Academic literature on the topic 'Wool proteomics'

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Wool proteomics.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Wool proteomics"

1

Plowman, Jeffrey E., Duane P. Harland, Sivasangary Ganeshan, Joy L. Woods, Bede van Shaijik, Santanu Deb-Choudhury, Ancy Thomas, Stefan Clerens, and David R. Scobie. "The proteomics of wool fibre morphogenesis." Journal of Structural Biology 191, no. 3 (September 2015): 341–51. http://dx.doi.org/10.1016/j.jsb.2015.07.005.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Plowman, Jeffrey E., Warren G. Bryson, and T. William Jordan. "Application of proteomics for determining protein markers for wool quality traits." Electrophoresis 21, no. 9 (May 1, 2000): 1899–906. http://dx.doi.org/10.1002/(sici)1522-2683(20000501)21:9<1899::aid-elps1899>3.0.co;2-r.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Solazzo, Caroline, Stefan Clerens, Jeffrey E. Plowman, Julie Wilson, Elizabeth E. Peacock, and Jolon M. Dyer. "Application of redox proteomics to the study of oxidative degradation products in archaeological wool." Journal of Cultural Heritage 16, no. 6 (November 2015): 896–903. http://dx.doi.org/10.1016/j.culher.2015.02.006.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Guo, Tingting, Jilong Han, Chao Yuan, Jianbin Liu, Chune Niu, Zengkui Lu, Yaojing Yue, and Bohui Yang. "Comparative proteomics reveals genetic mechanisms underlying secondary hair follicle development in fine wool sheep during the fetal stage." Journal of Proteomics 223 (July 2020): 103827. http://dx.doi.org/10.1016/j.jprot.2020.103827.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Rogers, George E. "Known and Unknown Features of Hair Cuticle Structure: A Brief Review." Cosmetics 6, no. 2 (May 9, 2019): 32. http://dx.doi.org/10.3390/cosmetics6020032.

Full text
Abstract:
The cuticle is the outermost layer of overlapping flattened cells of hair and has been subjected to many years of study to understand its structure and how it develops in the follicle. The essential function of the cuticle with its tough inelastic protein content is to protect the inner cortex that provides the elastic properties of hair. Progress in our knowledge of hair came from studies with the electron microscope, initially transmission electron microscopy (TEM) for internal structure and later the scanning electron microscope (SEM) for cuticle surface shape and for investigating changes caused by various environmental influences such as cosmetic treatments and industrial processing of wool. Other physical techniques have been successfully applied in conjunction with proteomics. The outstanding internal features of the cuticle cells are the internal layers consisting of keratin filament proteins and the keratin-associated proteins. The stability and physical toughness of the cuticle cell is partly accounted for by the high content of disulphide crosslinking. The material between the cells that holds them tightly together, the cell membrane complex, consists of a layer of lipid on both sides of a central protein layer. The lipid contains 18-methyleicosanoic acid that is part of the hydrophobic lipid surface of hair. For the past decade there have been aspects that remained unanswered because they are difficult to study. Some of these are discussed in this brief review with suggestions for experimental approaches to shed more light.
APA, Harvard, Vancouver, ISO, and other styles
6

PLOWMAN, J. "Proteomic database of wool components." Journal of Chromatography B 787, no. 1 (April 5, 2003): 63–76. http://dx.doi.org/10.1016/s1570-0232(02)00211-8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Plowman, Jeffrey E., Joy L. Woods, Bede van Schaijik, and Duane P. Harland. "Preparation of wool follicles for proteomic studies." Analytical Biochemistry 539 (December 2017): 8–10. http://dx.doi.org/10.1016/j.ab.2017.08.020.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Oosthuizen, Marinda C., Bridgitta Steyn, Jacques Theron, Pascal Cosette, Denise Lindsay, Alexander von Holy, and Volker S. Brözel. "Proteomic Analysis Reveals Differential Protein Expression by Bacillus cereus during Biofilm Formation." Applied and Environmental Microbiology 68, no. 6 (June 2002): 2770–80. http://dx.doi.org/10.1128/aem.68.6.2770-2780.2002.

Full text
Abstract:
ABSTRACT Bacillus cereus, a dairy-associated toxigenic bacterium, readily forms biofilms on various surfaces and was used to gain a better understanding of biofilm development by gram-positive aerobic rods. B. cereus DL5 was shown to readily adapt to an attached mode of growth, with dense biofilm structures developing within 18 h after inoculation when glass wool was used as a surface. Two-dimensional gel electrophoresis (2DE) revealed distinct and reproducible phenotypic differences between 2- and 18-h-old biofilm and planktonic cells (grown both in the presence and in the absence of glass wool). Whereas the 2-h-old biofilm proteome indicated expression of 15 unique proteins, the 18-h-old biofilm proteome contained 7 uniquely expressed proteins. Differences between the microcolony (2-h) proteome and the more developed biofilm (18-h) proteome were largely due to up- and down-regulation of the expression of a multitude of proteins. Selected protein spots excised from 2DE gels were subjected to N-terminal sequencing and identified with high confidence. Among the proteins were catabolic ornithine carbamoyltransferase and l-lactate dehydrogenase. Interestingly, increased levels of YhbH, a member of the sigma 54 modulation protein family which is strongly induced in response to environmental stresses and energy depletion via both σB and σH, could be observed within 2 h in both attached cells and planktonic cultures growing in the presence of glass wool, indicating that this protein plays an important role in regulation of the biofilm phenotype. Distinct band differences were also found between the extracellular proteins of 18-h-old cultures grown in the presence and in the absence of glass wool.
APA, Harvard, Vancouver, ISO, and other styles
9

Dyer, Jolon M., Jeff E. Plowman, Gail L. Krsinic, Santanu Deb-Choudhury, Henning Koehn, Keith R. Millington, and Stefan Clerens. "Proteomic evaluation and location of UVB-induced photo-oxidation in wool." Journal of Photochemistry and Photobiology B: Biology 98, no. 2 (February 2010): 118–27. http://dx.doi.org/10.1016/j.jphotobiol.2009.11.008.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Solazzo, Caroline, Jolon M. Dyer, Stefan Clerens, Jeff Plowman, Elizabeth E. Peacock, and Matthew J. Collins. "Proteomic evaluation of the biodegradation of wool fabrics in experimental burials." International Biodeterioration & Biodegradation 80 (May 2013): 48–59. http://dx.doi.org/10.1016/j.ibiod.2012.11.013.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Wool proteomics"

1

Pizol, José Vitor. "The effects of rockrose extract feed inclusion on the wool proteome of portuguese White Merinos." Master's thesis, ISA, 2020. http://hdl.handle.net/10400.5/21503.

Full text
Abstract:
Mestrado em Engenharia Zootécnica - Produção Animal / Instituto Superior de Agronomia / Faculdade de Medicina Veterinária. Universidade de Lisboa
This study was carried out with the objective of evaluating the effect of feeding extract of rockrose (Cistus ladanifer L.), a perennial shrub commonly found in the marginal regions of Portugal and rich in condensed tannins (CT), and its effect on the wool proteome of Portuguese White Merinos. Twenty-four Portuguese White Merinos lambs were fed a diet restricted in protein and composed of grass hay (15%) and concentrate (85%), where they were distributed in three experimental groups: control group, composed of 16% crude protein (CP); diet restricted to 12% crude protein (RP) and diet restricted to 12% crude protein and treated with 1.5% rockrose extract (RPCT). After the 5-week experimental period, samples of wool present in an area of approximately 100cm² in the anterior region of the head were collected from each animal and used for subsequent analysis of proteomics based on liquid chromatography - mass spectrometry (LC-MS). The proteomic method identified 110 proteins in the wool fibre. Of this total, 4 showed significance (P<0.05) and could be classified as structural proteins, with three Type I keratins (Keratin 36, Keratin Type I and Keratin 10) and one Keratin Associated Protein (KAP9.2). The differential accumulation results showed that the RPCT group decreased the expression of these proteins in relation to the Control and RP groups. Except for the K36 protein, which had a 19% higher expression for the RPCT group compared to the other two groups. We conclude that the rockrose extract has a minor effect on the wool proteome that affect specifically the parts of the wool fibre where these proteins are located with putative changes in fibre structure and properties. Finally, further microscopy and wool quality traits studies are still needed to confirm and explain these changes
N/A
APA, Harvard, Vancouver, ISO, and other styles
2

Garcés, Cea Marcelo Arnoldo Plomion Christophe. "Proteomic study of wood formation in maritime pine." S. l. : Bordeaux 1, 2008. http://ori-oai.u-bordeaux1.fr/pdf/2008/GARCES_CEA_MARCELO_2008.pdf.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Garcés, Cea Marcelo Arnoldo. "Proteomic study of wood formation in maritime pine." Thesis, Bordeaux 1, 2008. http://www.theses.fr/2008BOR13633/document.

Full text
Abstract:
Les propriétés du bois de pin maritime varient aux niveaux chimique, anatomique et mécanique. Six types de bois peuvent être trouvés au sein d’un même arbre : bois précoce, bois tardif, bois de couronne, bois de base, bois de compression et bois opposé. Au cours de cette thèse, nous avons testé l’hypothèse selon laquelle la variabilité phénotypique des propriétés de bois, serait liée à l’expression différentielle des protéines lors de la xylogénèse. Par une approche protéomique basée sur l’électrophorèse bidimensionnelle et la spectrométrie de masse en tandem (LC ESI MS/MS), nous avons identifié 165 protéines différentiellement exprimées le long d’un gradient d’âge cambial (bois juvénile vs. bois mature) ainsi que 93 protéines différentiellement exprimées au cours de la saison de végétation (bois de printemps vs. bois d’été) chez le pin maritime. Une analyse chimique complémentaire des échantillons a été réalisée par pyrolyse analytique. Nos résultats montrent que le xylème secondaire formé en début de saison ainsi que celui qui est initié par un cambium jeune présentent une sur-expression de protéines participant à la division cellulaire. Dans le xylème issu d’un cambium âgé ou formé à la fin de l’été nous avons mis en évidence des protéines impliquées dans la défense cellulaire (dont le rôle serait de retarder la mort cellulaire programmée), ainsi que des protéines impliqués dans la biosynthèse des éléments constitutifs de la paroi. Cette étude contribue à renforcer nos connaissances sur les acteurs moléculaires intervenant lors de la xylogénèse. Elle ouvre par ailleurs des pistes de recherche sur la détection de gènes impliqués dans le contrôle génétique des propriétés du bois dans un objectif de sélection assisté par marqueurs
Wood properties in maritime pine are highly variable at chemical, anatomical and mechanical levels. Six types of wood can be found in a single tree, early wood, late wood, crown wood, base wood, compression wood and opposite wood. In this thesis report, we tested the hypothesis that the observed variability at the phenotypic level, can be bound to the differential expression of proteins during the process of wood formation. We use the tools of proteomics, Bidimensional electrophoresis and LC ESI MS/MS for the discovery of 165 proteins differentially expressed in a cambial age gradient, (from base wood to crown wood), an 93 overexpressed proteins in a seasonal gradient (from early wood collected at the beginning of the growing season, to late wood, collected at summer) Complementary, chemical characterization of the samples was performed using analitycal pyrolisis. Our results showed that the secondary xylem formed at the beginning of the growing season, and the xylem formed by a young cambium, present a overexpression of proteins participating in the intense cell division, characteristical of those tissues, e.g. Biogenesis of cytoskeleton and hemicelluloses, RNA transcription, synthesis, folding and modification of proteins. In the xylem formed at the base of the trunk and at the end of the growing season we have found an over-expression of proteins from cell defense (they role will be to delay programmed cell death) and cell wall formation related proteins e.g. lignin biosynthesis. This study contributes to reinforce our knowledge over the molecular actors involved in the xylogenesis process. It opens, in another hand , research guides for the detection of genes involved in the genetic control of wood properties towards an objecive of marker assisted selection
APA, Harvard, Vancouver, ISO, and other styles
4

Mahajan, Sonam. "Characterization of the White-rot Fungus, Phanerochaete carnosa, through Proteomic Methods and Compositional Analysis of Decayed Wood FibreCharacterization of the White-rot Fungus, Phanerochaete carnosa, through Proteomic Methods and Compositional Analysis of Decayed Wood Fibre." Thesis, 2011. http://hdl.handle.net/1807/31852.

Full text
Abstract:
Biocatalysts are important tools for harnessing the potential of wood fibres since they can perform specific reactions with low environmental impact. Challenges to bioconversion technologies as applied to wood fibres include low accessibility of plant cell wall polymers and the heterogeneity of plant cell walls, which makes it difficult to predict conversion efficiencies. White-rot fungi are among the most efficient degraders of plant fibre (lignocellulose), capable of degrading cellulose, hemicellulose and lignin. Phanerochaete carnosa is a white-rot fungus that, in contrast to many white-rot fungi that have been studied to date, was isolated almost exclusively from fallen coniferous trees (softwood). While several studies describe the lignocellulolytic activity of the hardwood-degrading, model white-rot fungus Phanerochaete chrysosporium, the lignocellulolytic activity of P. carnosa has not been investigated. An underlying hypothesis of this thesis is that P. carnosa encodes enzymes that are particularly well suited for processing softwood fibre, which is an especially recalcitrant feedstock, though a major resource for Canada. Moreover, given the phylogenetic similarity of P. carnosa and P. chrysosporium, it is anticipated that the identification of pertinent enzymes for softwood degradation can be more easily conducted. In particular, this project describes the characterization of P. carnosa in terms of the growth conditions that support lignocellulolytic activity, the effect of enzymes secreted by P. carnosa on the chemistry of softwood feedstocks, and the characterization of the corresponding secretome using proteomic techniques. Through this study, cultivation methods for P. carnosa were established and biochemical assays for protein activity and quantification were developed. Analytical methods, including FTIR and ToF-SIMS were used to characterize wood samples at advancing stages of decay, and revealed preferential degradation of lignin in the early stages of growth on all softwoods analyzed. Finally, an in depth proteomic analysis of the proteins secreted by P. carnosa on spruce and cellulose established that similar sets of enzyme activities are elicited by P. carnosa grown on different lignocellulosic substrates, albeit to different expression levels.
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Wool proteomics"

1

Plowman, Jeffrey E., and Santanu Deb-Choudhury. "Wool Proteomics." In Agricultural Proteomics Volume 1, 211–23. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43275-5_11.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Plowman, Jeffrey E., Sivasangary Ganeshan, Joy L. Woods, Santanu Deb-Choudhury, David R. Scobie, and Duane P. Harland. "The proteomics of wool follicles." In Farm animal proteomics 2013, 242–44. Wageningen: Wageningen Academic Publishers, 2013. http://dx.doi.org/10.3920/978-90-8686-776-9_61.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Plowman, Jeffrey E. "Proteomics in Wool and Fibre Research." In Proteomics in Domestic Animals: from Farm to Systems Biology, 281–96. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-69682-9_14.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

"Proteomic Analysis of Extracellular Enzymes Produced by Wood-Degrading Fungi." In Manual of Environmental Microbiology, Third Edition, 1089–96. American Society of Microbiology, 2007. http://dx.doi.org/10.1128/9781555815882.ch87.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography