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Similarly, the ß' subunit of proteobacteria, Aquifex , spirochaetes, cyanobacteria and chlamydiae contains an additional set of SBHMs C-terminal of the DPBB domain, preceding the C-terminal SBHM that is shared by all bacteria (Fig.

Proteobacteria, Aquifex , spirochetes and chlamydiae have a BBM2 inserted into the N-terminal region of the ß subunit (Fig.

txt Background Chlamydiae are obligate intracellular pathogens that infect a variety of host organisms and exhibit individual tissue tropisms within a host species.

A number of analyses dealing with the comparative genomics of the chlamydiae have appeared in the recent literature [ 1, 2, 3].

Finally, serine import is required for the tryptophan synthase step as chlamydiae are not competent for serine biosynthesis.

Deterioration of tryptophan-pathway genes in the chlamydiae Chlamydial species have generally undergone reductive evolution that includes an inability to synthesize tryptophan from chorismate.

Therefore, present-day TrpEb may function in the chlamydiae as serine deaminase, as has been proposed by Xie et al.

This is consistent with the total absence of genes in chlamydiae known to encode enzymes with serine deaminase activity.

Overview of tryptophan-pathway variability in chlamydiae Shaw et al.

Morrison [ 46] has also discussed the possible relationship of genes present or absent for tryptophan biosynthesis and the differential sensitivities of chlamydiae to inhibitory effects of IFN-?

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Chlamydial transport of tryptophan, kynurenine and serine The chlamydiae are dependent on host cells for a variety of metabolites that are relevant to the host-parasite relationships of tryptophan metabolism.

Species of chlamydiae possess one ( C.

Species of chlamydiae possess two paralogs of SstT, which were judged to be the most likely genes encoding serine transport.

fastidiosa where trpR exhibited a low GC content, more similar to that of the chlamydiae or H.

In any event, for most chlamydiae the successful implementation of tryptophan depletion by the host is closely tied to chlamydial responses that result in a persistent metabolic state and chronic disease.

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