Aerobic and anaerobic cellulose utilization by Paenibacillus sp CAA11 and enhancement of its cellulolytic ability by expressing a heterologous endoglucanase

Authors
Kim, Eun SookKim, Byeong-SooKim, Ki-YeonWoo, Han-MinLee, Sun-MiUm, Youngsoon
Issue Date
2018-02
Publisher
Elsevier BV
Citation
Journal of Biotechnology, v.268, pp.21 - 27
Abstract
For cost-effective lignocellulosic biofuel/chemical production, consolidated bioprocessing (CBP)-enabling microorganisms utilizing cellulose as well as producing biofuel/chemical are required. A novel strain Paenibacillus sp. CAA11 isolated from sediment was found to be not only as a cellulose degrader under both aerobic and strict anaerobic conditions but also as a producer of cellulosic biofuel/chemicals. Paenibacillus sp. CAA11 secreted cellulolytic enzymes by its own secretion system and produced ethanol as well as short-chain organic acids (formic acid, acetic acid, lactic acid) from cellulose. Cellulolytic activity of the strain was significantly enhanced by expressing a heterologous endoglucanase 168Cel5 from Bacillus subtilis under both aerobic and anaerobic conditions. The strain harboring the 168cel5 gene revealed 2-fold bigger halo zone on Congo-red plate and 1.75-fold more aerobic cellulose utilization in liquid medium compared with the negative control. Notably, under anaerobic conditions, the recombinant strain expressing 168Cel5 consumed 1.83-fold more cellulose (5.10 g/L) and produced 5-fold more ethanol (0.65 g/L) along with 5-fold more total acids (1.6 g/L) compared with the control, resulting 2.73-fold higher yields. This result demonstrates the potential of Paenibacillus sp. CAA11 as a suitable aerobic and anaerobic CBP-enabling microbe with cellulolytic production of ethanol and short-chain organic acids.
Keywords
CURDLANOLYTICUS STRAIN B-6; CLOSTRIDIUM-CELLULOLYTICUM; ETHANOL-PRODUCTION; ZYMOMONAS-MOBILIS; GENE; SACCHARIFICATION; SEQUENCE; ENZYMES; FERMENTATION; DEGRADATION; Cellulose; Paenibacillus; Consolidated bioprocessing; Endoglucanase
ISSN
0168-1656
URI
https://pubs.kist.re.kr/handle/201004/121750
DOI
10.1016/j.jbiotec.2018.01.007
Appears in Collections:
KIST Article > 2018
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