Clostridium ljungdahlii
is an anaerobic homoacetogen, able to ferment sugars, other organic compounds, or CO
2
/H
2
and synthesis gas (CO/H
2
). The latter feature makes it an interesting microbe for the biotech industry, as important bulk chemicals and proteins can be produced at the expense of CO
2
, thus combining industrial needs with sustained reduction of CO and CO
2
in the atmosphere. Sequencing the complete genome of
C. ljungdahlii
revealed that it comprises 4,630,065 bp and is one of the largest clostridial genomes known to date. Experimental data and in silico comparisons revealed a third mode of anaerobic homoacetogenic metabolism. Unlike other organisms such as
Moorella thermoacetica
or
Acetobacterium woodii
, neither cytochromes nor sodium ions are involved in energy generation. Instead, an Rnf system is present, by which proton translocation can be performed. An electroporation procedure has been developed to transform the organism with plasmids bearing heterologous genes for butanol production. Successful expression of these genes could be demonstrated, leading to formation of the biofuel. Thus,
C. ljungdahlii
can be used as a unique microbial production platform based on synthesis gas and carbon dioxide/hydrogen mixtures.
Propionibacterium acnes is a major inhabitant of adult human skin, where it resides within sebaceous follicles, usually as a harmless commensal although it has been implicated in acne vulgaris formation. The entire genome sequence of this Gram-positive bacterium encodes 2333 putative genes and revealed numerous gene products involved in degrading host molecules, including sialidases, neuraminidases, endoglycoceramidases, lipases, and pore-forming factors. Surface-associated and other immunogenic factors have been identified, which might be involved in triggering acne inflammation and other P. acnes-associated diseases.
The atp gene region of Clostridium acetobutylicum DSM 792 has been fully sequenced. It contains the F0F1 ATPase genes in the order atpIBEFHAGDC, whose products share high sequence homology to the respective proteins of a variety of other bacteria. It is the first such sequence available for a mesophilic Clostridium. Significant differences to other reported atp operons are a distal transcription start point 219 bp upstream of the translation start point and a second transcription initiation site (without corresponding promoter sequence) upstream of atpE, indicating posttranscriptional processing for massive expression of this gene product.
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