyll --- p.135 / Chapter 4.4 --- Root length --- p.137 / Chapter 4.5 --- Expression of nitrogen assimilatory genes --- p.138 / Chapter 4.5.1 --- Genes encoding nitrate reductase --- p.138 / Chapter 4.5.2 --- Genes encoding glutamine synthetase --- p.140 / Chapter 4.5.3 --- Genes encoding asparagine synthetase --- p.141 / Chapter 4.6 --- Overall GS enzyme levels in the rosette leaves --- p.144 / Chapter 4.7 --- N/C ratio of the seed storage --- p.146 / Chapter 4.8 --- Proposed model for the roles of PII --- p.147 / Chapter 4.9 --- Conclusions --- p.149 / Chapter 4.10 --- Further studies --- p.150 / References --- p.152

Identiferoai:union.ndltd.org:cuhk.edu.hk/oai:cuhk-dr:cuhk_323432
Date January 2001
ContributorsWong, Lee., Chinese University of Hong Kong Graduate School. Division of Biology.
Source SetsThe Chinese University of Hong Kong
LanguageEnglish, Chinese
Detected LanguageEnglish
TypeText, bibliography
Formatprint, xiv, 169 leaves : ill. ; 30 cm.
RightsUse of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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