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. 2006 May;72(5):3504–3514. doi: 10.1128/AEM.72.5.3504-3514.2006

TABLE 2.

Substrate utilization profiles and genotypic characteristics of BTEX isolatesa

Isolate name Growth substrateb
C23O of subfamily I.2.A C23O typec ISPα typed ISPα/C23O combinationf ARDRA typeg
Benzene Toluene Ethylbenzene
IA1YICDA + + D PS2
IA1YICDB + + D PS2
3YC1b + + ND
3YC2 + + + Ae I PS2•
3YC4 + + + A I PS2•
3YBTEX2b + + + A I PS2
1XXyl1 + + + A I ND
1YC1 + + + + ND Ae PS1•
1XC2 + + + ND Ae PS2
1YXyl2 + + + + A A II PS1
1YXyl3 + + + + A A II PS1
1XBTEX3 + + + +• A• A II PS1
1XBTEX4 + + + + A• A II PS1
1YXyl1 + + + + A2 Ae II PS1
1YdBTEX2 + + + + A2 A II PS1
1XBTEX1 + + + + B A III PS1
1XB2 + + + + B A III PS1
1XC1 + + + +• C• Ae IV PS1
3YXyl2 + + +• C• Ae IV PS2
3YC5 + + + C• Ae IV PS2
3YdBTEX2 + + + + C Ee V PS2•
1YB1 + + A• C VI PS1
1YB2 + + A1 Ce VI PS1
1YB3 + + A1 C VI PS1
1YC2 + + A1 Ce VI PS1
1YC3 + + A1 C VI PS1
1YBTEX1 + + A1 C VI PS1
1YBTEX3 + + A1 C VI PS1
1YdBTEX3 + + A1 C VI PS1
3YdBTEX1b + + A1 C VI PS2
3YXyl2b + + A1 Ce VI PS2
3YXyl3 + + A1 C VI PS2
3YXyl1 + + + A1 Ce VI PS2
1XB1 + + A• C**e VII PS3
3YC3 + Be VIII AR•
1XXyl1b + De IX SP•
a

Data on substrate utilization, presence/type of C23O gene, and ARDRA type were reported previously (37); data indicated by • were obtained in this study by using previously reported procedures (36, 37).

b

+, growth on substrate vapor; −, no growth on substrate vapor.

c

C23O types marked by • were identified by AFDRA as reported previously (36), whereas all other C23O types were previously identified by using both AFDRA and DNA sequencing (37). ND, not determined.

d

ISPα type was determined by sequencing of reamplified SSCP products; −, no PCR product.

e

ISPα sequence was also determined by sequencing of cloned PCR products amplified with primers bphAf371B and bphAr1153-2.

f

Roman numerals are used to distinguish between different combinations of C230 and ISPα genotypes observed in a given isolate.

g

The major portion of isolates from the highly contaminated site 1 was closely related to Pseudomonas veronii CIP 104663 (AF064460, ARDRA profile PS1), whereas isolates from the slightly contaminated site 3 were predominantly related to Pseudomonas mandelii CIP 105273 (AF058286, ARDRA profile PS2). Strain 3YC3 exhibited an ARDRA fingerprint identical to those of previously analyzed Arthrobacter isolates (e.g., AY512644) and was thus considered to be a member of the genus Arthrobacter. Strain 1XXyl1b had previously been identified as a member of the genus Sphingomonas (AY512601) (34).