|
|
Steven W. Hutcheson
Professor
Ph.D. - University of California, Berkeley, 1982
Telephone: (301) 405-5498
Fax: (301) 314-9489
E-mail:
hutcheso@umd.edu
Research Interests: Genetics of microbial pathogenesis; role and regulation of type III protein secretion systems; microbial genomics.
RESEARCH OF THE
HUTCHESON LAB
Lignocellulosic
biomass is mostly composed of carbohydrate polymers that can be
degraded to their constituent sugars if cost effective means can be
developed. These sugars or sugar derivatives can then be turned
into various fuels and other specialty chemicals through
fermentation. The limitations in current pretreatments and enzymes
necessitate a search for new methods to release these sugars.
The saprophytic
marine bacterium Saccharophagus degradans is capable of
enzymatically releasing sugars from many complex polysaccharides
using unique mechanisms. This bacterium is from the Chesapeake Bay
and has multiple unusual carbohydrase systems and the accompanying
genetic systems. Thus this bacterium is a repository for unique
enzymes and mechanisms for processing complex polysaccharides. We
are studying the novelties of several of the carbohydrase systems
produced by this bacterium that are most applicable to biofuel
production to provide new tools and techniques.
The approach is to
use modern molecular genetics to answer: how does this bacterium
eat? This is not a simple question as this bacterium eats by
dissolving complex polysaccharides while in an infinitely large
dilutant called the ocean. Thus it must have mechanisms to vector
carbon back to itself. To help us in this quest, the bacterium has
a known genome sequence with a tentative annotation for the genes
and their products. We are using molecular cloning and directed
expression to understand the biochemical function of many of the
gene products. The transcriptome has been analyzed using deep
sequencing (sequencing of the mRNA present in the cell) so that
relative expression of a gene under specific growth conditions can
be estimated and regulatory information in promoters deduced. We
have also used quantitative RT-PCR in this application. The
proteome has been analyzed in part by 2 dimensional SDS-PAGE and
tandem MS-MS. Understanding how this bacterium senses the presence
of a complex polysaccharide to regulate target genes in another
major thrust of this work. This latter work is being facilitated
through the use of comparative genomics with other similar
cellulolytic bacteria. Thus we are using sophisticated,
state-of-the-art techniques to understand how these enzyme systems
operate.
We are also
working with faculty and students in the Department of Materials
Science and Engineering to understand the mechanisms by which
organic liquids interact with cellulose during pretreatments. This
work should help reduce the cost of digesting biomass as less enzyme
should be required to release sugars from biomass if the right
conditions can be established during the pretreatment.
Selected Recent Publications:
-
Suvorov, M, R
Kumar, H Zhang,
and SW
Hutcheson, 2011.
Novelties of the
cellulolytic
system of a
marine bacterium
applicable to
cellulosic sugar
production.
Biofuels, In
Press
-
Watson, BJ, H
Zhang, AG
Longmire, Y-H
Moon and SW
Hutcheson,
2009.
Processive
endoglucanases
mediate
degradation of
cellulose by
Saccharophagus
degradans 2-40
J. Bacteriol.
191, 5697-5705
JB.00481-09 [pii]
10.1128/JB.00481-09
-
Weiner, R, L
Taylor, B
Henrissat, L
Hauser, M Land,
P Coutinho, C
Rancurel, E
Saunders, A
Longmire, H
Zhang, E Bayer,
H Gilbert, F
Larimer, I
Zhulin, N Ekborg,
R Lamed, P
Richardson, I
Borovok, and S
Hutcheson, 2008.
Complete genome
sequence of the
complex
carbohydrate-degrading
marine
bacterium,
Saccharophagus
degradans Strain
2-40. PLOS
Genetics 4 |
e1000087.
doi:10.1371/journal.pgen.1000087
-
Henshaw, J, V.
Money, D. Bolam,
M. Czjzek, N.
Ekborg, R.
Weiner, S.
Hutcheson, G.J.
Davies, HJ.
Gilbert and AB.
Boraston, 2006.
Family 6
Carbohydrate
Binding Modules
in-Agarases
Display
Exquisite
Selectivity for
the Non-Reducing
Termini of
Agarose, J.
Biol. Chem.
281:17099-17107
doi:10.1074/jbc.M600702200
-
Taylor, L, B
Henrissat, N
Ekborg, M
Howard, S
Hutcheson, and R
Weiner. 2006.
Analysis of the
unusually
abundant enzymes
and auxiliary
proteins of a
marine
bacterium,
strain 2-40,
linked to plant
cell wall
degradation. J.
Bacteriol. 188,
3849-3861
doi:10.1128/JB.01348-05
-
Howard, MB, N
Ekborg, L.
Taylor, R.
Weiner and SW
Hutcheson, 2004.
Chitinase B of
Microbulbifer
degradans 2-40
contains two
catalytic
domains with
different
chitinolytic
activities. J.
Bacteriology
186: 1297-1303
doi:
10.1128/JB.186.5.1297-1303.2004
| |