TY - JOUR
T1 - Development of enzyme cocktails for complete saccharification of chitin using mono-component enzymes from Serratia marcescens
AU - Mekasha, Sophanit
AU - Byman, Ida Roksvåg
AU - Lynch, Catherine
AU - Toupalová, Hana
AU - Anděra, Ladislav
AU - Næs, Tormod
AU - Vaaje-Kolstad, Gustav
AU - Eijsink, Vincent G.H.
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/5/1
Y1 - 2017/5/1
N2 - One potential strategy for biorefining of chitin-rich biomass entails enzymatic saccharification, which, so far, has been scarcely explored. Here, saccharification of chitin was explored using response surface methodology available in the MODDE®10 software, to develop optimal cocktails of five mono-component enzymes from Serratia marcescens, three chitinases, SmChiA, SmChiB, SmChiC, a lytic polysaccharide monooxygenase, SmLPMO10A (or “CBP21”), and a beta-N-acetylhexosaminidase, SmCHB (“chitobiase”). These five enzymes were recombinantly produced in Escherichia coli. For both shrimp and crab chitins, SmChiA was the most abundant (40% and 38%, respectively) in the optimized cocktails, whereas SmChiB, SmChiC and SmLPMO10A were present at 30% and 26%, 15% and 23%, and 3% and 2%, respectively. Saccharification yields were 70%–75%, whereas a “minimal” cocktail of SmChiA and SmCHB gave only 40% saccharification. These results show that enzymatic saccharification of chitin requires multiple enzyme activities applied at dosages similar to those used for saccharification of cellulose.
AB - One potential strategy for biorefining of chitin-rich biomass entails enzymatic saccharification, which, so far, has been scarcely explored. Here, saccharification of chitin was explored using response surface methodology available in the MODDE®10 software, to develop optimal cocktails of five mono-component enzymes from Serratia marcescens, three chitinases, SmChiA, SmChiB, SmChiC, a lytic polysaccharide monooxygenase, SmLPMO10A (or “CBP21”), and a beta-N-acetylhexosaminidase, SmCHB (“chitobiase”). These five enzymes were recombinantly produced in Escherichia coli. For both shrimp and crab chitins, SmChiA was the most abundant (40% and 38%, respectively) in the optimized cocktails, whereas SmChiB, SmChiC and SmLPMO10A were present at 30% and 26%, 15% and 23%, and 3% and 2%, respectively. Saccharification yields were 70%–75%, whereas a “minimal” cocktail of SmChiA and SmCHB gave only 40% saccharification. These results show that enzymatic saccharification of chitin requires multiple enzyme activities applied at dosages similar to those used for saccharification of cellulose.
KW - Chitin
KW - Chitinases
KW - Response surface methodology
KW - Saccharification
KW - Serratia marcescens
UR - http://www.scopus.com/inward/record.url?scp=85014386177&partnerID=8YFLogxK
U2 - 10.1016/j.procbio.2017.02.021
DO - 10.1016/j.procbio.2017.02.021
M3 - Article
AN - SCOPUS:85014386177
SN - 1359-5113
VL - 56
SP - 132
EP - 138
JO - Process Biochemistry
JF - Process Biochemistry
ER -