TY - JOUR
T1 - Aggregation-Based Bacterial Separation with Gram-Positive Selectivity by Using a Benzoxaborole-Modified Dendrimer
AU - Mikagi, Ayame
AU - Takahashi, Yotaro
AU - Kanzawa, Nobuyuki
AU - Suzuki, Yota
AU - Tsuchido, Yuji
AU - Hashimoto, Takeshi
AU - Hayashita, Takashi
N1 - Funding Information:
This research was funded by a Grant-in-Aid for JSPS Fellows DC1 (grant no. 20J20891), a Grant-in-Aid for JSPS Fellows PD (grant no. 21J00709), a Grant-in-Aid for Scientific Research (C) (grant no. 18K05180), a Grant-in-Aid for Early Career Scientists (grant no. 18K14255), and a Grant-in-Aid for Scientific Research (B) (grant no. 20H02772) from the Japan Society for the Promotion of Science (JSPS), and was partly supported by The Precise Measurement Technology Promotion Foundation. This work was supported by a Sophia University Special Grant for Academic Research “Research in Priority Areas”.
Publisher Copyright:
© 2023 by the authors.
PY - 2023/2
Y1 - 2023/2
N2 - Antimicrobial-resistant (AMR) bacteria have become a critical global issue in recent years. The inefficacy of antimicrobial agents against AMR bacteria has led to increased difficulty in treating many infectious diseases. Analyses of the environmental distribution of bacteria are important for monitoring the AMR problem, and a rapid as well as viable pH- and temperature-independent bacterial separation method is required for collecting and concentrating bacteria from environmental samples. Thus, we aimed to develop a useful and selective bacterial separation method using a chemically synthesized nanoprobe. The metal-free benzoxaborole-based dendrimer probe BenzoB-PAMAM(+), which was synthesized from carboxy-benzoxaborole and a poly(amidoamine) (PAMAM) dendrimer, could help achieve Gram-positive bacterial separation by recognizing Gram-positive bacterial surfaces over a wide pH range, leading to the formation of large aggregations. The recognition site of benzoxaborole has a desirable high acidity and may therefore be responsible for the improved Gram-positive selectivity. The Gram-positive bacterial aggregation was then successfully collected by using a 10 μm membrane filter, with Gram-negative bacteria remaining in the filtrate solution. BenzoB-PAMAM(+) will thus be useful for application in biological analyses and could contribute to further investigations of bacterial distributions in environmental soil or water.
AB - Antimicrobial-resistant (AMR) bacteria have become a critical global issue in recent years. The inefficacy of antimicrobial agents against AMR bacteria has led to increased difficulty in treating many infectious diseases. Analyses of the environmental distribution of bacteria are important for monitoring the AMR problem, and a rapid as well as viable pH- and temperature-independent bacterial separation method is required for collecting and concentrating bacteria from environmental samples. Thus, we aimed to develop a useful and selective bacterial separation method using a chemically synthesized nanoprobe. The metal-free benzoxaborole-based dendrimer probe BenzoB-PAMAM(+), which was synthesized from carboxy-benzoxaborole and a poly(amidoamine) (PAMAM) dendrimer, could help achieve Gram-positive bacterial separation by recognizing Gram-positive bacterial surfaces over a wide pH range, leading to the formation of large aggregations. The recognition site of benzoxaborole has a desirable high acidity and may therefore be responsible for the improved Gram-positive selectivity. The Gram-positive bacterial aggregation was then successfully collected by using a 10 μm membrane filter, with Gram-negative bacteria remaining in the filtrate solution. BenzoB-PAMAM(+) will thus be useful for application in biological analyses and could contribute to further investigations of bacterial distributions in environmental soil or water.
KW - Gram-positive bacteria
KW - bacterial separation
KW - benzoxaborole
KW - dendrimer
KW - saccharide recognition
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U2 - 10.3390/molecules28041704
DO - 10.3390/molecules28041704
M3 - Article
C2 - 36838690
AN - SCOPUS:85149054027
SN - 1420-3049
VL - 28
JO - Molecules
JF - Molecules
IS - 4
M1 - 1704
ER -