TY - JOUR
T1 - Characterisation of novel biomass degradation enzymes from the genome of Cellulomonas fimi
AU - Kane, Steven D.
AU - French, Christopher E.
N1 - This work was supported by the Biotechnology and Biological Sciences Research Council (Grant numbers BB/D526210/1 and BB/F017073/1). BglX CHU2268 was kindly donated by Chao-Kuo Liu.
PY - 2018/6/1
Y1 - 2018/6/1
N2 - Recent analyses of genome sequences belonging to cellulolytic bacteria have revealed many genes potentially coding for cellulosic biomass degradation enzymes. Annotation of these genes however, is based on few biochemically characterised examples. Here we present a simple strategy based on BioBricks for the rapid screening of candidate genes expressed in Escherichia coli. As proof of principle we identified over 70 putative biomass degrading genes from bacterium Cellulomonas fimi, expressing a subset of these in BioBrick format. Six novel genes showed activity in E. coli. Four interesting enzymes were characterised further. α-L-arabinofuranosidase AfsB, β-xylosidases BxyF and BxyH and multi-functional β-cellobiosidase/xylosidase XynF were partially purified to determine their optimum pH, temperature and kinetic parameters. One of these enzymes, BxyH, was unexpectedly found to be highly active at strong alkaline pH and at temperatures as high as 100 °C. This report demonstrates a simple method of quickly screening and characterising putative genes as BioBricks.
AB - Recent analyses of genome sequences belonging to cellulolytic bacteria have revealed many genes potentially coding for cellulosic biomass degradation enzymes. Annotation of these genes however, is based on few biochemically characterised examples. Here we present a simple strategy based on BioBricks for the rapid screening of candidate genes expressed in Escherichia coli. As proof of principle we identified over 70 putative biomass degrading genes from bacterium Cellulomonas fimi, expressing a subset of these in BioBrick format. Six novel genes showed activity in E. coli. Four interesting enzymes were characterised further. α-L-arabinofuranosidase AfsB, β-xylosidases BxyF and BxyH and multi-functional β-cellobiosidase/xylosidase XynF were partially purified to determine their optimum pH, temperature and kinetic parameters. One of these enzymes, BxyH, was unexpectedly found to be highly active at strong alkaline pH and at temperatures as high as 100 °C. This report demonstrates a simple method of quickly screening and characterising putative genes as BioBricks.
KW - Arabinofuranosidase
KW - C. fimi
KW - Multifunctional endoxylanase
KW - Thermotolerant xylosidase
UR - http://www.scopus.com/inward/record.url?scp=85042359141&partnerID=8YFLogxK
U2 - 10.1016/j.enzmictec.2018.02.004
DO - 10.1016/j.enzmictec.2018.02.004
M3 - Article
AN - SCOPUS:85042359141
SN - 0141-0229
VL - 113
SP - 9
EP - 17
JO - Enzyme and Microbial Technology
JF - Enzyme and Microbial Technology
ER -