Ribosomes which conduct protein synthesis in all living organisms are comprised of two subunits. The large 60S ribosomal subunit catalyzes peptidyl transferase reactions and includes the polypeptide exit tunnel, while the small (40S) ribosomal subunit recruits incoming messenger RNAs (mRNAs) and performs proofreading. The plant 80S cytoplasmic ribosome is composed of 4 ribosomal RNAs (rRNAs: 25-28S, 5.8S and 5S in the large subunit and 18S in the small subunit) and 81 ribosomal proteins (r-proteins: 48 in the large subunit, 33 in the small subunit). RPS15a, a putative small subunit primary binder, is encoded by a six member gene family (RPS15aA-F), where RPS15aB and RPS15aE are evolutionarily distinct and thought to be incorporated into mitochondrial ribosomes. In vitro synthesized cytoplasmic 18S rRNA, 18S rRNA loop fragments, and RPS15a mRNA molecules were combined in electrophoretic shift assays (EMSAs) to determine the RNA binding characteristics of RPS15aA/-D/-E/-F. RPS15aA/F, -D and -E bind to cytoplasmic 18S rRNA in the absence of cellular components. However, RPS15aE r-protein tested that binds mitochondrial 18S rRNA. In addition, RPS15aA/F only binds one of three 18S rRNA loop fragments of helix 23 whereas RPS15aD/-E bind all three 18S rRNA helix 23 loop fragments. Additionally, RPS15aD and RPS15aE did not bind their respective mRNA transcripts, likely indicating that this form of negative feedback is not a post-transcriptional control mechanism for this r-protein gene family. Furthermore, the addition of RPS15a transcripts to the EMSAs did not affect the binding of RPS15aA/F, -D and -E to 18S rRNA helix 23 loop 4-6, indicating that rRNA binding is specific. Supershift EMSAs further confirmed the specificity of RPS15aA/F and RPS15aE binding to loop fragment (4-6) of 18S rRNA. Taken together, these data support a role for RPS15a in early ribosome small subunit assembly.

The brevipedicellus (bp) mutant, caused by a loss-of-function mutation in the KNAT1 homeobox gene, is known to affect the stem morphogenesis. BP and ERECTA (ER) genes are required to promote internode and pedicel development and delineate nodal boundaries to maintain the radial symmetry of stems and pedicels. My research aims to identify genes acting on the BP pathway by utilizing a forward genetics approach. The suppressor4 mutant, identified from the bp er mutant screen, exhibits moderate length and perpendicularly-oriented pedicels with partially formed distal pedicel bulges, absent in the bp mutant. The kinky mutant, identified from the bp mutant screen, develops severe bends at the floral nodes and enhanced achlorophyllous stripes. These results suggest the SUPPRESSOR4 gene contribution in inhibiting the development of distal pedicel bulge and influencing both pedicel angle and length whereas the KINKY gene might act with BP in regulating proper inflorescence development.

Bibliography: leaves 153-185. / [ix], 200, [29] leaves, [6] leaves of plates : ill. (chiefly col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Vesicular-arbuscular (VA) mycorrhiza formation is a complex process which is under the genetic control of both plant and fungus. This project aims to develop a model infection system in Hordeum vulgare L. (barley) suitable for molecular analysis; to identify host plant genes differentially expressed during the early stages of the infection process; and to screen a mutant barley population for phenotypes which form abnormal mycorrhizas. / Thesis (Ph.D.)--University of Adelaide, Dept. of Plant Science, 1995

Thesis (Ph. D.)--University of Adelaide, Dept. of Plant Science, 1996? / Includes bibliographical references (leaves 153-185).

Doctor of Philosophy / Department of Biology / Jyoti Shah / Localized inoculation of a plant with an avirulent pathogen results in the activation of systemic acquired resistance (SAR), a defense mechanism that confers enhanced resistance against a variety of pathogens. The activation of SAR requires the translocation of an unknown signal from the pathogen-inoculated organ to the other organs where defenses are primed to respond faster in response to a future attack by a pathogen. Previous studies with the Arabidopsis thaliana dir1 (defective in induced resistance1) and sfd1 (suppressor of fatty acid desaturase deficiency1) mutants implicated a role for plant lipids in the activation of SAR. DIR1 encodes a putative lipid transfer protein and SFD1 encodes a dihydroxyacetone phosphate (DHAP) reductase involved in plastid glycerolipid metabolism. To further evaluate the role of DHAP reductases and plastid lipids in SAR, the involvement of two additional putative DHAP reductase encoding genes (AtGPDHp and AtGPDHc) and the SFD2 gene, which like SFD1 is involved in plastid glycerolipid metabolism, in SAR was evaluated. Only SFD2 was found to be essential for SAR. Although the lipid profile of the sfd2 mutant was similar to that of the fad5 (fatty acid desaturase 5) mutant, sfd2 is not allelic with fad5 and does not influence FAD5 expression. The SFD2 gene was mapped to an 85 kilo basepairs (kb) region on the third chromosome of Arabidopsis. The lipid composition defect of the sfd2 mutant was partially complemented by two independent recombinant bacterial artificial chromosomes (BACs) that contained genomic DNA spanning the wild type SFD2 locus. The role of plastid synthesized glycerolipids in the activation of SAR was further evaluated by characterizing SAR in additional Arabidopsis mutants that were deficient in plastid lipid metabolism. The requirement of MGD1 (MONOGALACTOSYLDIACYLGLYCEROL SYNTHASE 1), DGD1 (DIGALACTOSYL-DIACYLGLYCEROL SYNTHASE 1) and FAD7 (FATTY ACID DESATURASE 7) genes in SAR, confirmed the essential role of plastid glycerolipids, presumably a galactolipid-dependent factor, in signaling associated with the SAR.

y-Aminonbutyric acid (GABA) is a ubiquitous non-protein amino acid found ill many plants and organisms. GABA accumulation in plants has previously been reported as result of stresses such as water deprivation, high salinity and temperature extremes. It is thought that GABA accumulates as a compatible solute in the cytoplasm where it becomes a major constituent of the free amino acid pool. GABA is synthesised from the decarboxylation of glutamate by glutamate decarboxylase (GDC). In some plants, GDC is activated by the lowering of the cytoplasmic pH and the presence of calmodulin and Ca²+ A calmodulin-induced activation of may be due to the physiological factors and environmental stimuli acting in concert leading to the synthesis and accumulation of GABA. The GABA content of Arabidopsis thaliana var. Columbia (L) Heynh leaves was found to increase by over 130% due to water deprivation. NaCl concentrations of up to 100 mM seemed to cause GABA accumulation due to a decrease in osmotic potential. Concentrations of NaCl above 100 mM probably caused GABA accumulation due to combined hyperosmosis and salt toxicity effects. The high levels of GABA in the leaves were maintained throughout a 24 h stress-application period, consistent with its role as compatible solute. The accumulation of GABA followed by its decline in the dark could be attributed to its rapid metabolism because of an active GABA shunt. This is in contrast to the absence of major variations in the amount of GABA in the light confirming its decreased role as a channel for the glutamate carbon and nitrogen under such conditions. A substantial increase in the GABA content was followed by a dramatic decrease in the last 12 h of incubation. This profile of GABA could support its proposed role as a temporary sink for nitrogen and carbon from glutamate during environmental stress. Glutamate decarboxylase appears to be encoded by a single gene in the genome of Arabidopsis. Sequence analysis reveals that the protein possesses what could be a carboxy-terminal, calmodulin- binding domain, which is consistent with other glutamate decarboxylases. The 30-amino acid peptide contains a TrpLysLys motif found in some calmodulin targets. The secondary structure predictions of this peptide suggest a potential to form an a- helix which is also consistent with proteins known calmodulin- binding domains. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 1997.

In Arabidopsis thaliana (L.) Heyhn, the size of the pool of free proline increases up to 27-fold in response to osmotic stress. The magnitude of this accumulation is dependent upon the rate of imposition of the stress. Numerous reports have suggested a role for proline accumulation as a general adaptation to environmental stress. However, controversy surrounds the beneficial effect of proline accumulation in plants under adverse environmental conditions. Stress-induced proline accumulation in plants occurs mainly by de novo synthesis from glutamate. The final and only committed step of proline biosynthesis in plants is catalysed by Δ¹-pyrroline-5-carboxylate reductase (P5CR). The sequence of an incomplete 999 bp cDNA encoding P5CR from A. thaliana was determined. This enabled a preliminary molecular study of the structure and function of both the gene and the corresponding enzyme. The 999 bp cDNA insert in the clone Y AP057 was sequenced on the sense and antisense strands following subcloning of four sub-fragments in appropriate orientations. Comparison with known plant P5CR sequences revealed that Y AP057 does not encode the first 23 N-terminal amino acids of P5CR from Arabidopsis. However, it does encode the remaining 253 amino acid residues of Arabidopsis P5CR The cDNA Y AP057 is complete on the 3' end as indicated by the presence of a poly(A) tail. The nucleotide sequence determined shows complete homology to the corresponding exons of the genomic copy of a bona fide gene encoding P5CR in A. thaliana (Verbruggen et al, 1993). The only difference observed between the sequence of Y AP057 and that of a cDNA sequenced by these workers is that polyadenylation was initiated seven nucleotides earlier in Y AP057 than in the sequence of the published cDNA. Genomic Southern analysis suggests the presence of only a single copy of the gene encoding P5CR in Arabidopsis. Restriction mapping and sequencing the ends of another incomplete Arabidopsis P5CR cDNA clone FAFJ25 (664 bp) indicated that the regions sequenced were completely homologous to the corresponding portions of Y AP057. Analysis of codon usage in the Arabidopsis gene encoding P5CR revealed it to closely resemble the consensus pattern of codon usage in A. thaliana. This suggests that the gene is moderately. expressed. Expression of the gene encoding P5CR in Arabidopsis is not likely to be subject to translational control. Although P5CR from A. thaliana has a fairly high composition of hydrophobic amino acid residues, it does not possess any stretches of hydrophobic amino acids of sufficient length to act as membrane-spanning domains or to anchor the enzyme in a membrane. Neither does it contain an N- terminal leader sequence capable of directing it to either the plastid or mitochondrion. The enzyme therefore appears to be cytosolic. The nucleic acid and deduced amino acid sequences of Arabidopsis P5CR were compared with those from·eleven other organisms for which P5CR sequences are currently available. Except among the three different plants examined, P5CR sequences displayed less identity at the amino acid level than at the nucleotide level. The deduced amino acid sequence of Arabidopsis P5CR exhibits high similarity to the corresponding genes and amino acid sequences of P5CR from soybean and pea. Lower but significant similarity was observed to the amino acid sequences of P5CRs from human, Saccharomyces cerevisiae and the bacteria Escherichia coli, Pseudomonas aeruginosa, Thermus thermophilus, Mycobacterium leprae; Treponema pallidum and Methanobrevibacter smithii. Similarity was also observed to the translational product of a gene from Bacillus subtilis with high homology to the E. coli proC gene. However, construction of a phenogram indicating the relatedness of the various P5CR enzymes suggests that sequence analysis of this enzyme is not a good indicator of evolutionary relatedness of organisms from different biological kingdoms. Multiple alignment of the twelve known P5CR sequences indicated homology between the sequences across their entire lengths. Homology was particularly high in the C-terminal portions of the P5CRs studied. It is speculated that this region may be of importance in binding of the substrate Δ¹-pyrroline-S-carboxylate (P5C). Another region displaying high sequence conservation was found in the central portion of all P5CRs. All P5CRs studied, with the exception of PSCR from T. pallidum contained an N-terminal domain capable of binding a nicotinamide dinucleotide cofactor. Comparison of this region with consensus sequences for NADH and NADPH binding sites in proteins suggests that NADPH is the preferred reductant used by P5CRs from plants and human. In contrast, the N-terrninal domains of P5CRs from S. cerevisiae, M smithii, T. thermophilus and M leprae display greater similarity to a consensus NADH-binding site. The definite preference of plant P5CRs for NADPH in comparison with NADH suggests that P5CR may be involved in regulating the redox potential within plant cells and that this step in proline biosynthesis from glutamate may be of importance in overall metabolic regulation. Three amino acid residues are universally conserved in all P5CRs studied. All are found within blocks of high sequence similarity. These residues are likely to be of importance in the structure or catalytic mechanism of P5CR. A number of other residues are common to several of the enzymes examined. These may also be of importance in subsequent manipulation of Arabidopsis P5CR at the molecular level. Prediction of the putative secondary structures of A. thaliana, soybean, pea, human and E. coli indicated a high degree of similarity between the enzymes. This was particularly evident in the region of the putative P5C-binding domain. Considerable similarity exists in hydrophobicity profiles of P5CRs from these five organisms. Proline levels in reproductive organs of unstressed Arahidopsis plants were considerably higher than those in vegetative tissues. This suggests differential expression of enzymes involved in proline metabolism in these organs. In situ hybridisation studies indicated an increase in levels of mRNA transcripts encoding P5CR in stem tissues in response to water deprivation stress. Regulation of levels of mRNA transcript encoding P5CR in Arabidopsis therefore appears to be an osmotically sensitive process. Furthermore, this accumulation of transcript occurred in a tissue-specific manner. In particular, an increase in levels of transcript encoding P5CR was observed in the cortical parenchyma, phloem, vascular cambium and pith parenchyma in the vicinity of the protoxylem. The significance of these findings in contributing to a better understanding of the role of proline in adaptation to environmental stress is discussed. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 1995.

This thesis examines the interaction of xyloglucan, the major hemicellulosic component of type I primary plant cell walls, with cellulose. Initial attempts to form xyloglucan-cellulose complexes by in vitro association methods are described, which gave low levels of interaction, with features not similar to those found in primary wall networks. The majority of the work focusses on the use of the bacterium Acetobacter aceti ssp. xylinum (ATCC 53524), which synthesise highly pure, crystalline cellulose as an extracellular polysaccharide. Addition of xyloglucan to a cellulose-synthesising bacterial culture results in the formation of cellulose-xyloglucan networks with ultrastructural and molecular features similar to those of the networks of higher plants. Applicatioon of the bacterial fermentation system is extended to incorporate the polysaccharides glucomannan, galactomannan, xylan, mixed-linkage glucan, pectin and carboxymethylcellulose, all of which impart unique architectural and molecular effects on the composistes formed. Preliminary data on the mechanical properties of composite structures under large and small deformation conditions are also described.

Thesis (M.S.)--University of North Carolina at Wilmington, 2005. / Includes bibliographical references (leaves: 128-132)

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