Problem Solver

Eric Becker

Areas Eric Becker is Knowledgeable in:

Microbiology
Molecular Biology
Bacteriology
Bacterial Genetics
Plasmid Biology
Fluorescent Microscopy
Bio-chamber design
Bio-reactor design
Environmental Simulation

Techniques Eric Becker Uses:

Iterations of brainstorming sessions and pilot experiments to narrow the choice of potential solutions. Brainstorming consists of web based research and discussions with colleagues. Evaluation of prototypes generally leads to refinement and ultimately a working product.

Eric Becker's Problem Solving Skills:

  1. Bioreactor automation
  2. PLC programing
  3. Directed evolution
  4. Algal transformation
  5. Algal genetics
  6. Mutagenesis
  7. Timelapse microscopy
  8. Micro-biochamber design
  9. Protoplast fusion
  10. TIRF microscopy
  11. Bacterial conjugation
  12. Plasmid biology
  13. Fluorescent microscopy
  14. Microbial genetics
  15. Turbidostat/chemostat design
  16. Algal bioreactor design
  17. Environmental simulation (temperature, pH, light)
  18. Bio-energy (algal strain optomization for bio-energy production)
  19. GFP tagging
  20. Phage display
  21. Fluorescent labeling of membranes, proteins, and DNA

Eric Becker's Problem Solving Experience:

  1. Molecular Memory: Constructed B. subtilis strains with "molecular memory" to determine if plasmids segregate to the forespore post-septation during sporulation. This system relied on cell-specific gene expression of DNA recombinases and gene activation by DNA recombination.
  2. HTP 96w Growth Assay: Developed a HTP clone-screening platform that provides uniform light, temperature, culture mixing, CO2 and culture evaporation.
  3. Cell-specific GFP Tagging: Developed in vivo GFP tagging methods to determine the asymmetric distribution of membrane proteins positioned between cells
  4. Time-lapse Microscopy: Developed methods to enable efficient time-lapse analysis of membranes, DNA, and fluorescently labeled proteins during sporulation and growth in B. subtilis
  5. Gene Fusion and Deletion: Formulated cloning vectors that utilize site specific recombination to create non-polar in-frame gene deletions.
  6. Algal bio-reactors: Developed and constructed bio-reactors for evaluation of algal strains capable of maintaining constant pH, Optical Density, temperature, irradiance and turbulence for an algal bio-fuel company
  7. Environmental simulator: Developed automated algal growth systems that simulate fluctuating environmental conditions of outdoor production ponds in the lab.
  8. Phage Display: Constructed a series of phagemid vectors that allow efficient display of randomly fragmented gene sequences
  9. UCSD Provisional Patent: Developed a transposon for random insertion of GFP into target proteins, while maintaining normal transcriptional and translational control