TY - JOUR
T1 - Enhanced amylase production by a Bacillus subtilis strain under blue light-emitting diodes
AU - Elumalai, Punniyakotti
AU - Lim, Jeong Muk
AU - Park, Yool Jin
AU - Cho, Min
AU - Shea, Patrick J.
AU - Oh, Byung Taek
N1 - Funding Information:
This work was supported by the BK21 plus program through the National Research Foundation (NRF) funded by the Ministry of Education of Korea and supported by the National Research Foundation of Korea (Nano-Material Fundamental Technology Development, 2016M3A7B4909370). This work was also partially
Funding Information:
supported by Korea Ministry of Environment as Eco-Innovation Project (2016000140001).
Publisher Copyright:
© 2019, © 2019 Taylor & Francis.
PY - 2019/2/7
Y1 - 2019/2/7
N2 - A chemotrophic, aerobic bacterial strain, Bacillus subtilis B2, was used to produce amylase by submerged fermentation under different light sources. SDS-PAGE indicated that the 55 kDa enzyme belonged to the α-amylase group. B2 was incubated in basal media with 1% soluble starch (pH 7.0) under blue, green, red, and white light-emitting diodes (LEDs), and white fluorescent light. Fermentation under blue LEDs maximized amylase production (180.59 ± 1.6 U/mL at 24 h). Production at 48 h increased to 310.56 ± 1.6 U/mL with 5% glucose as a simple carbon source and to 300.51 ± 1.7 U/mL with 5% groundnut oil cake as an agricultural waste substrate. Activity and stability of the amylase were greatest at pH 7.0 and 45–55 °C. Na + , Ca 2+ , Mg 2+ , Co 2+ , Ba 2+ , and K + increased activity, while Ni 2+ , Hg 2+ , Mn 2+ , Cu 2+ , Fe 3+ , and Zn 2+ inhibited activity. EDTA, PMSF and DTNB reduced activity by 50% or more, while tetrafluoroethylene and 1,10-phenanthroline reduced activity by 30%. The amylase was highly tolerant of the surfactants, compatible with organic solvents, oxidizing agents and the reducing agents reduced activity. These properties suggest utility of amylase produced by B. subtilis B2 under blue LED-mediated fermentation for industrial applications.
AB - A chemotrophic, aerobic bacterial strain, Bacillus subtilis B2, was used to produce amylase by submerged fermentation under different light sources. SDS-PAGE indicated that the 55 kDa enzyme belonged to the α-amylase group. B2 was incubated in basal media with 1% soluble starch (pH 7.0) under blue, green, red, and white light-emitting diodes (LEDs), and white fluorescent light. Fermentation under blue LEDs maximized amylase production (180.59 ± 1.6 U/mL at 24 h). Production at 48 h increased to 310.56 ± 1.6 U/mL with 5% glucose as a simple carbon source and to 300.51 ± 1.7 U/mL with 5% groundnut oil cake as an agricultural waste substrate. Activity and stability of the amylase were greatest at pH 7.0 and 45–55 °C. Na + , Ca 2+ , Mg 2+ , Co 2+ , Ba 2+ , and K + increased activity, while Ni 2+ , Hg 2+ , Mn 2+ , Cu 2+ , Fe 3+ , and Zn 2+ inhibited activity. EDTA, PMSF and DTNB reduced activity by 50% or more, while tetrafluoroethylene and 1,10-phenanthroline reduced activity by 30%. The amylase was highly tolerant of the surfactants, compatible with organic solvents, oxidizing agents and the reducing agents reduced activity. These properties suggest utility of amylase produced by B. subtilis B2 under blue LED-mediated fermentation for industrial applications.
KW - Amylase
KW - B. subtilis
KW - blue LEDs
KW - metal ions
KW - photoreceptor
KW - surfactant
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U2 - 10.1080/10826068.2018.1550656
DO - 10.1080/10826068.2018.1550656
M3 - Article
C2 - 30636516
AN - SCOPUS:85060087312
SN - 1082-6068
VL - 49
SP - 143
EP - 150
JO - Preparative Biochemistry and Biotechnology
JF - Preparative Biochemistry and Biotechnology
IS - 2
ER -