Academic literature on the topic 'Plant cell wall biochemistry'

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Journal articles on the topic "Plant cell wall biochemistry"

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Facchini, Peter J., Jillian Hagel, and Katherine G. Zulak. "Hydroxycinnamic acid amide metabolism: physiology and biochemistry." Canadian Journal of Botany 80, no. 6 (June 1, 2002): 577–89. http://dx.doi.org/10.1139/b02-065.

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Hydroxycinnamic acid amides (HCAAs) are a widely distributed group of plant secondary metabolites purported to function in several growth and developmental processes including floral induction, flower formation, sexual differentiation, tuberization, cell division, and cytomorphogenesis. Although most of these putative physiological roles for HCAAs remain controversial, the biosynthesis of amides and their subsequent polymerization in the plant cell wall are generally accepted as integral components of plant defense responses to pathogen challenge and wounding. Tyramine-derived HCAAs are commonly associated with the cell wall of tissues near pathogen-infected or wound healing regions. Moreover, feruloyltyramine and feruloyloctapamine are covalent cell wall constituents of both natural and wound periderms of potato (Solanum tuberosum) tubers, and are putative components of the aromatic domain of suberin. The deposition of HCAAs is thought to create a barrier against pathogens by reducing cell wall digestibility. HCAAs are formed by the condensation of hydroxycinnamoyl-CoA thioesters with phenylethylamines such as tyramine, or polyamines such as putrescine. The ultimate step in tyramine-derived HCAA biosynthesis is catalyzed by hydro xycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase (THT; E.C. 2.3.1.110). The enzyme has been isolated and purified from a variety of plants, and the corresponding cDNAs cloned from potato, tobacco (Nicotiana tabacum), and pepper (Capsicum annuum). THT exhibits homology with mammalian spermidine-spermine acetyl transferases and putative N-acetyltransferases from microorganisms. In this review, recent advances in our understanding of the physiology and biochemistry of HCAA biosynthesis in plants are discussed.Key words: hydroxycinnamic acid amides, hydroxycinnamoyl-CoA thioesters, metabolic engineering, phenylethylamines, plant cell wall, polyamines, secondary metabolism, tyramine.
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Varner, Joseph E., and Liang-Shiou Lin. "Plant cell wall architecture." Cell 56, no. 2 (January 1989): 231–39. http://dx.doi.org/10.1016/0092-8674(89)90896-9.

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Wojtaszek, P. "Organismal view of a plant and a plant cell." Acta Biochimica Polonica 48, no. 2 (June 30, 2001): 443–51. http://dx.doi.org/10.18388/abp.2001_3928.

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Cell walls are at the basis of a structural, four-dimensional framework of plant form and growth time. Recent rapid progress of cell wall research has led to the situation where the old, long-lasting juxtaposition: "living" protoplast--"dead" cell wall, had to be dropped. Various attempts of re-interpretation cast, however, some doubts over the very nature of plant cell and the status of the walls within such a cell. Following a comparison of exocellular matrices of plants and animals, their position in relation to cells and organisms is analysed. A multitude of perspectives of the biological organisation of living beings is presented with particular attention paid to the cellular and organismal theories. Basic tenets and resulting corollaries of both theories are compared, and evolutionary and developmental implications are considered. Based on these data, "The Plant Body"--an organismal concept of plants and plant cells is described.
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Bonetta, D. T., M. Facette, T. K. Raab, and C. R. Somerville. "Genetic dissection of plant cell-wall biosynthesis." Biochemical Society Transactions 30, no. 2 (April 1, 2002): 298–301. http://dx.doi.org/10.1042/bst0300298.

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The plant cell wall is a complex structure consisting of a variety of polymers including cellulose, xyloglucan, xylan and polygalacturonan. Biochemical and genetic analysis has made it possible to clone genes encoding cellulose synthases (CesA). A comparison of the predicted protein sequences in the Arabidopsis genome indicates that 30 divergent genes with similarity to CesAs exist. It is possible that these cellulose synthase-like (Csl) proteins do not contribute to cellulose synthesis, but rather to the synthesis of other wall polymers. A major challenge is, therefore, to assign biological function to these genes. In an effort to address this issue we have systematically identified T-DNA or transposon insertions in 17 Arabidopsis Csls. Phenotypic characterization of ‘knock-out’ mutants includes the determination of spectroscopic profile differences in mutant cell walls from wild-type plants by Fourier-transform IR microscopy. A more precise characterization includes cell wall fractionation followed by neutral sugar composition analysis by anionic exchange chromatography.
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Smith, C. J. "Biochemistry of plant cell walls." Endeavour 10, no. 1 (January 1986): 55. http://dx.doi.org/10.1016/0160-9327(86)90078-5.

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Gilbert, Harry J. "The Biochemistry and Structural Biology of Plant Cell Wall Deconstruction." Plant Physiology 153, no. 2 (April 20, 2010): 444–55. http://dx.doi.org/10.1104/pp.110.156646.

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Morris, V. J., A. P. Gunning, A. R. Kirby, A. Round, K. Waldron, and A. Ng. "Atomic force microscopy of plant cell walls, plant cell wall polysaccharides and gels." International Journal of Biological Macromolecules 21, no. 1-2 (August 1997): 61–66. http://dx.doi.org/10.1016/s0141-8130(97)00042-1.

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Gibeaut, David M., and Nicholas G. Carpita. "Biosynthesis of plant cell wall polysaccharides." FASEB Journal 8, no. 12 (September 1994): 904–15. http://dx.doi.org/10.1096/fasebj.8.12.8088456.

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Bruce, David M. "Mathematical modelling of the cellular mechanics of plants." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 358, no. 1437 (July 30, 2003): 1437–44. http://dx.doi.org/10.1098/rstb.2003.1337.

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The complex mechanical behaviour of plant tissues reflects the complexity of their structure and material properties. Modelling has been widely used in studies of how cell walls, single cells and tissue respond to loading, both externally applied loading and loads on the cell wall resulting from changes in the pressure within fluid–filled cells. This paper reviews what approaches have been taken to modelling and simulation of cell wall, cell and tissue mechanics, and to what extent models have been successful in predicting mechanical behaviour. Advances in understanding of cell wall ultrastructure and the control of cell growth present opportunities for modelling to clarify how growth–related mechanical properties arise from wall polymeric structure and biochemistry.
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Fry, S. C. "BIOCHEMISTRY OF PLANT CELL WALLS (Book)." Plant, Cell and Environment 9, no. 1 (January 1986): 85. http://dx.doi.org/10.1111/1365-3040.ep11614355.

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Dissertations / Theses on the topic "Plant cell wall biochemistry"

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Kirby, James. "Multiplicity and organisation of plant cell wall degrading enzymes in Ruminococcus flavefaciens 17." Thesis, University of Aberdeen, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362230.

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The Gram-positive, strictly anaerobic bacterium, R. flavefaciens, plays an important role in the degradation of plant cell wall polysaccharides in the rumen. There is a paucity of information available, however, regarding the multiplicity and organisation of R. flavefaciens cellulolytic and xylanolytic enzyme systems. A technique involving PCR amplification of DNA with primers designed from conserved sequences, followed by hybridisation of the PCR products to chromosomal DNA, has led to an estimate of xylanase gene multiplicity in R. flavefaciens. The xylanase-specific primers were also useful in the isolation and sequencing of a partial xylanase gene, xynC. Although R. flavefaciens 17 appears to produce a cellulose-binding enzyme-complex, none of the individual enzymes examined was found to bind cellulose in isolation. However, a 210 kDa protein which is present in the complex was shown to bind cellulose after isolation from a renatured SDS-gel. In order to look for genetic evidence for a cellulose-binding mechanism, sequencing of the R. flavefaciens 17 endoglucanase gene, endA, was completed from PCR products. The carboxy-terminus of the predicted endA product consists of a domain which is similar to dockerins found in Clostridium thermocellum polysaccharidases. Homologous domains are also found in the R. flavefaciens xylanases, XynB and XynD. As the C. thermocellum dockerin domains mediate binding to the 210 kDa scaffolding protein in the cellulosome complex, it is likely that the R. flavefaciens domains play a similar role in assembly of a cellulosome-like complex (Lamed and Bayer, 1994). A gene which maps approximately 1.5 kb downstream from endA on the R. flavefaciens 17 chromosome was sequenced and found to be homologous to nifS genes from nitrogen-fixing bacteria (Zheng et al, 1993). The R. flavefaciens NifS product catalyses the production of sulphur from cysteine, and is suspected to partake in the assembly of iron-sulphur clusters. The precise role of NifS is not yet known, but may be related to the degradation of crystalline cellulose.
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Bonham, Victoria Anne. "Secondary cell wall specific proteins in plants." Thesis, Royal Holloway, University of London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312839.

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Good, J. C. "The study of enzymes and primers involved in the initiation of chains of glucans." Thesis, University of Oxford, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375257.

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Ries, Laure Nicolas Annick. "Regulation of genes encoding enzymes involved in plant cell wall deconstruction in Trichoderma reesei." Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/13045/.

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This study describes the regulation of genes encoding plant cell wall-degrading enzymes in the presence of different carbon sources from the biotechnologically important fungus Trichoderma reesei. It was shown that different carbon sources influence fungal growth rate, biomass production and subsequent enzyme secretion. Several genes were identified and suggested to play a role in the development of conidia and in maintaining polarised growth. RNA-sequencing studies showed an increase in transcript levels of genes encoding enzymes involved in plant cell wall degradation (CAZy) as well as of genes encoding lipases, expansins, hydrophobins, G-protein coupled receptors and transporters when mycelia were cultivated in the presence of a lignocellulosic substrate (wheat straw). The encoded non-CAZy proteins were proposed to have accessory roles in carbohydrate deconstruction. A model for solid substrate recognition in T. reesei was described, based on the comparison with the one proposed for Aspergillus niger. Post-transcriptional regulation mediated by regulatory RNAs was identified for nearly 2% of all T. reesei genes, including genes encoding cell wall-degrading enzymes. Transcriptional regulation studies confirmed that transcription patterns of genes encoding enzymes involved in polysaccharide degradation differed between different carbon sources and that they are fine-tuned and dependent on factors such as culture conditions, consumption rate, assimilation of glucose and the presence of several transcription factors. The analysis of the structure of chromatin in the promoter and coding regions of one of these genes, cbh1, revealed different nucleosome positioning patterns under repressing (glucose) and inducing (sophorose, cellulose) conditions. CRE1, the carbon catabolite repressor in T. reesei was shown to be involved in the repression of many CAZy and non-CAZy encoding genes. Furthermore, CRE1 was also shown to be important for nucleosome positioning within the cbh1 coding region under repressing conditions and proposed to do so by interaction with (a) yet unidentified protein(s).
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Tao, Titus. "Functional characterization of ZmGRP5, a glycine-rich protein specifically expressed in the cell wall of maize silk tissue." Thesis, University of Ottawa (Canada), 2004. http://hdl.handle.net/10393/26780.

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Silk tissue is a specialized reproductive tissue of the maize plant, equivalent to the stigma and style portion of the female inflorescence. The moist and nutrient rich properties of maize silk tissue that facilitate pollen reception and the support of pollen tube growth also make maize silk a preferred site of infection by fungal pathogens such as Fusarium graminearum. The cDNA clone zmgrp5 was isolated in a previous study to identify silk tissue-specific genes. ZmGRP5, the encoded protein, was predicted to be a cell wall glycine-rich protein (GRP) and was experimentally characterized in this study. Using polyclonal antiserum, immunoblot analysis confirmed the silk tissue specificity of the protein. Additionally, subcellular fractionation studies confirmed ZmGRP5 localization in the cell wall fraction, and not in any other subcellular fractions. Interaction of ZmGRP5 with the cell wall matrix was observed to be disrupted by the addition of the reducing agent beta-ME. The reversible nature of disulfide bond formation and disruption under different redox conditions suggest that ZmGRP5 could potentially be important in the regulation of cell wall structural properties such as elasticity and rigidity in accordance with environmental and developmental changes. The variable immobilization of ZmGRP5 to the cell wall matrix could also serve as a potential mechanism of activation or inactivation of any non-structural functions. The identification of potential post-translational modifications such as phosphorylation and glycosylation, which are rarely observed in other cell wall GRPs, suggest that the functional significance of these modifications in ZmGRP5 is worthy of further study.
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Messenger, David James. "Impact of UV light on the plant cell wall, methane emissions and ROS production." Thesis, University of Edinburgh, 2009. http://hdl.handle.net/1842/4347.

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This study presents the first attempt to combine the fields of ultraviolet (UV) photobiology, plant cell wall biochemistry, aerobic methane production and reactive oxygen species (ROS) mechanisms to investigate the effect of UV radiation on vegetation foliage. Following reports of a 17% increase in decomposition rates in oak (Quercus robur) due to increased UV, which were later ascribed to changes in cell wall carbohydrate extractability, this study investigated the effects of decreased UV levels on ash (Fraxinus excelsior), a fast-growing deciduous tree species. A field experiment was set up in Surrey, UK, with ash seedlings growing under polytunnels made of plastics chosen for the selective transmission of either all UV wavelengths, UV-A only, or no UV. In a subsequent field decomposition experiment on end-of-season leaves, a significant increase of 10% in decomposition rate was found after one year due to removal of UV-B. However, no significant changes in cell wall composition were found, and a sequential extraction of carbohydrate with different extractants suggested no effects of the UV treatments on cell wall structure. Meanwhile, the first observations of aerobic production of methane from vegetation were reported. Pectin, a key cell wall polysaccharide, was identified as a putative source of methane, but no mechanism was suggested for this production. This study therefore tested the effect of UV irradiation on methane emissions from pectin. A linear response of methane emissions against UV irradiation was found. UV-irradiation of de-esterified pectin produced no methane, demonstrating esters (probably methyl esters) to be the source of the observed methane. Addition of ROS-scavengers significantly decreased emissions from pectin, while addition of ROS without UV produced large quantities of methane. Therefore, this study proposes that UV light is generating ROS which are then attacking methyl esters to create methane. The study also demonstrates that this mechanism has the potential to generate several types of methyl halides. These findings may have implications for the global methane budget. In an attempt to demonstrate ROS generation in vivo by UV irradiation, radio-labelling techniques were developed to detect the presence of oxo groups, a product of carbohydrate attack by ROS. Using NaB3H4, the polysaccharides of ash leaflets from the field experiment were radio-labelled, but did not show any significant decrease in oxo groups due to UV treatments. However, UV-irradiation of lettuce leaves showed a significant increase in radio-labelling, suggesting increased UV irradiation caused an increase in the production of ROS. The study shows that the use of this radio-labelling technique has the potential to detect changes in ROS production due to changes in UV levels and could be used to demonstrate a link between ROS levels and methane emissions.
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Dong, Wen. "Extensin Peroxidase Identification and Characterization in Solanum lycopersicum." Ohio University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1425894387.

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Pegg, Timothy Joseph. "Cell Wall Carbohydrate Modifications during Flooding-Induced Aerenchyma Formation in Fabaceae Roots." Miami University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1626443795433208.

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Wiemels, Richard E. "Cloning, Expression, and Biochemical Assay of Putative Xyloglucan-specific Fucosyltransferases from Wheat and Brachypodium." Ohio University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1368012677.

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Jiang, Nan. "Characterization of TaXPol-1, a Xylan Synthase Complex from Wheat." Ohio University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1437153132.

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Books on the topic "Plant cell wall biochemistry"

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K, Waldron, ed. Physiology and biochemistry of plant cell walls. London: Unwin Hyman, 1990.

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Brett, C., and K. Waldron. Physiology and Biochemistry of Plant Cell Walls. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6.

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W, Rowe John. Natural Products of Woody Plants: Chemicals Extraneous to the Lignocellulosic Cell Wall. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989.

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Linskens, Hans Ferdinand, and John F. Jackson, eds. Plant Cell Wall Analysis. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-60989-3.

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Popper, Zoë A., ed. The Plant Cell Wall. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-008-9.

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Popper, Zoë A., ed. The Plant Cell Wall. New York, NY: Springer New York, 2020. http://dx.doi.org/10.1007/978-1-0716-0621-6.

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Lewis, Norman G., and Michael G. Paice, eds. Plant Cell Wall Polymers. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0399.

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Fukuda, H. Plant cell wall patterning and cell shape. Hoboken, New Jersey: John Wiley & Sons Inc., 2015.

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Fukuda, Hiroo, ed. Plant Cell Wall Patterning and Cell Shape. Hoboken, NJ, USA: John Wiley & Sons, Inc, 2014. http://dx.doi.org/10.1002/9781118647363.

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König, Helmut. Prokaryotic Cell Wall Compounds: Structure and Biochemistry. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

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Book chapters on the topic "Plant cell wall biochemistry"

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Brett, C., and K. Waldron. "Cell-wall formation." In Physiology and Biochemistry of Plant Cell Walls, 58–88. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_3.

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Brett, C., and K. Waldron. "Cell-wall degradation." In Physiology and Biochemistry of Plant Cell Walls, 168–79. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_8.

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Brett, C., and K. Waldron. "The cell wall and reproduction." In Physiology and Biochemistry of Plant Cell Walls, 155–67. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_7.

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Brett, C., and K. Waldron. "Cell wall structure and the skeletal functions of the wall." In Physiology and Biochemistry of Plant Cell Walls, 4–57. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_2.

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Brett, C., and K. Waldron. "The cell wall and control of cell growth." In Physiology and Biochemistry of Plant Cell Walls, 89–113. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_4.

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Brett, C., and K. Waldron. "The cell wall and intercellular transport." In Physiology and Biochemistry of Plant Cell Walls, 114–36. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_5.

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Brett, C., and K. Waldron. "The cell wall and interactions with other organisms." In Physiology and Biochemistry of Plant Cell Walls, 137–54. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_6.

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Brett, C., and K. Waldron. "The role of the cell wall in the life of the plant." In Physiology and Biochemistry of Plant Cell Walls, 1–3. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_1.

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Brett, C., and K. Waldron. "Outstanding problems for future research." In Physiology and Biochemistry of Plant Cell Walls, 180–81. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6_9.

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Minic, Zoran, Georges Boudart, Cécile Albenne, Hervé Canut, Elisabeth Jamet, and Rafael F. Pont-Lezica. "Cell Wall Proteome." In Plant Proteomics, 169–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-72617-3_12.

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Conference papers on the topic "Plant cell wall biochemistry"

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Hojae Yi, Virendra M Puri, and M Shafayet Zamil. "Structure based Computational Plant Cell Wall Model." In 2012 Dallas, Texas, July 29 - August 1, 2012. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2012. http://dx.doi.org/10.13031/2013.42145.

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Bidhendi, Amir. "Live fluorescence labeling of the primary plant cell wall polysaccharides." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1374633.

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Guillon, F., C. Barron, B. Bouchet, M. F. Devaux, F. Jamme, S. Philppe, P. Robert, L. Saulnier, and O. Tranquet. "Organisation of Plant Cell Wall by Imaging Techniques." In 13th World Congress of Food Science & Technology. Les Ulis, France: EDP Sciences, 2006. http://dx.doi.org/10.1051/iufost:20061361.

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"Plant cell wall as a target for functional genomics." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Novosibirsk ICG SB RAS 2021, 2021. http://dx.doi.org/10.18699/plantgen2021-068.

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Zhuo Li and Justin R Barone. "Polyphenol-nanocellulose Composites that Biomimic the Plant Cell Wall." In 2009 Reno, Nevada, June 21 - June 24, 2009. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2009. http://dx.doi.org/10.13031/2013.27015.

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Chen, Liang-cai, Jin-ji Wang, Peng Ma, Du-luo Zuo, Xin-bing Wang, and Zu-hai Cheng. "Theoretical investigation on breaking plant cell wall by laser." In Photonics and Optoelectronics Meetings 2011, edited by Jianquan Yao, X. C. Zhang, Dapeng Yan, and Jinsong Liu. SPIE, 2012. http://dx.doi.org/10.1117/12.916284.

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Minami, Anzu. "CELL WALL INVERTASE4 controls nectar volume and sugar composition in Brassica rapa." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1052925.

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Pegg, Timothy J. "Immuprofiling of Cell Wall Carbohydrate Modifications during Aerenchyma Formation in Fabaceae Roots." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.989685.

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Mohammad Shafayet Zamil, Aman Haque, Hojae Yi, and Virendra M Puri. "A Device for Plant Cell Wall Testing in Tensile Loading." In 2012 Dallas, Texas, July 29 - August 1, 2012. St. Joseph, MI: American Society of Agricultural and Biological Engineers, 2012. http://dx.doi.org/10.13031/2013.42174.

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Choo, Tze Siang, Bjorn Usadel, and Markus Pauly. "PLANT CELL WALL OLIGOSACCHARIDES PROFILING USING MALDI-TOF MASS SPECTROMETRY." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.718.

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Reports on the topic "Plant cell wall biochemistry"

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Varner, J. (Hydroxyproline-rich glycoproteins of the plant cell wall). Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6855639.

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Varner, J. E. [Hydroxyproline: Rich glycoproteins of the plant and cell wall]. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/6806611.

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Cosgrove, D. (Rapid regulatory control of plant cell expansion and wall relaxation). Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/5080397.

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Cosgrove, D. J. Rapid regulatory control of plant cell expansion and wall relaxation. Office of Scientific and Technical Information (OSTI), August 1991. http://dx.doi.org/10.2172/5217091.

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Hazen, Samuel. Systems Level Engineering of Plant Cell Wall Biosynthesis to Improve Biofuel Feedstock Quality. Office of Scientific and Technical Information (OSTI), September 2013. http://dx.doi.org/10.2172/1094975.

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Nielsen, Erik Etlar. Investigation of the functional role of CSLD proteins in plant cell wall deposition. Office of Scientific and Technical Information (OSTI), November 2017. http://dx.doi.org/10.2172/1409677.

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David B. Wilson. IDENTIFICATION AND CHARACTERIZATION OF THERMOBIFIDA FUSCA GENES INVOLVED IN PLANT CELL WALL DEGRADATION. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/862421.

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Author, Not Given. Plant cell wall architecture. Final technical report for DOE award no. DE-FG02-97ER20258. Office of Scientific and Technical Information (OSTI), August 2002. http://dx.doi.org/10.2172/807344.

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Azadi, Paratoo. 8th Annual Glycoscience Symposium: Integrating Models of Plant Cell Wall Structure, Biosynthesis and Assembly. Office of Scientific and Technical Information (OSTI), September 2015. http://dx.doi.org/10.2172/1221374.

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Varner, J. E. [Hydroxyproline: Rich glycoproteins of the plant and cell wall]. Annual technical progress report, 1993. Office of Scientific and Technical Information (OSTI), June 1993. http://dx.doi.org/10.2172/10156257.

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