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. 2009 Oct 23;76(1):54–59. doi: 10.1128/AEM.01683-09

TABLE 2.

Detection of enzymatic activity of LNB phosphorylase in bifidobacterial strains

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 + +
a

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.

b

LNB-forming activity was indicated by the detection of LNB formation from Gal1P and GlcNAc by TLC after incubation for 24 to 66 h.

c

LNB and glucose were the carbohydrate sources used in cultivating each strain for the preparation of crude cell extract.

d

Growth patterns as described in Table 1.

e

+, 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).