Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:( PNAG). Showing records 1 – 8 of 8 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of Toronto

1. Chibba, Anthony. Substrates and Inhibitors of Enzymes Involved in Exopolysaccharide Dependent Biofilms.

Degree: PhD, 2014, University of Toronto

 Many biofilm-forming bacteria produce a similar partially de-N-acetylated β-1,6-N-acetyl glucosamine homopolymer (dPNAG) to facilitate bacterial adhesion. In many medically important biofilm forming bacterial strains, including… (more)

Subjects/Keywords: Biofilms; Carbohydrate; Chemoenzymatic; PNAG; 0490

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chibba, A. (2014). Substrates and Inhibitors of Enzymes Involved in Exopolysaccharide Dependent Biofilms. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68263

Chicago Manual of Style (16th Edition):

Chibba, Anthony. “Substrates and Inhibitors of Enzymes Involved in Exopolysaccharide Dependent Biofilms.” 2014. Doctoral Dissertation, University of Toronto. Accessed June 16, 2019. http://hdl.handle.net/1807/68263.

MLA Handbook (7th Edition):

Chibba, Anthony. “Substrates and Inhibitors of Enzymes Involved in Exopolysaccharide Dependent Biofilms.” 2014. Web. 16 Jun 2019.

Vancouver:

Chibba A. Substrates and Inhibitors of Enzymes Involved in Exopolysaccharide Dependent Biofilms. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1807/68263.

Council of Science Editors:

Chibba A. Substrates and Inhibitors of Enzymes Involved in Exopolysaccharide Dependent Biofilms. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68263


University of Toronto

2. Kawase, Yoshiyuki Alexander. Molecular Mechanisms Of Chain Elongation, A Fundamental Process In Bacterial Biofilm Formation.

Degree: 2013, University of Toronto

Biofilm formation, the agglomeration of microorganisms on a surface, can account for greater than 80% of all human microbial infections. In a large group of… (more)

Subjects/Keywords: Biofilm formation; glycosyl transferases; PIA; PNAG; 0487

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kawase, Y. A. (2013). Molecular Mechanisms Of Chain Elongation, A Fundamental Process In Bacterial Biofilm Formation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69765

Chicago Manual of Style (16th Edition):

Kawase, Yoshiyuki Alexander. “Molecular Mechanisms Of Chain Elongation, A Fundamental Process In Bacterial Biofilm Formation.” 2013. Masters Thesis, University of Toronto. Accessed June 16, 2019. http://hdl.handle.net/1807/69765.

MLA Handbook (7th Edition):

Kawase, Yoshiyuki Alexander. “Molecular Mechanisms Of Chain Elongation, A Fundamental Process In Bacterial Biofilm Formation.” 2013. Web. 16 Jun 2019.

Vancouver:

Kawase YA. Molecular Mechanisms Of Chain Elongation, A Fundamental Process In Bacterial Biofilm Formation. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1807/69765.

Council of Science Editors:

Kawase YA. Molecular Mechanisms Of Chain Elongation, A Fundamental Process In Bacterial Biofilm Formation. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/69765


Virginia Commonwealth University

3. Brooks, Jamie. Characterization of the expression of the intercellular adhesin locus in Staphylococcus aureus.

Degree: PhD, Microbiology & Immunology, 2012, Virginia Commonwealth University

 Poly-N-acetylglucosamine (PNAG) is an important Staphylococcus aureus virulence factor. It is a major component of the extracellular polymeric matrix in biofilms, and contributes to resistance… (more)

Subjects/Keywords: Staphylococcus aureus; icaADBC; ica; PNAG; Medicine and Health Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Brooks, J. (2012). Characterization of the expression of the intercellular adhesin locus in Staphylococcus aureus. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2934

Chicago Manual of Style (16th Edition):

Brooks, Jamie. “Characterization of the expression of the intercellular adhesin locus in Staphylococcus aureus.” 2012. Doctoral Dissertation, Virginia Commonwealth University. Accessed June 16, 2019. https://scholarscompass.vcu.edu/etd/2934.

MLA Handbook (7th Edition):

Brooks, Jamie. “Characterization of the expression of the intercellular adhesin locus in Staphylococcus aureus.” 2012. Web. 16 Jun 2019.

Vancouver:

Brooks J. Characterization of the expression of the intercellular adhesin locus in Staphylococcus aureus. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2012. [cited 2019 Jun 16]. Available from: https://scholarscompass.vcu.edu/etd/2934.

Council of Science Editors:

Brooks J. Characterization of the expression of the intercellular adhesin locus in Staphylococcus aureus. [Doctoral Dissertation]. Virginia Commonwealth University; 2012. Available from: https://scholarscompass.vcu.edu/etd/2934


Cornell University

4. Stevenson, Taylor Currie. ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES .

Degree: 2017, Cornell University

 The use of vaccines has led to the effective eradication of several human diseases which were once epidemic such as smallpox and polio. Vaccines have… (more)

Subjects/Keywords: Chemical engineering; Biomedical engineering; glycobiolology; glycoconjugate; OMV; PNAG; polysaccharide; vaccine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Stevenson, T. C. (2017). ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/47799

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Stevenson, Taylor Currie. “ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES .” 2017. Thesis, Cornell University. Accessed June 16, 2019. http://hdl.handle.net/1813/47799.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Stevenson, Taylor Currie. “ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES .” 2017. Web. 16 Jun 2019.

Vancouver:

Stevenson TC. ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES . [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1813/47799.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Stevenson TC. ENGINEERING BACTERIAL GLYCOBIOLOGY FOR THE CREATION OF GLYCOCONJUGATE VACCINES . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47799

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas A&M University

5. Rocha, Joana Nunes. Antibodies Targeting Poly-N-Acetyl Glucosamine Protect Against the Intracellular Pathogen, Rhodococcus Equi.

Degree: PhD, Biomedical Sciences, 2018, Texas A&M University

 Rhodococcus equi is a facultative intracellular pathogen that causes pyogranulomatous pneumonia in foals <6 months of age. Why foals are highly susceptible to R. equi… (more)

Subjects/Keywords: Rhodococcus equi; PNAG; Vaccine; IgG subisotypes; functional mechanisms

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rocha, J. N. (2018). Antibodies Targeting Poly-N-Acetyl Glucosamine Protect Against the Intracellular Pathogen, Rhodococcus Equi. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174337

Chicago Manual of Style (16th Edition):

Rocha, Joana Nunes. “Antibodies Targeting Poly-N-Acetyl Glucosamine Protect Against the Intracellular Pathogen, Rhodococcus Equi.” 2018. Doctoral Dissertation, Texas A&M University. Accessed June 16, 2019. http://hdl.handle.net/1969.1/174337.

MLA Handbook (7th Edition):

Rocha, Joana Nunes. “Antibodies Targeting Poly-N-Acetyl Glucosamine Protect Against the Intracellular Pathogen, Rhodococcus Equi.” 2018. Web. 16 Jun 2019.

Vancouver:

Rocha JN. Antibodies Targeting Poly-N-Acetyl Glucosamine Protect Against the Intracellular Pathogen, Rhodococcus Equi. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1969.1/174337.

Council of Science Editors:

Rocha JN. Antibodies Targeting Poly-N-Acetyl Glucosamine Protect Against the Intracellular Pathogen, Rhodococcus Equi. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/174337


University of Toronto

6. DiFrancesco, Benjamin Robert. The Development of Substrates and Inhibitors of the PNAG Biosynthetic Machinery.

Degree: PhD, 2018, University of Toronto

 Biofilms are surface-attached colonies of bacteria that are encapsulated in an extracellular matrix composed of a milieu of proteins, nucleic acids and polysaccharides. In a… (more)

Subjects/Keywords: Assay Development; Biofilms; Deacetylase; Drug Design; Enzymology; PNAG; 0485

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

DiFrancesco, B. R. (2018). The Development of Substrates and Inhibitors of the PNAG Biosynthetic Machinery. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/91837

Chicago Manual of Style (16th Edition):

DiFrancesco, Benjamin Robert. “The Development of Substrates and Inhibitors of the PNAG Biosynthetic Machinery.” 2018. Doctoral Dissertation, University of Toronto. Accessed June 16, 2019. http://hdl.handle.net/1807/91837.

MLA Handbook (7th Edition):

DiFrancesco, Benjamin Robert. “The Development of Substrates and Inhibitors of the PNAG Biosynthetic Machinery.” 2018. Web. 16 Jun 2019.

Vancouver:

DiFrancesco BR. The Development of Substrates and Inhibitors of the PNAG Biosynthetic Machinery. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1807/91837.

Council of Science Editors:

DiFrancesco BR. The Development of Substrates and Inhibitors of the PNAG Biosynthetic Machinery. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91837

7. Poloczek, Joanna. Biochemical Characterization of Escherichia coli PgaB, an Enzyme Essential for Biofilm Formation.

Degree: 2012, University of Toronto

The formation of bacterial biofilms requires an extracellular matrix to facilitate adherence of bacteria to the surface they colonize. Carbohydrate polymers, known as exopolysaccharides, form… (more)

Subjects/Keywords: PNAG; deacetylase; biofilm; polysaccharide intercellular adhesin; 0487

…10 Figure 1.5 Structural representation of PNAG matrix polysaccharide… …13 Figure 1.7 Model of PNAG synthesis, as proposed by Itoh et al.(75)… …iron ... 32 ix Figure 3.1 MALDI-MS spectrum of PgaB-treated PNAG pentasaccharide… …56 Figure 3.12 Deacetylation positions of PNAG pentaccharide as determined from… …59 Figure 3.13 Deacetylation positions of di-de-N-acetylated PNAG hexasaccharide as… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Poloczek, J. (2012). Biochemical Characterization of Escherichia coli PgaB, an Enzyme Essential for Biofilm Formation. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/65488

Chicago Manual of Style (16th Edition):

Poloczek, Joanna. “Biochemical Characterization of Escherichia coli PgaB, an Enzyme Essential for Biofilm Formation.” 2012. Doctoral Dissertation, University of Toronto. Accessed June 16, 2019. http://hdl.handle.net/1807/65488.

MLA Handbook (7th Edition):

Poloczek, Joanna. “Biochemical Characterization of Escherichia coli PgaB, an Enzyme Essential for Biofilm Formation.” 2012. Web. 16 Jun 2019.

Vancouver:

Poloczek J. Biochemical Characterization of Escherichia coli PgaB, an Enzyme Essential for Biofilm Formation. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1807/65488.

Council of Science Editors:

Poloczek J. Biochemical Characterization of Escherichia coli PgaB, an Enzyme Essential for Biofilm Formation. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/65488


Leiden University

8. Dissel, van, M.D. Exploring and exploiting the mechanism of mycelial pellet formation by Streptomyces.

Degree: 2016, Leiden University

 Streptomyces are multicellular bacteria that grow as branched filaments and are best known for producing the majority of our antibiotics, many immunosuppressant and anticancer compounds.… (more)

Subjects/Keywords: Streptomyces; Poly-1,6-N-acetylglucosamine; PNAG; Aggregation; Biofilm formation; Antibiotics; Morphology; Streptomyces; Poly-1,6-N-acetylglucosamine; PNAG; Aggregation; Biofilm formation; Antibiotics; Morphology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Dissel, van, M. D. (2016). Exploring and exploiting the mechanism of mycelial pellet formation by Streptomyces. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/44777

Chicago Manual of Style (16th Edition):

Dissel, van, M D. “Exploring and exploiting the mechanism of mycelial pellet formation by Streptomyces.” 2016. Doctoral Dissertation, Leiden University. Accessed June 16, 2019. http://hdl.handle.net/1887/44777.

MLA Handbook (7th Edition):

Dissel, van, M D. “Exploring and exploiting the mechanism of mycelial pellet formation by Streptomyces.” 2016. Web. 16 Jun 2019.

Vancouver:

Dissel, van MD. Exploring and exploiting the mechanism of mycelial pellet formation by Streptomyces. [Internet] [Doctoral dissertation]. Leiden University; 2016. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/1887/44777.

Council of Science Editors:

Dissel, van MD. Exploring and exploiting the mechanism of mycelial pellet formation by Streptomyces. [Doctoral Dissertation]. Leiden University; 2016. Available from: http://hdl.handle.net/1887/44777

.