TY - JOUR
T1 - Increase in hydrophobicity of Bacillus subtilis spores by heat, hydrostatic pressure, and pressurized carbon dioxide treatments
AU - Noma, Seiji
AU - Kiyohara, Kazuki
AU - Hirokado, Rina
AU - Yamashita, Nami
AU - Migita, Yuya
AU - Tanaka, Motoharu
AU - Furukawa, Soichi
AU - Ogihara, Hirokazu
AU - Morinaga, Yasushi
AU - Igura, Noriyuki
AU - Shimoda, Mitsuya
N1 - Funding Information:
A part of this work was supported by the Japan Society for the Promotion of Science (grant number 26350094 ). Measurement of zeta potential was supported by Nanotechnology Platform Project (Kyushu University Molecule and Material Synthesis Platform) Kyushu-area Nanotechnology Network) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan.
Publisher Copyright:
© 2017 The Society for Biotechnology, Japan
PY - 2018/3
Y1 - 2018/3
N2 - The effects of heat treatment (HT), hydrostatic pressure treatment (HPT), and pressurized carbon dioxide treatment (CT) on surface hydrophobicity of B. subtilis 168 spores were investigated. The spore surface hydrophobicity was measured by determining the ratio of hydrophobic spores (RHS) that were partitioned into the n-hexadecane phase from the aqueous spore suspension. The RHS after HT generally increased in a temperature-dependent manner and reached approximately 10% at temperatures above 60°C. The effects of pressurization by HPT and accompanying temperature on increased RHS were complex. The highest RHS after HPT was approximately 17%. Following CT, RHS reached approximately 80% at 5 MPa at 80°C for 30 min. An increased treatment temperature enhanced RHS by CT. The increase in RHS by CT led to the formation of spore clumps and adhesion of spores to hydrophobic surfaces. Acidification of spore suspension to pH 3.2, expected pH during CT, by HCl also increased the adhesion of spores at the similar degree with CT. The spore surface zeta potential distribution was not changed by CT. Furthermore, spores with increased RHS after CT had germination-like phenomena including loss of their refractility and enhanced staining by 4′,6-diamidino-2-phenylindole. Physiological germination that was induced by the addition of L-alanine also increased the RHS. From these results, it is clear that CT under heating considerably increases RHS. CT under heating considerably increases RHS. This increase in RHS may be due to acidification or germination-like phenomena during CT.
AB - The effects of heat treatment (HT), hydrostatic pressure treatment (HPT), and pressurized carbon dioxide treatment (CT) on surface hydrophobicity of B. subtilis 168 spores were investigated. The spore surface hydrophobicity was measured by determining the ratio of hydrophobic spores (RHS) that were partitioned into the n-hexadecane phase from the aqueous spore suspension. The RHS after HT generally increased in a temperature-dependent manner and reached approximately 10% at temperatures above 60°C. The effects of pressurization by HPT and accompanying temperature on increased RHS were complex. The highest RHS after HPT was approximately 17%. Following CT, RHS reached approximately 80% at 5 MPa at 80°C for 30 min. An increased treatment temperature enhanced RHS by CT. The increase in RHS by CT led to the formation of spore clumps and adhesion of spores to hydrophobic surfaces. Acidification of spore suspension to pH 3.2, expected pH during CT, by HCl also increased the adhesion of spores at the similar degree with CT. The spore surface zeta potential distribution was not changed by CT. Furthermore, spores with increased RHS after CT had germination-like phenomena including loss of their refractility and enhanced staining by 4′,6-diamidino-2-phenylindole. Physiological germination that was induced by the addition of L-alanine also increased the RHS. From these results, it is clear that CT under heating considerably increases RHS. CT under heating considerably increases RHS. This increase in RHS may be due to acidification or germination-like phenomena during CT.
UR - http://www.scopus.com/inward/record.url?scp=85032330696&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85032330696&partnerID=8YFLogxK
U2 - 10.1016/j.jbiosc.2017.09.012
DO - 10.1016/j.jbiosc.2017.09.012
M3 - Article
C2 - 29107628
AN - SCOPUS:85032330696
SN - 1389-1723
VL - 125
SP - 327
EP - 332
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 3
ER -