TY - JOUR
T1 - The limited deglucosylation process of β-glucosidase in Bacillus cereus H62L for biotransforming secoisolariciresinol diglucoside into mammalian lignans
AU - Hwang, Chin Fa
AU - Wang, Hui Er
AU - Ker, Yaw Bee
AU - Peng, Chiung Chi
AU - Chen, Kuan Chou
AU - Peng, Robert Y.
N1 - Funding Information:
The authors are grateful for the financial support offered by the National Science Council of Taiwan (NSC 95-2313-B-241-005- MY2) and partially financial support offered by the National Science Council of Taiwan (NSC 97-2320-B-039-049-MY3, NSC 99-2320-B-039-034- and NSC 99-2320-B-038-011-MY3) and China Medical University (CMU 97-234).
PY - 2011/8
Y1 - 2011/8
N2 - The amount of major lignans present in the alkaline extract of the defatted flaxseed (in mg/g) is as follows: secoisolariciresinol diglucoside (SDG, 109.80), p-coumaric acid glucoside (CAG, 70.21), ferulic acid glucoside (FAG, 68.81), secoisolariciresinol (SECO, 0.49), coumaric acid (CA, 0.37), and ferulic acid (FA, 0.85). When biotransformed, SDG yields two valuable mammalian lignans (MLG): enterodiol (END) and enterolactone (ENL). Bacillus cereus strain H62-L1 was isolated and tested for the process of bioconversion. Kinetic analysis revealed the sequential reaction SDG (A) → CAG (B) → END (C) → ENL (D) to be reversible at the first step with the generalized reaction type Ak2k1Bk3Ck4D. The obtained rate coefficients were as follows: k1 = 0.001-0.028 h-1, k 2 = 0.006-0.077 h-1, k3 = 0.013 h-1, and k4 = 0.002 h-1, and the overall kinetic parameter k1/(k2 + k3) varied from 0.05 to 1.32, mostly not favoring the forward deglucosylation reaction. SDG with higher purity favored the forward reaction. In conclusion, to facilitate the production rate, we propose (i) using substrate SDG with high purity at a higher concentration; (ii) using an allosteric inhibitor to block the reverse reaction from SECO to SDG; or (iii) genetically modifying Bacillus cereus H62-L1.
AB - The amount of major lignans present in the alkaline extract of the defatted flaxseed (in mg/g) is as follows: secoisolariciresinol diglucoside (SDG, 109.80), p-coumaric acid glucoside (CAG, 70.21), ferulic acid glucoside (FAG, 68.81), secoisolariciresinol (SECO, 0.49), coumaric acid (CA, 0.37), and ferulic acid (FA, 0.85). When biotransformed, SDG yields two valuable mammalian lignans (MLG): enterodiol (END) and enterolactone (ENL). Bacillus cereus strain H62-L1 was isolated and tested for the process of bioconversion. Kinetic analysis revealed the sequential reaction SDG (A) → CAG (B) → END (C) → ENL (D) to be reversible at the first step with the generalized reaction type Ak2k1Bk3Ck4D. The obtained rate coefficients were as follows: k1 = 0.001-0.028 h-1, k 2 = 0.006-0.077 h-1, k3 = 0.013 h-1, and k4 = 0.002 h-1, and the overall kinetic parameter k1/(k2 + k3) varied from 0.05 to 1.32, mostly not favoring the forward deglucosylation reaction. SDG with higher purity favored the forward reaction. In conclusion, to facilitate the production rate, we propose (i) using substrate SDG with high purity at a higher concentration; (ii) using an allosteric inhibitor to block the reverse reaction from SECO to SDG; or (iii) genetically modifying Bacillus cereus H62-L1.
KW - Enterodiol
KW - Flaxseeds
KW - Glucosidase
KW - Mammalian lignans
KW - Secoisolariciresinol diglucoside
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U2 - 10.1016/j.procbio.2011.05.006
DO - 10.1016/j.procbio.2011.05.006
M3 - Article
AN - SCOPUS:79959953780
SN - 1359-5113
VL - 46
SP - 1632
EP - 1640
JO - Process Biochemistry
JF - Process Biochemistry
IS - 8
ER -