@ARTICLE{TreeBASE2Ref14914,
author = {Barbara J Campbell and S. Craig Cary},
title = {Abundance of Reverse Tricarboxylic Acid Cycle Genes in Free-Living Microorganisms at Deep-Sea Hydrothermal Vents},
year = {2004},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Applied and Environmental Microbiology},
volume = {70},
number = {},
pages = {},
abstract = {Since the discovery of hydrothermal vents over 25 years ago, the Calvin-Bassham-Benson (Calvin) cycle has been considered to be the principal carbon fixation pathway in this microbial-based ecosystem. However, based on recent molecular data of cultured free-living and non-cultured episymbiotic members of the epsilon subdivision of Proteobacteria and earlier carbon isotope data of primary consumers, an alternative autotrophic pathway may predominate. Here, genetic and culture-based approaches demonstrated the abundance of the reverse tricarboxylic acid cycle compared to the Calvin cycle in microbial communities from two geographically distinct deep-sea hydrothermal vents. PCR with degenerate primers for three key genes in the reverse tricarboxylic acid cycle as well as form I and form II of ribulose 1,5-bisphosphate carboxylase/oxygenase (Calvin cycle marker gene) was utilized to demonstrate the abundance of the reverse tricarboxylic acid cycle in diverse vent samples. These genes were also expressed in at least one chimney sample. Diversity, similarity matrix and phylogenetic analyses of cloned samples as well as amplified gene products from autotrophic enrichment cultures suggest that the majority of autotrophs that utilize the reverse tricarboxylic acid cycle are members of the epsilon Proteobacteria. These results parallel previously published 16S molecular surveys which demonstrate the dominance of epsilon Proteobacteria in free-living hydrothermal vent communities. Epsilon Proteobacteria are ubiquitous in many other microaerophilic to anaerobic sulfidic environments as well, such as the deep subsurface. Therefore, the reverse tricarboxylic acid cycle may be a major autotrophic pathway in these environments and significantly contribute to global autotrophic processes.}
}
Taxa for Study 1244

Citation title:
"Abundance of Reverse Tricarboxylic Acid Cycle Genes in Free-Living Microorganisms at Deep-Sea Hydrothermal Vents".

This study was previously identified under the legacy study ID S1158
(Status: Published).
Taxa
ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
63638 |
1f Guaymas |
|
|
3802 |
2B09 Guaymas |
|
|
3798 |
2a09 Guaymas |
|
|
3826 |
2a10 Guaymas |
|
|
3805 |
2b10 Guaymas |
|
|
63648 |
2d Guaymas |
|
|
3814 |
2e08 Guaymas |
|
|
3807 |
2e09 Guaymas |
|
|
3820 |
2e10 Guaymas |
|
|
63629 |
2f Guaymas |
|
|
3831 |
2f08 Guaymas |
|
|
3827 |
2f10 Guaymas |
|
|
3804 |
2g10 Guaymas |
|
|
3806 |
2h07 Guaymas |
|
|
3801 |
2h09 Guaymas |
|
|
3829 |
3833-42 enrichment |
|
|
62923 |
3838 RT |
|
|
3799 |
3838-RT enrichment |
|
|
63665 |
3E Guaymas |
|
|
63632 |
3H Guaymas |
|
|
63636 |
4a Guaymas |
|
|
63659 |
6A Guaymas |
|
|
63639 |
6B Guaymas |
|
|
63664 |
807 21 Guaymas |
|
|
63663 |
807 22 Guaymas |
|
|
63653 |
807 28 POB |
|
|
3821 |
820-A10 POB 9N |
|
|
3819 |
820-A11 POB 9N |
|
|
3818 |
820-A12 POB 9N |
|
|
3817 |
820-A6 POB-9N |
|
|
3822 |
820-B11 POB 9N |
|
|
3823 |
820-C1 POB 9N |
|
|
3809 |
820-C11 POB 9N |
|
|
3825 |
820-C7 POB 9N |
|
|
3824 |
820-D2 POB 9N |
|
|
3810 |
820-D5 POB 9N |
|
|
3803 |
820-D8 POB 9N |
|
|
3815 |
827-2 Guaymas |
|
|
3797 |
827-3 Guaymas |
|
|
3811 |
827-5 Guaymas |
|
|
3830 |
828-2 Guaymas |
|
|
68133 |
840-1 E3 POB 9N |
|
|
68129 |
840-2 F3 POB 9N |
|
|
68123 |
840-3 A4 POB 9N |
|
|
68128 |
840-4 G5 POB 9N |
|
|
64749 |
846-4-Guaymas |
|
|
68131 |
847-2 Guaymas |
|
|
64755 |
847-3-POB 9N |
|
|
63628 |
848-2 Guaymas |
|
|
63645 |
A05 Guaymas |
|
|
68127 |
A07 Guaymas |
|
|
64761 |
A10-Guaymas |
|
|
63657 |
A11 POB 9N |
|
|
3812 |
A5 POB 9N |
|
|
62931 |
Alcaligenes eutrophus |
106590
|
3865782
|
3800 |
Alvinella pompejana symbiont |
6376
|
5326346
|
63637 |
Archeoglobus fuligidus |
224325
|
5325437
|
63631 |
B02 Guaymas |
|
|
68125 |
B04 POB 9N |
|
|
68122 |
B06 Guaymas |
|
|
68121 |
B07 Guaymas |
|
|
64760 |
B08-POB-9N |
|
|
63627 |
B10 POB 9N |
|
|
64763 |
B10-Guaymas |
|
|
63650 |
B11 POB 9N |
|
|
63649 |
B12 POB 9N |
|
|
63655 |
C01 Guaymas |
|
|
63662 |
C04 Guaymas |
|
|
63654 |
C05 Guaymas |
|
|
68126 |
C07 Guaymas |
|
|
64757 |
C08-Guaymas |
|
|
64747 |
C08-POB-9N |
|
|
64756 |
C09-Guaymas |
|
|
63658 |
C10 POB 9N |
|
|
151479 |
Campylobacter jejuni |
197
|
229785
|
3808 |
Candidatus Arcobacter sulfidicus |
28196
|
2554051
|
3828 |
Chlorobium limicola |
290315
|
5325516
|
151535 |
Chlorobium tepidum |
1097
|
2554837
|
68130 |
Chorobium tepidum |
1097
|
2554837
|
63646 |
D02 Guaymas |
|
|
63630 |
D03 Guaymas |
|
|
68124 |
D06 Guaymas |
|
|
64752 |
D08-POB-9N |
|
|
64753 |
D09-Guaymas |
|
|
64759 |
D10-Guaymas |
|
|
64748 |
D7-Guaymas |
|
|
68132 |
Desulfovibrio desulfuricans G20 |
876
|
229796
|
63647 |
E05 Guaymas |
|
|
63643 |
E06 Guaymas |
|
|
64750 |
E08-POB-9N |
|
|
63635 |
E09 POB 9N |
|
|
64758 |
E09-Guaymas |
|
|
63660 |
E12 POB 9N |
|
|
151555 |
Escherichia coli |
562
|
2555646
|
63652 |
F03 Guaymas |
|
|
63651 |
F04 Guaymas |
|
|
64751 |
F09-Guaymas |
|
|
63641 |
F12 POB 9N |
|
|
62926 |
FII B1 POB 9N |
|
|
62929 |
FII C1 POB 9N |
|
|
62922 |
FII C3 POB 9N |
|
|
62908 |
FII E1 POB 9N |
|
|
62909 |
FII E4 POB 9N |
|
|
62907 |
FII F1 POB 9N |
|
|
62928 |
FII G02 POB 9N |
|
|
62934 |
FII f6 POB 9N |
|
|
68120 |
G03 POB 9N |
|
|
64762 |
G08-POB-9N |
|
|
63656 |
G09 POB 9N |
|
|
64754 |
G09-Guyamas |
|
|
63633 |
G10 POB 9N |
|
|
63661 |
G11 POB 9N |
|
|
151562 |
Geobacter metallireducens |
28232
|
2555916
|
63640 |
H02 Guaymas |
|
|
63644 |
H03 Guaymas |
|
|
63634 |
H10 POB 9N |
|
|
63642 |
H11 POB 9N |
|
|
151590 |
Helicobacter pylori |
210
|
2556161
|
8652 |
Hydrogenobacter thermophilus |
940
|
2556212
|
62918 |
Hydrogenophilus thermoluteolus |
297
|
2556223
|
62916 |
Hydrogenovibrio marinus |
28885
|
2556227
|
151516 |
Methanococcus jannaschii |
243232
|
5325698
|
3816 |
Nautilia sp. AmH |
191291
|
3017536
|
3813 |
Persephonella marina |
123214
|
3017599
|
62910 |
Pogonophora sp. JT1 endosymbiont |
27906
|
216542
|
15606 |
Pyrococcus furiosus |
2261
|
2558177
|
62912 |
Rhodobacter capsula |
|
|
62919 |
Rhodobacter veldkampii |
33049
|
2558235
|
62917 |
Rhodspirillum rubrum |
1085
|
3865983
|
62925 |
Riftia pachyptila endosymbiont |
54396
|
10146171
|
68119 |
Salmonella typhimurium |
90371
|
2558477
|
62906 |
Synechococcus sp. WH7803 |
1129
|
2560121
|
151556 |
Thiobacillus denitrificans |
36861
|
2559707
|
62936 |
Thiobacillus denitrificans b |
36861
|
2559707
|
62927 |
Thiobacillus ferrooxidans |
243159
|
2559708
|
62915 |
Thiobacillus sp. |
919
|
2559700
|
62911 |
Uncultured bacteria SBII-2 |
|
|
62920 |
a05 POB 9N |
|
|
62924 |
c04 POB 9N |
|
|
62930 |
c07 POB 9N |
|
|
62933 |
d05 POB 9N |
|
|
62921 |
e05 POB 9N |
|
|
62914 |
f06 POB 9N |
|
|
62913 |
g05 POB 9N |
|
|
62932 |
h04 POB 9N |
|
|