Matthew Gacura

 MatthewD. Gacura

Matthew D. Gacura

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May 7, 2018
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Biography

Stark State College - Biology


Resume

  • 2010

    This project involves understanding the role in which multiple community assembly mechanisms impact saprotrophic fungal community structure. Methods involved with this project include TRFLP analysis and Pyrosequencing of the fungal ITS region.

    Matthew

    Gacura

    Kent State University

    Stark State College

    Youngstown State University

    Gannon University

    Erie

    Pennsylvania Area

    I am in charge of instructing both upper division Microbiology and Nursing Microbiology courses. I am also in the process of developing independent research involving the study of environmental microbiology. This research will be focused on the analysis of fungal and bacterial communities in soil samples along with commercial products.

    Assistant Professor

    Gannon University

    Kent

    OH

    This was a management/coordination position of the general microbiology labs at Kent State University that I was selected for. My duties in this position included: designing and organizing college level experiments in microbiology

    preparing Media and other chemicals needed for experiments

    and mentoring graduate student lab instructors. I was also responsible for mediating any conflicts that may have arisen between graduate student instructors and their students.

    Microbiology Lab Coordinator

    Kent State University

    Youngstown

    OH

    I worked on developing methods for the bio-remediation of contaminated river sediment that was collected from the Mahoning River at sites near Youngstown OH. This research focused on the use of edible white rot fungi

    Pleurotus ostreatus (oyster mushrooms) to mineralize polycyclic aromatic hydrocarbons (PAH)

    which are common contaminants in this system.\n\nDuring my time at Youngstown State I instructed for multiple laboratory sections of classes. These classes included: Environmental Microbiology

    Environmental Biotechnology

    General Biology 1

    General Biology 2

    and General Microbiology.

    Graduate Research and Teaching Assistant

    Youngstown State University

    Canton

    Ohio Area

    I have been in charge of lecturing: General Microbiology

    Environmental Science and General Biology 1. I have also instructed the lab components for the previously mentioned classes as well. This position has involved: laboratory management

    lesson plan development

    leadership

    collaboration with other instructors/employees at other institutes

    and management/mentoring of large groups of students. I have taught during both traditional Fall/Spring semesters and during more abbreviated/ faster paced Summer semesters.

    Adjunct Faculty

    Stark State College

    Canton

    Ohio Area

    I was an on call substitute instructor for the general microbiology lecture and lab. This position required being able to instruct students in both the microbiology lecture and lab with very short notice.

    Substitute Instructor

    Stark State College

    Youngstown

    OH

    I was involved in many tasks in this position. My worked focused mainly on the delivery of packages and inventorying equipment throughout the department of biological sciences. I was also involved in routine maintenance on some pieces of equipment and with the cleanup of hazardous chemicals.

    Laboratory Clerk

    Youngstown State University

    Kent

    OH

    I worked on projects dealing with the assembly of saprotrophic microbial communities

    and investigating functional redundancy. This research was focused on processes including: environmental factors

    dispersal limitation

    and priority effects. At the same time I developed methods and tools for characterizing the aggregated functional traits found in these communities

    to allow for a better understanding about functional redundancy in these complex systems. During this time I have also had extensive training in next generation sequencing and analysis of meta-genomic data sets. \n\nI have also instructed General Microbiology lab and General Ecology lab for multiple semesters. This has allowed me to have extensive training in lecturing

    development of teaching materials and interacting with/mentoring undergraduates.

    Graduate Research and Teaching Assistant

    Kent State University

    Member

    Ecological Society of America

    American Society of Microbiology

    Biology Graduate Student Council

    Vice President and President

    English

    Herrick Aquatic Ecology Research Grant

    An annual research grant awarded by the biology department for two thousand dollars.

    Kent State University Department of Biological Sciences

    Outstanding Lab Coordinator Award

    This award is given in recognition of outstanding work as a lab coordinator during an academic year. This award was received in recognition of my success as the general microbiology lab coordinator.

    Kent State University Department of Biological Sciences

  • 2009

    Doctor of Philosophy (PhD)

    My PhD is in soil biology

    microbial ecology and ecology. The focus of my dissertation research is on the mechanisms responsible for the assembly of saprotrophic fungal communities and how community composition relates to community aggregated functional traits. I have taken many classes in microbiology

    microbial ecology

    biology statistics

    environmental science

    soil biology

    and ecology. I defended my dissertation in October of 2018 and graduated in December.

    Ecology

    Soil Biology

    and Environmental Microbiology

    Graduate Student Council Vice President (2011-2012) and Graduate Student President (2012-2014)

    Kent State University

  • 2007

    This project involved the use of Pleurotus ostratus (oyster mushrooms) to break down persistent chemicals found in Mahoning River sediment.

    Master of Science (MS)

    I received my masters of science in biological sciences. During this time I was involved in thesis research dealing with bioremediation of contaminated river sediment.

    Biology

    General

    I joined the American Society of Microbiology

    Youngstown State University

  • 2003

    I was in charge of judging several presentations on student projects from Stark State College.

    Stark State College

    Volunteer microbiology lab guide for prospective freshman

    Kent State University

    Volunteer Science Lecturer

    I volunteered as a biotechnology lecturer for 7 class periods. I was able to instruct students on the uses of microorganisms in biotechnology. During this time I was also able to field questions on applying to college and how to eventually get into graduate school.

    Poland Seminary High School

    Volunteer Staff

    I helped supervise volunteers who were planting trees

    in the set up of long term experimental forest plots in Cuyahoga Valley National Park. Volunteers under my supervision included college

    high school and middle school students.

    Kent State University

    Microbiology Judge

    Judged middle and high school student science fair projects.

    NEOSTEM middle school and high school science fair

    DNA extraction

    Molecular Biology

    Mycology

    Western Blotting

    Scientific Writing

    Microbiology

    Student Development

    Biology

    Student Affairs

    Research

    Science

    Fluorescence Microscopy

    Ecology

    Confocal Microscopy

    Laboratory

    Gel Electrophoresis

    Teaching

    PCR

    Cell Culture

    Higher Education

    Effect of Pleurotus ostreatus on Bioremediation of PAH Contaminated River Sediment.

    The purpose of this study was to optimize bioremediation of Mahoning River sediment historically contaminated with polycyclic aromatic hydrocarbons (PAHs) using white rot fungi. Pleurotus ostreatus grown on grain (10% v/v) was added to contaminated sediment amended with sawdust (80% v/v)

    with and without fungal specific nutritional nitrogen (to enhance fungal growth)

    and with cyclodextrin (to increase PAH availability). Sediment mixtures were incubated in the dark at 25°C for 6 weeks. Fungal biomass

    determined using fluorescent microscopy

    indicated initial fungal colonization but then fungal growth was inhibited

    likely by toxic metals or high moisture content in the sediment. Growth of unidentified fungi was observed

    especially in treatments amended with nitrogen. Total PAH concentrations (in the order of 100 ppm)

    analyzed using a gas chromatograph mass spectrometer (GCMS)

    and significantly decreased ~ 50-60% in all treatments

    including sediment only controls within the first two weeks. Thus

    aerobic degradation by native bacteria and volatilization were likely responsible for most of the observed decreases in PAH concentrations. High heterogeneity of PAHs in this historically contaminated sediment led to high variance between replicates. There was a slight decrease in 5 ring PAHs associated with sediment inoculated with P. ostreatus and also a slight decrease in total PAH concentrations associated with sediment amended with sawdust and cyclodextrin (with or without P. ostreatus). Increased nitrogen did not enhance PAH degradation. Sediment inoculated with P. ostreatus after two weeks

    rather than initially

    showed better fungal growth and colonization

    but PAH data was not yet available. These data indicate there is great potential for bioremediation of PAH contaminated sediment conditions by stimulating indigenous bacteria under aerobic conditions followed by the addition of white rot fungi.

    Effect of Pleurotus ostreatus on Bioremediation of PAH Contaminated River Sediment.

    Bess Heidenreich

    Fungi have developed a wide assortment of enzymes to break down pectin

    a prevalent polymer in plant cell walls that is important in plant defense and structure. One enzyme family used to degrade pectin is the glycosyl hydrolase family 28 (GH28). In this study we developed primers for the amplification of GH28 coding genes from a database of 293 GH28 sequences from 40 fungal genomes. The primers were used to successfully amplify GH28 pectinases from all Ascomycota cultures tested

    but only three out of seven Basidiomycota cultures. In addition

    we further tested the primers in PCRs on metagenomic DNA extracted from senesced tree leaves from different forest ecosystems

    followed by cloning and sequencing. Taxonomic specificity for Ascomycota GH28 genes was tested by comparing GH28 composition in leaves to internal transcribed spacer (ITS) amplicon composition using pyrosequencing. All sequences obtained from GH28 primers were classified as Ascomycota; in contrast

    ITS sequences indicated that fungal communities were up to 39% Basidiomycetes. Analysis of leaf samples indicated that both forest stand and ecosystem type were important in structuring fungal communities. However

    site played the prominent role in explaining GH28 composition

    whereas ecosystem type was more important for ITS composition

    indicating possible genetic drift between populations of fungi. Overall

    these primers will have utility in understanding relationships between fungal community composition and ecosystem processes

    as well as detection of potentially pathogenic Ascomycetes.

    Comparison of pectin-degrading fungal communities in temperate forests using glycosyl hydrolase family 28 pectinase primers targeting Ascomycete fungi

    Saprotrophic fungal communities are highly complex ecological units responsible for a wide range of terrestrial ecosystem functions

    most notably the decomposition/recycling of large amounts of senesced plant tissue. These communities may be assembled by several distinct community assembly mechanisms that could be categorized into two broad groups: deterministic processes based around environmental selection

    and more stochastic mechanisms arising from dispersal limitation and colonization history. However

    there is much conjecture about which mechanism plays the most critical role in the formation of these ecological units. Furthermore

    the spatial scale of inquiry may also influence the relative importance of these mechanisms in determining community composition. This dissertation was focused on determining the relative importance of multiple community assembly mechanisms on community composition of saprotrophic fungal communities at both large and small scales. In addition

    the importance of these mechanisms in the distribution of community aggregated functional traits was also investigated.\nAn observational approach based on a detailed sampling scheme of senesced leaves allowed for investigating the importance of how spatial scale impacts the relative importance of community assembly mechanisms. The importance of community assembly history

    also known as priority effects

    was analyzed using a manipulative experimental approach that involved the modification of the starting communities of saprotrophic fungi and its impact on later colonization. Community composition was analyzed using both terminal restriction fragment length polymorphism (TRFLP) and next generation sequencing technology (pyrosequencing). Community aggregated functional traits were analyzed through the identification of fungal functional groups of OTUs

    analysis of GH28 pectinase genes

    and the quantification of extracellular enzyme activity. \n

    Drivers of Fungal Community Composition and Function in Temperate Forests

    This project involves understanding the role in which priority effects impact microbial community composition

    community aggregated functional traits

    and related ecosystem processes. Methods involved in this project include TRFLP analysis and quantification of extracellular enzymes.

    Fungal specific GH28 pectinase primers.

    This project involved the development of fungal specific GH28 pectinase gene primers for the analysis of environmental samples. Methods involved in this project included: Clone Libraries

    Sanger Sequencing

    and Pyrosequencing of the Fungal ITS region. This project was finished and published in the Journal of Microbiology Methods in 2016.

    Bachelor of Science (B.S.)

    I performed research in a environmental microbiology lab as a undergraduate and graduate student. The research focused on amplifying American Elm tree DNA for conservation purposes and the use of fungi for bioremediation of contaminated river sediment.

    Biology

    General

    American Society of Microbiology\n

    Youngstown State University

    Ecology of Forest Fungi

    Soil Biology

    Biological Statistics

    Advanced Microbiology

    Advanced Community Ecology