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Phage-functionalized magnetic separation for rapid and selective detection of Escherichia coli
ID
Eigenfeld, Marco
(
Avtor
),
ID
Schneider, Benjamin
(
Avtor
),
ID
Kolb, Dagmar
(
Avtor
),
ID
Lisac, Ana
(
Avtor
),
ID
Podgornik, Aleš
(
Avtor
),
ID
Schwaminger, Sebastian P.
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(12,89 MB)
MD5: 4B23970DA20800A945D60D94200FAA62
URL - Izvorni URL, za dostop obiščite
https://pubs.acs.org/acsodf/article/11/25/37605/5170632/Phage-Functionalized-Magnetic-Separation-for-Rapid
Galerija slik
Izvleček
Selective bacterial preconcentration remains a key challenge for improving downstream molecular detection. Here, we report carboxymethyl-dextran (CMD) coated magnetic nanoparticle clusters functionalized with lytic T4 bacteriophages (phage@CMD) for selective capture of Escherichia coli. Iron-oxide particles were synthesized by coprecipitation and characterized by dynamic light scattering (DLS), Fourier transform infrared (FT-IR) spectroscopy, and electron microscopy, revealing CMD-stabilized nanoparticle clusters with a hydrodynamic diameter of approximately 181 nm with moderate dispersity (PDI = 0.267). T4 phages were immobilized via EDC/Sulfo-NHS chemistry, yielding a functional loading of ∼5.54 × 10$^{12}$ PFU-equivalent g$^{–1}$ (∼0.053 phage per particle). An empirical Langmuir-type analysis was used solely to estimate surface loading capacity. Phage-functionalized particles enabled magnetic capture of E. coli, resulting in experimentally determined separation efficiencies of ∼20–40%, verified by CFU depletion and PCR analysis of particle-associated fractions. Magnetic preconcentration improved the practical PCR input threshold compared to direct amplification of untreated suspensions. While the study represents a proof-of-concept in laboratory media, limitations including random phage orientation, partial loss of activity after immobilization, and lack of complex-matrix validation are discussed. These findings support the use of phage@CMD as a modular magnetic preconcentration platform for bacteria prior to nucleic-acid–based analysis.
Jezik:
Angleški jezik
Ključne besede:
bacteria
,
genetics
,
infectious diseases
,
nanoparticles
,
viruses
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
FKKT - Fakulteta za kemijo in kemijsko tehnologijo
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2026
Št. strani:
Str. 37605-37618
Številčenje:
Vol. 11, iss. 25
PID:
20.500.12556/RUL-188123
UDK:
602.3:578.347:620.3
ISSN pri članku:
2470-1343
DOI:
10.1021/acsomega.6c02406
COBISS.SI-ID:
286107395
Datum objave v RUL:
18.09.2026
Število ogledov:
68
Število prenosov:
13
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
ACS omega
Skrajšan naslov:
ACS omega
Založnik:
American Chemical Society
ISSN:
2470-1343
COBISS.SI-ID:
525873945
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
bakterije
,
genetika
,
nalezljive bolezni
,
nanodelci
,
virusi
Projekti
Financer:
DFG - German Research Foundation
Program financ.:
Deutsche Forschungsgemeinschaft
Številka projekta:
548540458
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