Table 1.
I. album | “Ca. T. aerophilum”a | C. thalassium | Chlorobiaceae | |
---|---|---|---|---|
Genome size (Mb) | 3.66 | 3.18 | 3.29 | 1.97–3.13 |
Photosynthetic apparatus | No | Yes | Yes | Yes |
Relationship with O2 | Oxic and anoxic | Oxic | Anoxic | Anoxic |
Reverse TCA cycle | Incompleteb | Incomplete | Yes | Yes |
PFOR and KFORc | Yes | Yes | Yes | Yes |
RNF complex | Yes | No | No | Some |
Type-1 NADH dehydrogenase | Two copies (14 and 11 SU)d | Two copies (12 and 11 SU)d | Two copies (14 and 11 SU)d | One copy (11 SU)d |
Complex III | ACIIIe | Both ACIIIe and Cyt b-Rieske | Cyt b-Rieske | Cyt b-Rieske |
Terminal oxidases | Cyt caa3, cbb3, bd(1), bd(2)f | Cyt caa3 | Cyt bd(2) | Cyt cbb3 and/or bd(1) |
Flagella genes | Yes | No | No | No |
Chemotaxis genes | Yes | Partial | Partial | No |
Sulfide oxidation to polysulfide | Yes | No | Yes | Yes |
Sulfur oxidation to sulfite | No | No | Nog | Mostg |
Nitrogen fixation | No | No | Yes | Yes |
aInferences made from metagenome and metatranscriptome data (Liu et al., 2012). Additional genes could be present in the organism.
bI. album lacks ATP citrate lyase to have a complete reverse TCA cycle. It is possible that (ATP-independent) citrate lyase enables an unconventional reverse TCA cycle under certain growth conditions.
cPFOR, pyruvate:ferredoxin oxidoreductase; KFOR, 2-oxoglutarate:ferredoxin oxidoreductase
dSU, subunits.
eACIII, alternative complex III.
fTwo different cytochrome bd-quinol oxidases exist among Chlorobi. See Figures 6 and 8B for details.
gMost organisms belonging to the Chlorobiaceae have genes involved in oxidation of sulfide to sulfate, with a few exceptions (see Gregersen et al., 2011).