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Research Article
Transcriptomic insights into the effects of sublethal exposure to endolysin LNT113 on Escherichia coli
Heymin Song, Nanjoo Park, Eunsuk Kim, Seowon Jang, Sunghoon Kim, Jeongik Cho, Hyunjin Yoon
J. Microbiol. 2026;64(7):e2605009.   Published online July 31, 2026
DOI: https://doi.org/10.71150/jm.2605009
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AbstractAbstract PDFSupplementary Material

The global rise of multidrug-resistant bacteria poses a critical threat to public health, and bacteriophage-derived endolysins have emerged as promising alternatives to conventional antibiotics. The engineered endolysin LNT113, derived from the Escherichia coli phage PBEC131 endolysin EC340, exhibits potent lytic activity against Gram-negative bacteria. This study investigated the transcriptomic responses of E. coli to sublethal LNT113 stress and identified genetic determinants required for bacterial adaptation to endolysin-induced stress. Transcriptomic analysis identified 552 differentially expressed genes (DEGs) following sublethal LNT113 exposure. Thirteen DEGs associated with stress response and envelope maintenance were individually deleted to generate thirteen mutant strains and to functionally evaluate their roles in bacterial stress tolerance. Among these, the ΔfabB and Δ(prmByfcL) mutants exhibited significantly reduced survival under sublethal LNT113 exposure, indicating increased susceptibility to the endolysin. Regarding the prmByfcL operon, individual genes were deleted to determine the gene critical for bacterial tolerance. Deletion of aroC and mepA rendered E. coli more susceptible to LNT113. Furthermore, 1-N-phenylnaphthylamine uptake assays demonstrated increased membrane permeability in the ΔfabB, ΔaroC, and ΔmepA mutants. Complementation with pWSK129::fabB, pWSK129::aroC, and pWSK129::mepA restored membrane integrity in the respective mutant strains. These findings suggest that fabB-mediated unsaturated fatty acid biosynthesis and mepA-dependent peptidoglycan remodeling are critical for maintaining envelope integrity under endolysin stress, whereas aroC may indirectly support bacterial tolerance to LNT113 via metabolic adaptation. This study provides insights into bacterial responses to LNT113 and offers a foundation for optimizing endolysin-based therapeutic strategies.

Article
Rapid determination of carbapenem resistance by low-cost colorimetric methods: Propidium Iodide and alamar blue staining
Jiyoon Choi , Jiwon Baek , Daehyuk Kweon , Kwan Soo Ko , Hyunjin Yoon
J. Microbiol. 2020;58(5):415-421.   Published online March 28, 2020
DOI: https://doi.org/10.1007/s12275-020-9549-x
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  • 5 Web of Science
  • 5 Crossref
AbstractAbstract PDF
Carbapenems are a class of β-lactam antibiotics with a broad antimicrobial activity spectrum. Owing to their sturdy structures resistant to most β-lactamases, they have been regarded as one of the last-resort antibiotics for combating multidrugresistant bacterial infections. However, the emergence of carbapenem resistance increases predominantly in nosocomial pathogens. To prevent spread of carbapenem resistance in early stages, it is imperative to develop rapid diagnostic tests that will substantially reduce the time and cost in determining carbapenem resistance. Thus, we devised a staining-based diagnostic method applicable to three different Gram-negative pathogens of Acinetobacter baumannii, Escherichia coli, and Klebsiella pneumoniae, all with the high potential to develop carbapenem resistance. Regardless of the resistance mechanisms presented by bacterial species and strains, double staining with propidium iodide (PI) and alamar blue (AB) identified resistant bacteria with an average sensitivity of 95.35%, 7 h after imipenem treatments in 343 clinical isolates. Among the three species tested, A. baumannii showed the highest diagnostic sensitivity of 98.46%. The PI and ABmediated staining method could be a promising diagnostic
method
with high-throughput efficacy and low cost.

Citations

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  • Rapid Determination of Antibiotic Resistance in Klebsiella pneumoniae by a Novel Antibiotic Susceptibility Testing Method Using SYBR Green I and Propidium Iodide Double Staining
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    Analytical Chemistry.2021; 93(17): 6784.     CrossRef
Research Support, Non-U.S. Gov't
ppGpp-Mediated Stationary Phase Induction of the Genes Encoded by Horizontally Acquired Pathogenicity Islands and cob/pdu Locus in Salmonella enterica serovar Typhimurium
Miryoung Song , Hyun-Ju Kim , Sangryeol Ryu , Hyunjin Yoon , Jiae Yun , Hyon E. Choy
J. Microbiol. 2010;48(1):89-95.   Published online March 11, 2010
DOI: https://doi.org/10.1007/s12275-009-0179-6
  • 640 View
  • 1 Download
  • 12 Crossref
AbstractAbstract PDF
Salmonella enterica is highly diverse in terms of genome structure, which is at least partly due to the horizontal transfer of genetic elements from various sources. In this study, we examined the expression profiles of such genes in Salmonella Pathogenicity Islands (SPIs) and the cob/pdu locus, horizontally acquired large DNA segments, during growth under standard growth conditions. Transcripts from exponentially growing and early stationary phase Salmonellae were compared using various methods including cDNA microarray analysis. Nearly all genes encoded by SPIs and the cob/pdu locus were induced at the onset of the stationary phase in a stringent molecule ppGpp-dependent but stationary phase σ, σ38-independent manner. Although, it has been suggested that ppGpp acts in concert with DksA, we found the stationary phase induction of those SPI genes was not DksA dependent. It is suggested that ppGpp stimulates the expression of these stress-inducible genes encoded by horizontally acquired DNA, by itself or in concert with DksA.

Citations

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    Science Advances.2026;[Epub]     CrossRef
  • Intrinsic antimicrobial resistance: Molecular biomaterials to combat microbial biofilms and bacterial persisters
    Swagatam Barman, Leman Buzoglu Kurnaz, Ryan Leighton, Md Waliullah Hossain, Alan W. Decho, Chuanbing Tang
    Biomaterials.2024; 311: 122690.     CrossRef
  • Innovative Approaches of Engineering Tumor-Targeting Bacteria with Different Therapeutic Payloads to Fight Cancer: A Smart Strategy of Disease Management
    Khaled S Allemailem
    International Journal of Nanomedicine.2021; Volume 16: 8159.     CrossRef
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    Fereshteh Badie, Maryam Ghandali, Seyed Alireza Tabatabaei, Mahmood Safari, Ahmad Khorshidi, Mohammad Shayestehpour, Maryam Mahjoubin-Tehran, Korosh Morshedi, Amin Jalili, Vida Tajiknia, Michael R. Hamblin, Hamed Mirzaei
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    Daejin Lim, Kwang Soo Kim, Hyun-Ju Kim, Kyong-Cheol Ko, Jae Jun Song, Jong Hyun Choi, Minsang Shin, Jung-Joon Min, Jae-Ho Jeong, Hyon E. Choy
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    Vinoy K. Ramachandran, Neil Shearer, Arthur Thompson, Muna Anjum
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  • A Novel Balanced-Lethal Host-Vector System Based on glmS
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  • Engineering and Visualization of Bacteria for Targeting Infarcted Myocardium
    Uyenchi N Le, Hyung-Seok Kim, Jin-Sook Kwon, Mi Yeon Kim, Vu H Nguyen, Sheng Nan Jiang, Byeong-Il Lee, Yeongjin Hong, Myung Geun Shin, Joon Haeng Rhee, Hee-Seung Bom, Youngkeun Ahn, Sanjiv S Gambhir, Hyon E Choy, Jung-Joon Min
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