Dobritzsch, D., Konig, S., Schneider, G., & Lu, G. High resolution crystal structure of pyruvate
decarboxylase from Zymomonas mobilis – implications for substrate activation in
pyruvate decarboxylases. The Journal of Biological Chemistry. 1998
The
authors present a crystal structure of pyruvate decarboxylase (PDC) from the Zymomonas mobilis bacterium. The presented PDC is one that has yet to be
observed. The pyruvate decarboxylase
from the bacterium, ZmPDC, was determined by molecular displacement methods. ZmPDC is a homotetramer. Each monomer can be further divided into
three domains: PYR, R, and PP. Each
domain has open alpha/beta topology. At
the dimer-dimer interface, they interpreted some residual electron density as
citrate molecules. The four citrates
might contribute to the tetramer assembly by electrostatic interactions and
hydrogen bonds to protein side chains. A
quaternary structure comparison of PDC from Z.
mobilis and PDC from yeast shows structural differences that may be related
to the differences in their kinetic behavior.
Hokyoung S., Kyunghun M., Jungkwan, L. , Gyung, J.,
Jin-Cheol K., & Yin-Won, L.
Differential roles of pyruvate decarboxylase in aerial and embedded
mycelia of the ascomycete Giberrela zeae.
FEMS Microbiology Letters. 2012
The
researchers knocked out the three PDC genes in the fungus Giberrela zeae. In
particular, they looked at PDC1 and its role in the
pyruvate-acetaldehyde-acetate (PAA) pathway.
The PAA pathway is important for its role in lipid production. When PDC1 was knocked out, lipid accumulation
declined in the aerial, but not the embedded mycelia. Therefore, PDC1 may function as a key enzyme
in lipid production in the aerial mycelia, and it mat function differently in
the embedded mycelia, where it is believed to be involved in energy generation
by ethanol fermentation. This is the
first description of different physiological roles in the aerial and embedded
mycelia for the same metabolic process in filamentous fungi. PDC1 and the PPA pathway are important for
lipid production in the aerial mycelia.
However, embedded mycelia seem to utilize them via ethanol fermentation
for growth.
Kondo, T., Tezuka, H., Ishii, J., Matsuda, F., Ogino, C.,
and Kondo, A. Genetic engineering to
enhance the Ehrlich pathway and alter carbon flux for increased isobutanol
production from glucose by Saccharomyces cerevisiae. Journal
of Biotechnology. 2012
Recently, much attention has been
given to the production of higher alcohols by engineered bacteria. Saccharomyces
cerevisiae has much potential as a producer of alcohols due to its
tolerance to low pH among other things. Since
the bacterium does not naturally produce alcohols significantly, the
researchers sought to genetically engineer a way to increase production of the
alcohol isobutanol. Knocking out the
PDC1 gene (see above), along with modification of culture conditions and
enhancing the Ehrlich pathway, resulted in a 13-fold increase in isobutanol
concentration. The Ehrlich pathway was
enhanced by overexpressing 2-keto acid decarboxylase, alcohol dehydrogenase,
and IIv2.
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