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The long-term
goal of my research program is to improve our understanding of phytoplankton
physiological ecology, population dynamics, community structure,
and ecosystem roles by taking an autecological approach to investigating
the lives of these microorganisms. The tools we use to answer these
questions include observational and experimental (e.g., dilution
gradient and nutrient addition) field studies, which are analyzed
by techniques such as flow cytometry; lab-based investigations of
phytoplankton physiology using various isolates growing in culture;
and a variety of molecular biological, molecular genetic, and biochemical
techniques. For many reasons, the cyanobacteria are the predominant
model system used in my lab.
One part of
my lab is focused on investigating basic cyanobacterial molecular
genetics and physiology. For example, with support from DOE we are
investigating the function of a thioredoxin-like gene, TxlA, which
is found only in cyanobacteria and photosynthetic eukaryotes. Also
with support from DOE and in collaboration with Chip Lawrence and
coworkers at Wadsworth, we are just embarking on a new project that
will take advantage of the availability of several complete cyanobacterial
genome sequences to define the transcription regulation networks
in cyanobacteria.
Another major
focus of work in my lab grew out of my interest in the utilization
of urea as a nitrogen source by marine Synechococcus. As
part of an NSF-funded Biocomplexity project (http://geoweb.princeton.edu/research/biocomplexity/index.html),
we are investigating the biochemically-defined functional group
of microorganisms that can degrade urea, which is one of many potentially
important but poorly understood forms of organic nitrogen present
in aquatic ecosystems. Since most organisms use the well-conserved
enzyme urease to degrade urea, we have designed oligonucleotide
primers that are expected to be universal; that is, they should
enable us to amplify any urease gene. Application of these primers
to samples from Chesapeake Bay has revealed a very high diversity
of urease sequences. Our current efforts are focused on developing
a similar approach to describe the diversity of phytoplankton, and
to adapt both to high-throughput technologies, such as gene array
hybridization.
A third part
of my lab is focused on investigating the comparative ecology of
the small (<2 mm) planktonic picocyanobacteria that are found
in both marine and freshwater ecosystems. We have been using flow
cytometry and molecular techniques to investigate the picocyanobacteria
in Lake George, NY, which we have found to be numerically dominated
by organisms very much like marine Synechococcus. A similar
project, funded by the Hudson River Foundation, is underway in the
Hudson River Estuary, where we are seeking to define the role of
picophytoplankton in the estuarine food web.
Selected Publications
Zani, S., M.T.
Mellon, J.L. Collier, and J.P. Zehr. 2000. Expression of
nifH genes in natural microbial assemblages in Lake George,
NY detected with RT-PCR. Applied and Environmental Microbiology
66: 3119-3124.
Collier,
J.L. 2000. Flow cytometry and the single cell in phycology.
Journal of Phycology 36: 628-644.
Collier,
J.L. and L. Campbell. 1999. Flow cytometry in molecular aquatic
ecology. In: Molecular Ecology of Aquatic Ecosystems. J.P. Zehr,
ed. Kluwer Academic Publishers. Dordrecht, The Netherlands. Hydrobiologia
401:33-53.
Collier,
J.L., B. Brahamsha, and B. Palenik. 1999. The marine cyanobacterium
Synechococcus sp.WH7805 requires urease (urea amidohydrolase,
EC 3.5.1.5) to utilize urea as a nitrogen source: molecular genetic
and biochemical analysis of the enzyme. Microbiology UK 145:447-459.
Collier,
J.L., and A.R. Grossman. 1995. Disruption of a novel thioredoxin-like
protein alters the cyanobacterial photosynthetic apparatus. Journal
of Bacteriology 177:3269-3276.
Apt, K.E., J.L.
Collier, and A.R. Grossman. 1995. The evolution of the phycobiliproteins.
Journal of Molecular Biology 248:79-96.
Collier,
J.L., S.K. Herbert, D.C. Fork, and A.R. Grossman. 1994. Changes
in the cyanobacterial photosynthetic apparatus during acclimation
to macronutrient deprivation. Photosynthesis Research 42:173-183.
Bhalerao, R.P.,
J.L. Collier, P. Gustaffson, and A.R. Grossman. 1994. The
structure of phycobilisomes in mutants of Synechococcus sp.
Strain PCC 7942 devoid of specific linker polypeptides. Photochemistry
and Photobiology 61:298-302.
Collier,
J.L. and A.R. Grossman. 1994. A small polypeptide triggers complete
degradation of light-harvesting phycobiliproteins in nutrient-deprived
cyanobacteria. EMBO (The European Molecular Biology Organization
Journal) 13:1039-1047.
Collier,
J.L. and A.R. Grossman. 1992. Chlorosis induced by nutrient
deprivation in Synechococcus sp. strain PCC 7942: Not all
bleaching is the same. Journal of Bacteriology 174:4718-4726.
Last revised: July
9, 2002
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