Anne Schwarzkopf (Alexander), Ph.D. profile photo

Anne Schwarzkopf (Alexander), Ph.D.

Associate Professor

  • Milwaukee WI UNITED STATES
  • Civil and Architectural Engineering and Construction Management

Dr. Schwarzkopf teaches chemistry, biochemistry, environmental chemistry, cell biology & genetics, microbiology, & prokaryotic processes.

Education, Licensure and Certification

Ph.D.

Environmental Engineering

University of Iowa

2010

B.S.

Environmental Science

University of Iowa

2004

Biography

Dr. Anne Schwarzkopf teaches chemistry, biochemistry, environmental chemistry, cell biology and genetics, microbiology, and prokaryotic processes courses in the Physics and Chemistry Department at Milwaukee School of Engineering. Her graduate and postdoctoral research focused on the molecular mechanisms of bioremediation, biocatalysis, and plant/nanoparticle interactions.

Areas of Expertise

Chemistry
Environmental Engineering
Bioremediation
Biocatalysis
Microbiology

Accomplishments

Oscar Werwath Distinguished Teacher Award

2019-2020
The award was established by the university in 1967 to recognize excellence in teaching. All nominees for this award must have a minimum of seven years of full-time service to MSOE. Students choose the award winner through two rounds of voting.

Center for Biocatalysis and Bioprocessing Graduate Fellowship

2009-2010

National Science Foundation Graduate Research Fellowship

2006-2009

Social

Event and Speaking Appearances

Interactions of Plants and Engineered Nanoparticles

International Phytotechnology Conference  Portland, OR, September 2011

Nanoparticle-Plant Interactions: Transport and Toxicity

Marquette University  Milwaukee, WI, November 2012

Endless Possibilities: Collaborations with MSOE to Facilitate Student Learning with 3D Physical and Virtual Models

Biennial Conference on Chemical Education  University of Notre Dame, July 2018

Selected Publications

The genome of Polaromonas sp. strain JS666: insights into the evolution of a hydrocarbon-and xenobiotic-degrading bacterium, and features of relevance to biotechnology

Applied and Environmental Microbiology

Mattes, T.E., Alexander, A.K., Richardson, P.M., Munk, A.C., Han, C.S., Stothard, P., Coleman, N.V.

2008

Polaromonas sp. strain JS666 can grow on cis-1,2-dichloroethene (cDCE) as a sole carbon and energy source and may be useful for bioremediation of chlorinated solvent-contaminated sites. Analysis of the genome sequence of JS666 (5.9 Mb) shows a bacterium well adapted to pollution that carries many genes likely to be involved in hydrocarbon and xenobiotic catabolism and metal resistance. Clusters of genes coding for haloalkane, haloalkanoate, n-alkane, alicyclic acid, cyclic alcohol, and aromatic catabolism were analyzed in detail, and growth on acetate, catechol, chloroacetate, cyclohexane carboxylate, cyclohexanol, ferulate, heptane, 3-hydroxybenzoate, hydroxyquinol, gentisate, octane, protocatechuate, and salicylate was confirmed experimentally. Strain JS666 also harbors diverse putative mobile genetic elements, including retrons, inteins, a miniature inverted-repeat transposable element, insertion sequence transposases from 14 families, eight genomic islands, a Mu family bacteriophage, and two large (338- and 360-kb) plasmids. Both plasmids are likely to be self-transferable and carry genes for alkane, alcohol, aromatic, and haloacid metabolism. Overall, the JS666 genome sequence provides insights into the evolution of pollutant-degrading bacteria and provides a toolbox of catabolic genes with utility for biotechnology.

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Bioremediation and biocatalysis with Polaromonas sstrain JS666

University of Iowa - Dissertation

Alexander, A.

2010

Polaromonas sp. strain JS666 is the only isolated bacterium capable of aerobic growth using the groundwater pollutant cis-1,2-dichloroethene (cDCE) as a sole carbon source. Its genome has a wealth of evidence of recent gene acquisition through horizontal gene transfer, and contains gene clusters predicted to encode enzymes allowing the metabolism of a wide variety of xenobiotic compounds. Culture growth using each of these hypothesized substrates was tested experimentally, and many were confirmed as sole carbon sources for strain JS666. In addition to pollutant degradation, many of these metabolic pathways have applicability in the field of biocatalysis, as does the genome-assisted pathway prediction approach to biocatalyst discovery.

During (or immediately following) growth on cDCE, cultures of Polaromonas sp. strain JS666 oxidize ethene to epoxyethane at an increased rate, and also cometabolically oxidize several other chlorinated ethenes. Given the involvement of a monooxygenase in other species' 1-chloroethene (vinyl chloride) oxidation, it was hypothesized that alkene oxidation in strain JS666 was due to the activity of a monooxygenase that also was responsible for the first step in cDCE oxidation. The alkene oxidation activity of strain JS666 was investigated using gene expression analysis, proteomics, and whole-cell kinetic assays. Results of these experiments pointed to the upregulation of a cyclohexanone monooxygenase (CHMO) during growth on cDCE and during oxidation of ethene.

To determine the activity of this cyclohexanone monooxygenase, its gene was cloned and heterologously expressed in an E. coli host. Our CHMO expression system exhibited activity on cyclohexanone, but not cDCE or ethene, disproving our hypothesis about its involvement in alkene oxidation. The heterologously expressed monooxygenase was also investigated for enantioselective oxidation of racemic cyclic ketones to chiral lactones, and was discovered to have very high enantioselectivity with the tested compounds. Chiral lactones and other single-enantiomer oxidation products are valuable for fine chemical synthesis, and their biocatalytic production is more environmentally sustainable and often less expensive than traditional techniques.

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Aerobic biodegradation of the chloroethenes: pathways, enzymes, ecology, and evolution

FEMS Microbiology Reviews

Mattes, T.E., Alexander, A.K., Coleman, N.V.

2010

Extensive use and inadequate disposal of chloroethenes have led to prevalent groundwater contamination worldwide. The occurrence of the lesser chlorinated ethenes [i.e. vinyl chloride (VC) and cis-1,2-dichloroethene (cDCE)] in groundwater is primarily a consequence of incomplete anaerobic reductive dechlorination of the more highly chlorinated ethenes (tetrachloroethene and trichloroethene). VC and cDCE are toxic and VC is a known human carcinogen. Therefore, their presence in groundwater is undesirable. In situ cleanup of VC- and cDCE-contaminated groundwater via oxidation by aerobic microorganisms is an attractive and potentially cost-effective alternative to physical and chemical approaches. Of particular interest are aerobic bacteria that use VC or cDCE as growth substrates (known as the VC- and cDCE-assimilating bacteria). Bacteria that grow on VC are readily isolated from contaminated and uncontaminated environments, suggesting that they are widespread and influential in aerobic natural attenuation of VC. In contrast, only one cDCE-assimilating strain has been isolated, suggesting that their environmental occurrence is rare. In this review, we will summarize the current knowledge of the physiology, biodegradation pathways, genetics, ecology, and evolution of VC- and cDCE-assimilating bacteria. Techniques (e.g. PCR, proteomics, and compound-specific isotope analysis) that aim to determine the presence, numbers, and activity of these bacteria in the environment will also be discussed.

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