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Elizabeth J. Skellam

Title: Assistant Professor

Department: Chemistry

College: College of Science

Curriculum Vitae

Curriculum Vitae Link

Education

  • MBA, University of North Carolina at Wilmington, 2013
    Major: Biotechnology
  • PhD, University of Bristol, 2010
    Major: Chemistry
    Dissertation: Investigating the Programming of Fungal Tetraketide Synthases'
  • MSc, University of Wales Swansea, 2005
    Major: Chemistry

Current Scheduled Teaching

No current or future courses scheduled.

Previous Scheduled Teaching

BIOL 4951.730Honors College Capstone ThesisSpring 2024
CHEM 6940.762Individual ResearchSpring 2024
CHEM 5950.776Master's ThesisSpring 2024
CHEM 4930.002Selected Topics in ChemistrySpring 2024 Syllabus SPOT
CHEM 5640.001Selected Topics in Organic ChemistrySpring 2024 SPOT
CHEM 6010.776Seminar for Doctoral CandidatesSpring 2024
BIOC 6900.730Special ProblemsSpring 8W1 2024
CHEM 4900.712Special ProblemsSpring 2024
CHEM 3996.712Honors College Mentored Research ExperienceFall 2023
CHEM 6940.762Individual ResearchFall 2023
CHEM 2900.712Introduction to Chemical ResearchFall 2023
CHEM 2370.003Organic Chemistry IFall 2023 Syllabus SPOT
CHEM 2370.203Organic Chemistry IFall 2023 SPOT
CHEM 4900.712Special ProblemsFall 2023
BIOL 3996.730Honors College Mentored Research ExperienceSummer 10W 2023
BIOL 4900.730Special ProblemsSummer 5W2 2023
CHEM 6940.762Individual ResearchSpring 2023
CHEM 2900.712Introduction to Chemical ResearchSpring 2023
CHEM 5640.001Selected Topics in Organic ChemistrySpring 2023 SPOT
BIOL 4900.730Special ProblemsSpring 2023
CHEM 4900.712Special ProblemsSpring 2023
CHEM 6940.762Individual ResearchFall 2022
CHEM 2900.712Introduction to Chemical ResearchFall 2022
CHEM 2370.002Organic ChemistryFall 2022 Syllabus SPOT
CHEM 2370.202Organic ChemistryFall 2022
CHEM 4900.712Special ProblemsFall 2022
CHEM 6940.762Individual ResearchSpring 2022
CHEM 2900.712Introduction to Chemical ResearchSpring 2022
CHEM 2370.001Organic ChemistrySpring 2022 Syllabus SPOT
CHEM 2370.211Organic ChemistrySpring 2022
CHEM 4900.712Special ProblemsSpring 2022
CHEM 6940.762Individual ResearchFall 2021
CHEM 2900.712Introduction to Chemical ResearchFall 2021
CHEM 4900.712Special ProblemsFall 2021
CHEM 2900.712Introduction to Chemical ResearchSummer 10W 2021
CHEM 2900.712Introduction to Chemical ResearchSpring 2021
CHEM 4930.002Selected Topics in ChemistrySpring 2021 SPOT
CHEM 5640.001Selected Topics in Organic ChemistrySpring 2021 Syllabus SPOT
CHEM 4900.712Special ProblemsSpring 2021 Syllabus

Published Intellectual Contributions

    Book

  • Skellam, E. (2022). Methods in Molecular Biology: Engineering Natural Products Biosynthesis. 2489 Springer Nature. https://link.springer.com/book/9781071622728
  • Book Chapter

  • Skellam, E. (2021). Analysis of the secondary metabolism in Magnaporthe oryzae. Methods in Molecular Biology: Magnaporthe.
  • Cox, R., Skellam, E. (2020). 1.09 Fungal Non-Reducing Polyketide Synthases. Comprehensive Natural Products III. https://books.google.com/books?hl=en&lr=&id=xXHhDwAAQBAJ&oi=fnd&pg=PA266&ots=Egc1U2N61r&sig=bO7YvGQG9pBfa-dhK1EL57D7Bao#v=onepage&q&f=false
  • Cox, R., Skellam, E., Williams, K. (2018). Biosynthesis of fungal polyketides. The Mycota -,Physiology and,Genetics XV.
  • Journal Article

  • Skellam, E. (2022). Subcellular compartmentalization of fungal biosynthetic enzymes. 9 Springer Link. https://link.springer.com/article/10.1186/s40694-022-00140-z
  • Shenouda, M., Ambilika, M., Skellam, E.J., Cox, R.J. (2022). Heterologous Expression of Secondary Metabolite Genes in Trichoderma reesei for Waste Valorization.
  • Kahlert, L., Villanueva, M., Cox, R., Skellam, E. Biosynthesis of 6-Hydroxymellein Requires a Collaborating Polyketide Synthase-like Enzyme. Angewandte Chemie International Edition. 60 (20) 11423-11429. https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202100969
  • Feng, J., hauser, m., Cox, R., Skellam, E. (2021). Engineering Aspergillus oryzae for the Heterologous Expression of a Bacterial Modular Polyketide Synthase. 7 (12) MPDI. https://www.mdpi.com/2309-608X/7/12/1085
  • Skellam, E.J. (2021). Biosynthesis of fungal polyketides by collaborating and trans-acting enzymes. 39 RSC. https://pubs.rsc.org/en/content/articlelanding/2022/np/d1np00056j/unauth
  • Kahlert, L., Bernardi, D., Hauser, M., Ioca, L., Berlinck, R., Skellam, E., Cox, R. (2021). Early Oxidative Transformations During the Biosynthesis of Terrein and Related Natural Products. 27 (46) 11895-11903. Wiley. https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202101447
  • Zhang, H., Hantke, V., Brunhke, P., Skellam, E., Cox, R. (2020). Chemical and Genetic Studies on the Formation of Pyrrolones During the Biosynthesis of Cytochalasans. Chemistry: A European Journal.
  • Kahlert, L., Cox, R., Skellam, E. (2020). The Same but Different: Multiple Functions of the Fungal Flavin Dependent Monooxygenase SorD from Penicillium chrysogenum. Chemical Communications. 56 10934-10937.
  • Wang, C., Lambert, C., Hauser, M., Deuschmann, A., Zeilinger, C., Stradal, T., Rottner, K., Stadler, M., Skellam, E., Cox, R. (2020). Diversely functionalised cytochalasins via mutasynthesis and semi-synthesis. Chemistry: A European Journal. 26 (60) 13578-13583.
  • Kahlert, L., Bassiony, E., Cox, R., Skellam, E. (2020). Diels-Alder reactions during the biosynthesis of sorbicillinoids. Angewandte Chemie International Edition. 59 (14) 5816-5822.
  • Hantke, V., Skellam, E., Cox, R. (2020). Evidence for Enzyme Catalysed Intramolecular [4+2] Diels-Alder Cyclization During the Biosynthesis of Pyrichalasin H. Chemical Communications. 56 2925-2928.
  • Hantke, V., Wang, C., Skellam, E., Cox, R. (2019). Function of pathway specific regulators in the ACE1 and pyrichalasin H biosynthetic gene clusters. RSC Advances. 9 35797-35802.
  • Wang, C., Becker, K., Pfuetze, S., Kuhnert, E., Stadler, M., Cox, R., Skellam, E. (2019). Investigating the Function of Cryptic Cytochalasan Cytochrome P450 Monooxygenases Using Combinatorial Biosynthesis. Organic Letters. 21 (21) 8756–8760.
  • Wang, C., Hantke, V., Cox, R., Skellam, E. (2019). Targeted gene inactivations expose silent cytochalasans in Magnaporthe grisea NI980. Organic Letters. 21 (11) 4163–4167. ACS.
  • Skellam, E. (2019). Strategies for engineering natural product biosynthesis in fungi. Trends in Biotechnology. 37 (4) 416-427.
  • Skellam, E. (2017). The biosynthesis of cytochalasans. 343 1252-1263. RSC.
  • Song, Z., Bakeer, W., Marshall, J., Yakasai, A., Khalid, R., Collemare, J., Skellam, E., Therreau, D., Lebrun, M., Lazarus, C., Bailey, A., Simpson, T., Cox, R. (2015). Heterologous expression of the avirulence gene ACE1 from the fungal rice pathogen Magnaporthe oryzae. Chemical Science. 6 4837-4845.
  • Skellam, E., Stewart, A., Strangman, W., Wright, J. (2013). Identification of micromonolactam, a new polyene lactam from two marine Micromonospora strains using chemical and molecular methods: Clarification of the biosynthetic pathway from a glutamate starter unit.
  • Fisch, K., Skellam, E., Ivson, D., Cox, R., Bailey, A., Lazarus, C., Simpson, T. (2010). Catalytic role of the C-terminal domains of a fungal non-reducing polyketide synthase.
  • Skellam, E., Hurley, D., Davison, J., Lazarus, C., Simpson, T., Cox, R. (2010). Mutation of key residues in the C-methytransferase domain of a fungal highly reducing polyketide synthase.
  • Bailey, A., Cox, R., Harley, K., Lazarus, C., Simpson, T., Skellam, E. (2007). Characterisation of 3-methylorcinaldehyde synthase (MOS) in Acremonium strictum: first observation of a reductive release mechanism during polyketide biosynthesis.
  • Smith, B., Skellam, E., Oxley, S., Graham, A. (2007). Highly selective synthesis of oxabicycloalkanes by indium tribromide mediated cyclization reactions of epoxyalkanes.

Contracts, Grants and Sponsored Research

    Grant - Research

  • Skellam, E.J., Wang, X., "Molecular and structural studies of the first fungal polyketide synthase / non-ribosomal peptide synthetase adenylation domain toward biomolecular probes design," sponsored by UNT BDI, University of North Texas, $10000 Funded. (2022).
  • Skellam, E.J. (Principal), "Investigating the Scope and Mode of Dimerization Reactions Catalyzed by Fungal Flavin-dependent Monooxygenases," sponsored by Welch Foundation, Private, $300000 Funded. (2023 - 2026).
  • Skellam, E., "Greenhouse-based Production of Fungal-Derived Medicines," sponsored by Keck Foundation, Private, $1400000 Funded. (2022 - 2025).
  • Skellam, E.J. (Principal), longo, a. (Co-Principal), "Exploring drug-resistant transporters as a mechanism to identify potent bioactive molecules in potential biocontrol agents," sponsored by BDI, University of North Texas, $30000 Funded. (2023 - 2024).
  • Skellam, E., "Developing a Biomanufacturing Platform for the Site-Selective Functionalization and Structural Diversification of Cytochalasan-Based Carbon Skeletons," sponsored by NSF, Federal, $309778 Funded. (2021 - 2024).
  • Skellam, E.J., "The chemistry and biology of specialized metabolites produced by the endophytic fungi Acremonium zeae (Sarocladium zeae)," sponsored by Bayer AG / Grants4Ag Initiative, Private, $10000 Funded. (2020 - 2021).
  • Cox, R.J., "Understanding and Exploiting Fungal Bisorbicillinoid Biosynthesis," sponsored by German Research Foundation, Federal, $275000 Funded. (2018 - 2021).
  • Skellam, E.J. (Principal), "Developing a Biomanufacturing Platform for the Site-Selective Functionalization and Structural Diversification of Cytochalasan-Based Carbon Skeletons," sponsored by National Science Foundation, FED, Funded. (2021 - 2024).
  • Skellam, E.J. (Principal), "Grants4Ag," sponsored by Bayer AG, IND, Funded. (2021 - 2023).
  • Skellam, E., "The chemistry and biology of specialized metabolites produced by the endophytic fungi Acremonium zeae (Sarocladium zeae)," sponsored by Bayer AG / Grants4Ag Initiative, Private, Funded. (2020 - 2021).
  • Cox, R.J., "Understanding and Exploiting Fungal Bisorbicillinoid Biosynthesis," sponsored by German Research Foundation, Federal, Funded. (2018).
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Overall
Summative Rating
Challenge and
Engagement Index
Response Rate

out of 5

out of 7
%
of
students responded
  • Overall Summative Rating (median):
    This rating represents the combined responses of students to the four global summative items and is presented to provide an overall index of the class’s quality. Overall summative statements include the following (response options include a Likert scale ranging from 5 = Excellent, 3 = Good, and 1= Very poor):
    • The course as a whole was
    • The course content was
    • The instructor’s contribution to the course was
    • The instructor’s effectiveness in teaching the subject matter was
  • Challenge and Engagement Index:
    This rating combines student responses to several SPOT items relating to how academically challenging students found the course to be and how engaged they were. Challenge and Engagement Index items include the following (response options include a Likert scale ranging from 7 = Much higher, 4 = Average, and 1 = Much lower):
    • Do you expect your grade in this course to be
    • The intellectual challenge presented was
    • The amount of effort you put into this course was
    • The amount of effort to succeed in this course was
    • Your involvement in course (doing assignments, attending classes, etc.) was
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