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. 2001 Mar;67(3):1052–1062. doi: 10.1128/AEM.67.3.1052-1062.2001

TABLE 5.

Strains isolated from enrichment cultures and their capacity to desulfurize DBT

Strain Enriched and isolated from: Species bya:
SIb dsz genes presentc Desulfurization capacity (%)d
Sequence FAME
A36 A soil R. erythropolis R. erythropolis 0.503 dszABC 63
A61 A soil R. erythropolis dszABC 25
A69 A soil R. erythropolis R. erythropolis 0.489 dszABC 78
A74 A soil R. erythropolis 0.584 dszAB 64
A96 A soil R. erythropolis R. erythropolis 0.489 dszABC 20
M39 FSL + DBT R. erythropolis R. erythropolis 0.136 dszABC 53
M41 FSL + DBT R. erythropolis R. erythropolis 0.136 dszABC 14
A66 A soil NI dszAB 33
A73 A soil NI dszAB ND
M16 FSL + DBT S. maltophilia dszB  4
M26 FSL + DBT S. maltophilia dszB  3
a

Sequence, match on DGGE with products of R. erythropolis and S. maltophilia; FAME, closest relative from FAME database; NI, not identified. 

b

SI, similarity index, the level of similarity to closest hit of FAME database. 

c

As evidenced by PCR with dszA-, dszB-, and dszC-specific PCR systems. 

d

The percentage of DBT transformed, under standard conditions, into products by the IGTS8 pathway. R. erythropolis IGTS8 used as the positive control, transformed >25% of DBT under these conditions. ND, not determined.