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. 2017 Mar 15;101(12):5163–5173. doi: 10.1007/s00253-017-8212-x

Table 1.

Identification of obtained isolates and growth observations with SLES, under nitrate-reducing conditions

Strain code Identification Growtha Enrichmentb
S1 Aeromonas hydrophila (99% similar to A. hydrophila DSM 30187T) +/− 50
S3 A. hydrophila (99% similar to A. hydrophila DSM 30187T) +/− 250
S6 Pseudomonas nitroreducens (99% similar to P. nitroreducens DSM 14399T) +/− 250
S7 A. hydrophila (99% similar to A. hydrophila DSM 30187T) +/− 250
S8 Pseudomonas stutzeri (99% similar to P. stutzeri CCUG 11256T) + 1000
S10 P. stutzeri (99% similar to P. stutzeri CCUG 11256T) + 1000
S11 P. nitroreducens (99% similar to P. nitroreducens DSM 14399T) + 1000

Based on 16S rRNA gene comparison (http://ncbi.nlm.nih.gov/blast), strains S1, S3, and S7 are 99% similar; strains S6 and S11 are 99% similar; strains S8 and S10 are 99% similar. All strains were also tested for SLES degradation with oxygen as electron acceptor; similar growth observations were obtained as presented in this table

aGrowth observations were compared to controls without SLES; +/− weak but visible growth; + growth

bOriginal enrichment where the strain was isolated from; 50, 250, and 1000 correspond to the 50, 250, and 1000 mg SLES L−1 enrichments, respectively