Dept. of Biochemistry & Molecular Biology 208 South Frear Laboratory University Park, PA 16802 Telephone: 814-865-1247 Click here to send email to atp@psu.edu |
As an emeritus faculty member since 2001, I no longer
regularly teach BMB lecture classes but in Spring 2009 I offered a
1-credit course on "Practical Aspects of Enzymology" (BMB 497A) and
likely will teach that course again in 2010. This was the result
of an initiative by Provost Erickson to get emeritus faculty involved
in teaching; in my case, I was allowed to design my own course based on
my belief that most BMB students are in need of additional training in
enzymology, particularly in the use of kinetics for multisubstrate
reactions, as well as how enzymes are being employed in industry and
clinical applications nowadays. The 2009 class was taken by
undergrad and graduate students in BMB, Chemistry, Ag. Engineering and
Food Science, hopefully illustrating that students from many areas feel
the need for more exposure to enzymes and their properties, especially
when approached from a practical standpoint. In teaching this
class, I have had the invaluable assistance of Dr. Lorraine Mulfinger,
Assoc. Prof. of Endocrinology at HMC and also associated with the
Program in Diabetes and Obesity at Hershey and UP campuses; Dr.
Mulfinger brings to the class special expertise in clinical
applications that is of great benefit.
I continue to be very involved in research on
histidine
metabolism and several other projects involving microbial physiology
and
biochemistry. BMB or Microbiology majors who might wish to
get some research experience as part of their undergraduate training
are
encouraged to contact me for information on what my research involves
and
whether there are currently any openings for undergrad researchers in
the
laboratory; this information is also available through the BMB
Department office which coordinates student research interests with
faculty research topics. Below are a few general details
that might be of value to those exploring research opportunities.
In recent years we usually have had one WISER student conducting
research each semester, and I have supervised Honors thesis research
for several Scholars Program students as well as persons simply looking
for research experience. While I do not have assigned advising
duties for BMB undergraduates; if I can be of assistance to
anyone needing academic or professional advising, please feel free to
call on me.
Research focus: Enzymology and molecular
genetics, particularly concerning histidine metabolism
Usual qualifications needed: Some knowledge
of organic chemistry, biochemistry, and general microbiology
Mutational techniques are valuable tools in the analysis of
metabolic
pathways and their regulation, as well as for creating altered forms of
enzymes and for obtaining modified genetic material to permit cloning
for
high level gene expression. Students working in this lab may be
involved
in construction and selection of mutants blocked in specific steps of
histidine
degradation. Characterization of the mutants at the molecular
level
may involve enzyme activity analysis, molecular biological techniques
such
as subcloning into a plasmid vector, electrophoresis of restriction
enzyme
digestion products, and isolation of fragments for DNA sequence
analysis.
Also, site-directed mutations may be created to produce other desired
mutational
changes. These studies may be coupled with efforts to
characterize one or more of the enzymes involved in the histidine
utilization pathway. Currently students are working on urocanase,
a mechanistically unique NAD-dependent hydro-lyase, on the catalytic
properties of formyl-glutamate amidohydrolase, and on the hut repressor
protein which is a DNA-binding protein with unusual sequence
recognition properties. In addition,
isolation
of pathway intermediates, produced either by chemical synthesis or from
blocked mutants, can provide practical experience in the chemical and
biochemical
properties of histidine metabolites. In this area, efforts are
currently focused on the toxic nature of the intermediate imidazolone
propionate (or one of its breakdown products) and by what mechanism
does this material produce its toxicity on cell growth when it is
unable to be metabolized due to absence of the imidazolone propionate
hydrolase.