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Journal of Bacteriology, July 2001, p. 4305-4316, Vol. 183, No. 14
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.14.4305-4316.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Autotrophic CO2 Fixation by Chloroflexus
aurantiacus: Study of Glyoxylate Formation and Assimilation via
the 3-Hydroxypropionate Cycle
Sylvia
Herter,1
Jan
Farfsing,1
Nasser
Gad'On,1
Christoph
Rieder,2
Wolfgang
Eisenreich,2
Adelbert
Bacher,2 and
Georg
Fuchs1,*
Mikrobiologie, Institut Biologie II,
Universität Freiburg, Freiburg,1 and
Organische Chemie und Biochemie, Technische
Universität München, Munich,2
Germany
Received 12 January 2001/Accepted 20 April 2001
In the facultative autotrophic organism Chloroflexus
aurantiacus, a phototrophic green nonsulfur bacterium, the
Calvin cycle does not appear to be operative in autotrophic carbon
assimilation. An alternative cyclic pathway, the 3-hydroxypropionate
cycle, has been proposed. In this pathway, acetyl coenzyme A
(acetyl-CoA) is assumed to be converted to malate, and two
CO2 molecules are thereby fixed. Malyl-CoA is
supposed to be cleaved to acetyl-CoA, the starting molecule, and
glyoxylate, the carbon fixation product. Malyl-CoA cleavage is
shown here to be catalyzed by malyl-CoA lyase; this enzyme activity is
induced severalfold in autotrophically grown cells. Malate is converted
to malyl-CoA via an inducible CoA transferase with succinyl-CoA as a
CoA donor. Some enzyme activities involved in the conversion of
malonyl-CoA via 3-hydroxypropionate to propionyl-CoA are also induced
under autotrophic growth conditions. So far, no clue as to the first
step in glyoxylate assimilation has been obtained. One
possibility for the assimilation of glyoxylate involves the
conversion of glyoxylate to glycine and the subsequent assimilation of glycine. However, such a pathway does not occur, as
shown by labeling of whole cells with
[1,2-13C2]glycine. Glycine carbon was
incorporated only into glycine, serine, and compounds that contained
C1 units derived therefrom and not into other cell compounds.
*
Corresponding author. Mailing address: Mikrobiologie,
Institut Biologie II, Schänzlestrasse 1, D-79104 Freiburg,
Germany. Phone: 49-761-2032649. Fax: 49-761-2032626. E-mail:
fuchsgeo{at}uni-freiburg.de.
Journal of Bacteriology, July 2001, p. 4305-4316, Vol. 183, No. 14
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.14.4305-4316.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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