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Most bacteria contain soluble quinone-reducing flavoenzymes.
It is now understood that most bacteria contain genes coding for the formation of density-dependent quorum sensing systems [4] [7].
Most bacteria contain multiple homologs of this transcription factor family.
Most bacteria contain less than 14 TBDPs in their proteome, although some bacteria have larger numbers [ 32].
Endo V was originally reported as a DNA repair enzyme [ 43, 44, 63] encoded by the nfi gene; most bacteria contain the nfi gene in their genome.
The proteins fell into six classes whereas most bacteria contain at most five well separated clusters with bayesian clustering and at most four with dynamic clouds clustering [ 14].
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Moreover, these results reveal that most bacteria containing FADS-type II sequences have also typical FADS-type I proteins (see Table 1) and the tree in Figure 3 shows that these two types of sequences cluster together, implying that they might actually be paralogous genes.
In contrast, most Gram-positive bacteria contain a "minimal" TatAC machinery that lacks the TatB protein [18], [19].
In contrast to the GOS data, only two of the genomes of the most common marine bacteria contain peroxidases.
Most Gram-negative bacteria contain smooth LPS, which due to the long polysaccharide chain are very water-soluble when purified.
Though most bacteria that contain IcmF clusters are pathogenic agents that associate with eukaryotic cell hosts [ 54], it has been reported that the host interactions supported by this cluster are not restricted to pathogens [ 55].
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