Karen Klyczek
University of Wisconsin–River Falls
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Publication
Featured researches published by Karen Klyczek.
Nature microbiology | 2017
Rebekah M. Dedrick; Deborah Jacobs-Sera; Carlos Bustamante; Rebecca A. Garlena; Travis N. Mavrich; Welkin H. Pope; Juan C. Cervantes Reyes; Daniel A. Russell; Tamarah L. Adair; Richard Alvey; J. Alfred Bonilla; Jerald S. Bricker; Bryony R. Brown; Deanna Byrnes; Steven G. Cresawn; William B. Davis; Leon A. Dickson; Nicholas P. Edgington; Ann M. Findley; Urszula Golebiewska; Julianne H. Grose; Cory F. Hayes; Lee E. Hughes; Keith W. Hutchison; Sharon Isern; Allison Johnson; Margaret A. Kenna; Karen Klyczek; Catherine M. Mageeney; Scott F. Michael
Temperate phages are common, and prophages are abundant residents of sequenced bacterial genomes. Mycobacteriophages are viruses that infect mycobacterial hosts including Mycobacterium tuberculosis and Mycobacterium smegmatis, encompass substantial genetic diversity and are commonly temperate. Characterization of ten Cluster N temperate mycobacteriophages revealed at least five distinct prophage-expressed viral defence systems that interfere with the infection of lytic and temperate phages that are either closely related (homotypic defence) or unrelated (heterotypic defence) to the prophage. Target specificity is unpredictable, ranging from a single target phage to one-third of those tested. The defence systems include a single-subunit restriction system, a heterotypic exclusion system and a predicted (p)ppGpp synthetase, which blocks lytic phage growth, promotes bacterial survival and enables efficient lysogeny. The predicted (p)ppGpp synthetase coded by the Phrann prophage defends against phage Tweety infection, but Tweety codes for a tetrapeptide repeat protein, gp54, which acts as a highly effective counter-defence system. Prophage-mediated viral defence offers an efficient mechanism for bacterial success in host–virus dynamics, and counter-defence promotes phage co-evolution.
American Biology Teacher | 2006
Mark Bergland; Mary Lundeberg; Karen Klyczek; Jennifer Sweet; Jean Emmons; Christine Martin; Katherine Marsh; Joy Werner; Michelle Jarvis-Uetz
oday, teachers face more challenges than ever, and biology teachers face a special challenge. As technology continues to expand, biology teachers have a responsibility to keep students informed of technological and scientific advances. Biology teachers must also address ethical issues associated with these advances. Here we describe our experiences using case-based molecular biology simulations in high school and introductory college biology classes. This software enables teachers to meet several national science standards, such as connecting science to real-life situations and encouraging students to think about the relationships among science, technology and society. The realistic simulation also encourages students to explore careers in molecular biology and genetics, and gives students experience both in building Web pages and Internet conferencing.
PLOS ONE | 2015
Steven G. Cresawn; Welkin H. Pope; Deborah Jacobs-Sera; Charles A. Bowman; Daniel A. Russell; Rebekah M. Dedrick; Tamarah L. Adair; Kirk R. Anders; Sarah Ball; David Bollivar; Caroline A. Breitenberger; Sandra H. Burnett; Kristen Butela; Deanna Byrnes; Sarah Carzo; Kathleen Cornely; Trevor Cross; Richard L. Daniels; David Dunbar; Ann M. Findley; Chris R. Gissendanner; Urszula Golebiewska; Grant A. Hartzog; J. Robert Hatherill; Lee E. Hughes; Chernoh S. Jalloh; Carla De Los Santos; Kevin Ekanem; Sphindile L. Khambule; Rodney A. King
Mycobacteriophages – viruses of mycobacterial hosts – are genetically diverse but morphologically are all classified in the Caudovirales with double-stranded DNA and tails. We describe here a group of five closely related mycobacteriophages – Corndog, Catdawg, Dylan, Firecracker, and YungJamal – designated as Cluster O with long flexible tails but with unusual prolate capsids. Proteomic analysis of phage Corndog particles, Catdawg particles, and Corndog-infected cells confirms expression of half of the predicted gene products and indicates a non-canonical mechanism for translation of the Corndog tape measure protein. Bioinformatic analysis identifies 8–9 strongly predicted SigA promoters and all five Cluster O genomes contain more than 30 copies of a 17 bp repeat sequence with dyad symmetry located throughout the genomes. Comparison of the Cluster O phages provides insights into phage genome evolution including the processes of gene flux by horizontal genetic exchange.
international conference on human interface and management of information | 2011
Chi-Cheng Lin; Mark Bergland; Karen Klyczek
Biology students need exposure to modern research techniques relatively early in their educational careers. Computer multimedia simulation tools have been developed to address the challenge of providing all students with hands-on laboratory research experience. This paper presents a learner-centered approach to the design and development of a multimedia simulation for biology education. We present our methodology and a multimedia simulation tool designed and developed using the methodology. Out tool has been widely adopted by biological science educators for teaching molecular biology subjects in a wide range of undergraduate biology courses. We believe that our methodology can be adopted or adapted by learner communities in other disciplines.
Genome Announcements | 2017
Welkin H. Pope; Matthew T. Montgomery; J. Alfred Bonilla; Randall J. DeJong; Rebecca A. Garlena; Carlos Bustamante; Karen Klyczek; Daniel A. Russell; John T. Wertz; Deborah Jacobs-Sera; Graham F. Hatfull
ABSTRACT We report here the genome sequences of 38 newly isolated bacteriophages using Gordonia terrae 3612 (ATCC 25594) and Gordonia neofelifaecis NRRL59395 as bacterial hosts. All of the phages are double-stranded DNA (dsDNA) tail phages with siphoviral morphologies, with genome sizes ranging from 17,118 bp to 93,843 bp and spanning considerable nucleotide sequence diversity.
Science | 2012
Mark Bergland; Karen Klyczek; Chi-Cheng Lin; Mary Lundeberg; Rafael Tosado-Acevedo; Arlin Toro; Dinitra White; Bjørn H. K. Wolter
Case It!, an IBI prize–winning module, provides computer simulations that enable student analysis of biological materials not usually available in laboratories. Case It! (www.caseitproject.org) originated at the 1995 BioQUEST Summer Workshop (1) and has developed over the years into an effective system for case-based learning useful for both high school and university educators (2, 3). National Science Foundation support has enabled us to distribute all project materials at no cost.
Genome Announcements | 2018
Karen Klyczek; Deborah Jacobs-Sera; Tamarah L. Adair; Sandra D. Adams; Sarah Ball; Robert C. Benjamin; J. Alfred Bonilla; Caroline A. Breitenberger; Charles J. Daniels; Bobby L. Gaffney; Melinda Harrison; Lee E. Hughes; Rodney A. King; Gregory P. Krukonis; A. Javier Lopez; Kirsten Monsen-Collar; Marie C. Pizzorno; Claire A. Rinehart; Amanda K. Staples; Emily Stowe; Rebecca A. Garlena; Daniel A. Russell; Steven G. Cresawn; Welkin H. Pope; Graham F. Hatfull
ABSTRACT We report here the complete genome sequences of 44 phages infecting Arthrobacter sp. strain ATCC 21022. These phages have double-stranded DNA genomes with sizes ranging from 15,680 to 70,707 bp and G+C contents from 45.1% to 68.5%. All three tail types (belonging to the families Siphoviridae, Myoviridae, and Podoviridae) are represented.
Journal of Microbiology & Biology Education | 2016
Jack A. Gilbert; Karen Klyczek; Samantha L. Elliott
In this Editorial, the three Guest Editors for JMBEs first standalone themed issue introduce the topic of scientific citizenship and provide an overview of the current ideas and best practices contained within the issue.
Cellular Immunology | 1992
Louis A. Rosenthal; Karen Klyczek; Kenneth J. Blank
Kgv cells do not constitutively express class I mRNA or protein. Interferon (IFN)-gamma, but not IFN-alpha/beta, induces H-2Dk expression. IFN does not induce H-2Kk expression. We examined constitutive and IFN-inducible class I expression on Kgv cells stably transfected with genomic clones of H-2Kk or H-2Dk and on somatic cell hybrid lines constructed between Kgv cells and constitutively class I-positive cells of a distinguishable H-2 haplotype. Our results suggest that both the lack of constitutive class I expression and the inability of IFN-alpha/beta to induce class I expression on Kgv cells are primarily due to cis-regulatory mechanisms. However, stable introduction of the H-2Dk gene into Kgv cells conferred IFN-gamma inducibility upon the silent endogenous H-2Kk gene. Therefore, the failure of IFN-gamma to induce H-2Kk expression on Kgv cells is due, at least in part, to a trans-regulatory mechanism.
The Journal of Experimental Biology | 2015
Renata S. Borba; Karen Klyczek; Kim Mogen; Marla Spivak