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. 2022 Mar 10;23(6):2992. doi: 10.3390/ijms23062992

Table 1.

Kinetic analysis of recombinant β-D-xylosidases from L. reuteri and B. producta strains using pNP-Xyl as substrate, determined in 50 mM sodium phosphate buffer (pH 5.7) at 45 °C.

Enzyme Km (mM) kcat (s−1) kcat/Km (s−1mM−1)
Bp- XylX-1 0.19 ± 0.02 11.9 ± 0.23 63
Bp-XylX-2 0.19 ± 0.02 10.7 ± 0.2 56
Lr-XylC 0.23 ± 0.02 11.4 ± 0.2 49
Bp-XylX-1-D371 0 0 0
Bp-XylX-1-E408 0 0 0
Bp-XylX-2-D386 0 0 0
Bp-XylX-2-E409 0 0 0
LR-XylC -D382 0 0 0
LR-XylC -E415 0 0 0