Fungi class

The Microbiology Area is especially strong in teaching students superior lab technique. Classes involve many hours perfecting skills in the lab, and address a wide variety of microbiological topics, including ones of medical interest, ecological relevance, and prokaryotic diversity.

Larry Baresi - methane-producing bacteria

Larry BaresiProfessor
D.P.H. University of California, Los Angeles
Phone: 818-677-3495
Fax: 818-677-2034 
Office: Magnolia Hall 4201

I have three major research interests. The first is the exploration of methane producing bacteria as a unified physiological, biochemical, and genetic model system. I am also interested in isolation and identification of extremophiles for evolutionary purposes.  Finally, I work on the identification and isolation of environmentally important bacteria involved in the remediation of toxic wastes. These three groups of bacteria survive and grow in unusually "extreme" environmental habitats. Such habitats may place constraints of pH, salt, or temperature on the physiology of these organisms, forcing them to develop unique molecular solutions, which may be harnessed for technological applications. I'm currently developing a genetic vector capable of transferring DNA between methanogens and other bacteria. This work includes techniques of genetic transformation, gene manipulation, gene cloning, DNA isolation and purification, and other molecular genetic techniques. My primary effort on extremophiles is the isolation, identification, enzymology, and physiology of these unique organisms. Such studies will suggest how these organisms evolved, and how these organisms might be applied to existing or new industrial processes and the problems of toxic waste remediation.

David Bermudes - live bacteria as therapeutic delivery vectors

David BermudesAssociate Professor
Ph.D. Boston University
Phone: 818-677-6062
Fax: 818-677-2034
Office: Magnolia Hall 4216

Certain pathogenic bacteria such as Salmonella typhimurium have the innate ability to target and selectively replicate within solid tumors in a number of different animal species, including humans. Pathogenic bacteria can be genetically modified in order to eliminate debilitating aspects of their pathogenesis while retaining their ability to traverse the body and target tumors.  My laboratory is exploring a variety of mutations in Salmonella that decrease pathogenesis and/or increase their ability to colonize solid tumors in order to identify strains that have the potential to serve as anticancer agents in humans. In these studies, and in attempts to understand the fundamental nature of the bacterial physiology relating to tumor-targeting, we have identified spontaneous and genetically engineered mutations that have compensatory functions relating to their ability to exist under mammalian physiological conditions and may have the ability to enhance their antitumor effects.

Gilberto Flores - microbial ecology

Gilberto FloresAssistant Professor
Ph.D. Portland State University
Phone: 818-677-4276
Fax: 818-677-2034
Office: Eucalyptus Hall 2208

I am an interdisciplinary scientist who specializes in microbial ecology, exploring the diversity and function of microbial communities in a wide range of environments. I use a combination of cutting-edge molecular biology/bioinformatics tools (such as high-throughput sequencing and genomics) and more traditional microbiological techniques (e.g. cultivation, fluorescent microscopy) to address fundamental questions about the ecology and evolution of microorganisms. I have worked in a wide array of environments including deep-sea hydrothermal vents, terrestrial hot-springs, public restrooms and the human body. Currently, I am leading a project examining the temporal variability of the healthy human microbiome using undergraduate students as the study population. Other research interests include microbial oceanography, the pan-genome, geomicrobiology, systems biology, bioremediation and archaeal ecology.

Rachel Mackelprang - environmental metagenomics

Rachel MackelprangAssociate Professor
Ph.D. University of Washington
Phone: 818-677-4589
Fax: 818-677-2034
Office: Eucalyptus Hall 2207

I am a genomicist focused on environmental metagenomics. Microbes are the engines that power fundamental biogeochemical cycles. Large-scale anthropogenic alterations in the environment are predicted to greatly affect microbial life, altering the balance of these cycles in the biosphere. While most microbes in the environment are recalcitrant to culturing, metagenomics provides access to the genomes of "inaccessible" organisms by isolating and sequencing all DNA from a particular environment. I am interested in leveraging ultra high-throughput sequencing, bioinformatic analysis, and microbiology-based approaches to study microbial community response to human-caused environmental perturbations and determine the impact of microbes on biogeochemical cycles. Current study systems include the thawing permafrost, the Gulf of Mexico Deepwater Horizon oil spill, and the great prairie of the Midwestern United States.

Sean Murray - bacterial cell cycle

Sean MurrayProfessor
Ph.D. Yale University, 2003
Phone: 818-677-2950
Fax: 818-677-2034
Office: Eucalyptus Hall 2205

The dimorphic bacterium Caulobacter crescentus is a model organism for studying the bacterial cell cycle. Its asymmetric cell division results in one swarmer and one stalked cell progeny. Motile swarmer cells can not undergo DNA replication until they differentiate into stationary stalked cells. If sufficient nutrients are available, swarmer cells eject their polar flagellum and build a stalk (with adhesive at its end; for attaching to a surface near nutrients) at the same pole formerly occupied by the flagellum. Stalked cells are competent for DNA replication and cell division. During cell division, a flagellum is placed at the pole opposite that of the stalk. Caulobacter's obligate cell cycle is controlled by oscillating master regulators that control different genetic modules in space and time. As a result of this carefully orchestrated process, a flagellum is synthesized only when needed (just prior to cell division) and is placed at the pole opposite that of the stalk. Likewise, a new stalk is synthesized only at the pole previously occupied by a flagellum. Our lab studies the roles of lipid biosynthesis in this process, using pharmacological, genetic, and molecular approaches. Only by further elucidating the control mechanisms of bacterial cell division can we advance the development of new antimicrobial compounds. Lipid biosynthesis is essential for cell viability and bacterial fatty acid synthetic enzymes have been suggested as antibiotic targets. In fact, compounds specific to bacterial fatty acid biosynthetic compounds have been generated. Most previous studies on bacterial lipid metabolism have focused on E. coli, a gamma-proteobacteria. Caulobacter in contrast, as an alpha-proteobacteria, is closely related to human pathogenic bacteria, such as Brucella and Rickettsia.

Cristian Ruiz Rueda - Antibiotic resistance mechanisms in bacteria

Cristian Ruiz RuedaAssistant Professor
Ph.D. University of Barcelona
Phone: 818-677-6217
Fax: 818-677-2034
Office: Eucalyptus Hall 2226D

My ultimate goal is to develop novel ways of preventing and treating infectious diseases caused by bacteria resistant to multiple antibiotics. These bacteria have become a major problem in the U.S. and abroad, from failed treatment of previously curable diseases to increased hospital costs. There are approximately 2 million hospital-acquired infections in the U.S. each year, with more than 99,000 deaths occurring mostly due to antibiotic resistant pathogens. The annual hospital economic cost of resistance is estimated to be greater than $20 billion in the U.S., with additional costs to society for lost productivity as high as $35 billion a year. World health leaders have described antibiotic resistant pathogens as "nightmare bacteria that pose a catastrophic threat to people in every country in the world". My laboratory uses a multidisciplinary approach that includes bacterial genetics and biochemistry, molecular biology, gene expression, and "omics" to: (1) Study the molecular mechanisms of multi-drug resistance, its regulation, and its interconnection with cell metabolism and physiology in order to identify new antimicrobials and targets; and (2) Develop novel molecular detection methods to detect and prevent outbreaks of antibiotic resistant pathogens.

Michael Summers - genetics of cyanobacterial metabolism and differentiation

Michael SummersProfessor
Ph.D. University of California, Davis
Phone: 818-677-7146
Fax: 818-677-2034
Office: Eucalyptus Hall 2213

My laboratory focuses on the problem of how bacteria regulate adaptive alterations of their cell morphology and physiology in response to environmental changes. I use Nostoc punctiforme for these studies. This filamentous cyanobacterium can differentiate from normal vegetative cells into nitrogen fixing heterocysts, resistant akinetes, or motile hormogonia, that move by gliding motility. Our research focuses on identification of genes involved in cellular differentiation of akinetes. Akinetes are resting cells capable of surviving long periods of desiccation and cold that differentiate from normal vegetative cells due to low light or phosphate starvation.