1982 – 1986 Research Associate,
Biochemical Engineering Laboratory, Department of Chemical Engineering
and Applied Chemistry, Columbia University, New York, USA. Subject:
Production, design and use of microbial lytic enzyme systems. Continuous
culture studies of multienzyme system synthesis and regulation.
Use of enzyme systems in the lysis of yeast and bacteria.
1985 – Ph. D. Biochemical Engineering
, University of London , 1985. Topic: Regulation of Microbial Enzyme
Synthesis Title: The Synthesis and Regulation fo Lytic Enzyme Systems
by Cytophaga sp. and Oerskovia sp.
1979 – 1980 Research Assistant,
Department of Biochemistry, School of Medicine, Universidad of Chile
1977 – BSc. Biochemistry, Queen
Elizabeth College, University of London.
52 publications in international
journals, ISI, with peer review (in English)
Research Interests
Biotechnology and Metabolic Engineering
The group of Professor Dr. B. Andrews
uses metabolic engineering and metabolic flux analysis to optimize
the synthesis of recombinant proteins in yeast cells using as a
model system the synthesis of high levels of intracellular recombinant
protein (human superoxide dismutase, SOD) in S.cerevisiae rhSOD
2060 411 SGA122 cultures, and its comparison with the wild type
strain (without the expression system, not producing the recombinant
protein). These studies allow the analysis and optimization of all
the metabolic fluxes involved in a cell during the synthesis of
a recombinant protein, a stoichiometric model was built, which includes
78 reactions, according to metabolic pathways operative in these
strains. The results suggest conditions that favor the synthesis
and can improve specific production of SOD. The comparison of cells
with and without plasmid using DNA Microarray technology is currently
underway. We are planning to expand this analysis to animal cell
cultures.
Another important area of research
is concerned with the study of protein separation in Aqueous Two-Phase
Systems, this has included studies of phase separation and more
recently how the physico chemical properties, mainly hydrophobicity
and charge, of proteins can be used to predict their partitioning. |