TABLE 2.
Species | Strain(s) | PCR detection of lnpAe | Growth ond: |
Type of activityc,e |
||||
---|---|---|---|---|---|---|---|---|
LNB phosphorolyzinga |
LNB formingb |
|||||||
Glucose | LNB | Glucose | LNB | Glucose | LNB | |||
B. pseudocatenulatum | IV-152 (same as ATCC 27919T) | − | 5 | 5 | − | − | − | − |
ATCC 27677 | − | 5 | 4 | − | − | − | − | |
ATCC 27676 | − | 4 | 4 | − | − | − | − | |
MCC 0310 | − | 5 | 0 | − | ND | − | ND | |
MCC 0337 | − | 5 | 0 | − | ND | − | ND | |
MCC 0376 | − | 5 | 0 | − | ND | − | ND | |
B. animalis subsp. | IV-58 (same as ATCC 25527T) | − | 4 | 0 | − | ND | − | ND |
animalis | IV-124 (same as ATCC 27672) | + | 4 | 5 | − | + | − | + |
B. longum subsp. longum | IV-51 (same as ATCC 15707T) | + | 5 | 5 | − | + | − | + |
B. longum subsp. infantis | IV-8 (same as ATCC 15697T) | + | 5 | 5 | − | + | − | + |
B. breve | IV-14 (same as ATCC 15700T) | + | 5 | 5 | + | + | + | + |
B. bifidum | IV-127 (same as ATCC 29521T) | + | 3 | 1 | + | ± | + | ± |
B. pseudolongum | IV-70 (same as ATCC 25526T) | + | 4 | 5 | − | + | − | + |
LNB-phosphorolyzing activity was indicated by the detection of Gal1P degraded from LNB in the presence of phosphate by TLC after incubation for 5 to 18 h.
LNB-forming activity was indicated by the detection of LNB formation from Gal1P and GlcNAc by TLC after incubation for 24 to 66 h.
LNB and glucose were the carbohydrate sources used in cultivating each strain for the preparation of crude cell extract.
Growth patterns as described in Table 1.
+, presence of lnpA or enzymatic activity; −, absence of lnpA or enzymatic activity; ±, weak activity; ND, not examined. Crude cell extract boiled for 10 min showed no activity (data not shown).