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. 2005 Oct;71(10):6104–6114. doi: 10.1128/AEM.71.10.6104-6114.2005

TABLE 3.

Growth of C. glutamicum strains with deletions in ssu and seu genes on different classes of sulfonates and sulfonate estersa

Compound Growth of strains
Wild type ΔssuA or ΔssuB or ΔssuC (transporter)b,c ΔssuD1 (monooxy- genase)c ΔssuD2 (monooxy- genase)c ΔssuD1 ΔssuD2 (monooxy- genases)c,d ΔseuA or ΔseuB (monooxy- genase)b,c ΔseuC (monooxy- genase)c ΔssuD1 ΔssuD2 ΔseuABC (monooxy- genases)c,d ΔssuI (reductase)c
Inorganic sulfur compounds
    Sulfate, sulfite + + + + + + + + +
Sulfonates
    Simple aliphatic sulfonates (e.g., ethanesulfonate) + + + + +
    Long-chain simple aliphatic sulfonates (e.g., octanesulfonate) + + + + + +
    Organic buffers (e.g., MOPS) + + + + +
    Aliphatic sulfonates with additional group (e.g., taurine) + e + + +
Sulfonate esters
    Busulfan + + + + + + +
    Butanesultone + + + + + +
    (S)-1,2,4-Butanetriol-trimethane-sulfonate + + + + +
    Ethyl methanesulfonate + + + + + + +
    l-(−)-Methanesulfonylethyllactate + + + + + + +
    Methyl methanesulfonate + + + + + + +
    Propanesultone + + + + +
a

+, compound can be used as a sole sulfur source; −, growth was the same as the growth with no added sulfur after 72 h of incubation at 30°C. The test substances are shown in Fig. 1. Only compounds that could be utilized as sulfur sources by the wild type were used for the growth tests.

b

Strains having a deletion in any of the genes had the same phenotype.

c

The data in parentheses are the proposed functions of the deleted genes.

d

A strain having multiple deletions was constructed and tested.

e

Deletion of ssuD1 resulted in a mutant able to utilize all sulfonates except l-cysteic acid, 1,2-ethanedisulfonate, and sulfoacetate.