• 제목/요약/키워드: biofilm inhibition

검색결과 91건 처리시간 0.025초

섬유상 담체를 이용한 영양염류 제거 및 조류 증식 억제에 관한 연구 (Efficiency of Nutritive Salts Removal and Algae Growth Inhibition Using a Fibrous Carrier)

  • 박신해;강대종;양경순;전수빈;오광중
    • 청정기술
    • /
    • 제21권4호
    • /
    • pp.257-264
    • /
    • 2015
  • 본 연구에서는 일반적인 물리·화학적 조류 증식 억제 방법의 문제점이 보완되어진 자연친화적인 생물학적 억제방법을 이용하고자 하였다. 섬유상 담체들의 생물막 형성 두께와 물리적 특성을 비교한 결과, 폴리에스터 담체가 가장 적절하였다. 이를 이용하여 부영양화 호소에서의 영양염류 제거와 조류증식 억제 효율을 분석하였다. 질소, 인 제거율은 14.59%, 6.36%, 그리고 조류증식 억제효율 비교를 위한 식물플랑크톤 성장 억제률은 77%로 영양염류와 식물플랑크톤 수치가 증가한 대조군에 비해서 높은 효율을 나타냈다. 따라서 본 연구에서는 폴리에스터 섬유상 담체를 적용하여 호소에서 자연친화적인 생물학적 처리가 가능할 것으로 판단된다.

Isovitexin, a Potential Candidate Inhibitor of Sortase A of Staphylococcus aureus USA300

  • Mu, Dan;Xiang, Hua;Dong, Haisi;Wang, Dacheng;Wang, Tiedong
    • Journal of Microbiology and Biotechnology
    • /
    • 제28권9호
    • /
    • pp.1426-1432
    • /
    • 2018
  • Staphylococcus aureus causes a broad variety of diseases. The spread of multidrug-resistant S. aureus highlights the need to develop new ways to combat S. aureus infections. Sortase A (SrtA) can anchor proteins containing LPXTG binding motifs to the bacteria surface and plays a key role in S. aureus infections, making it a promising antivirulence target. In the present study, we used a SrtA activity inhibition assay to discover that isovitexin, a Chinese herbal product, can inhibit SrtA activity with an $IC_{50}$ of $28.98{\mu}g/ml$. Using a fibrinogen-binding assay and a biofilm formation assay, we indirectly proved the SrtA inhibitory activity of isovitexin. Additionally, isovitexin treatment decreased the amount of staphylococcal protein A (SpA) on the surface of the cells. These data suggest that isovitexin has the potential to be an anti-infective drug against S. aureus via the inhibition of sortase activity.

Ginseng alleviates microbial infections of the respiratory tract: a review

  • Iqbal, Hamid;Rhee, Dong-kwon
    • Journal of Ginseng Research
    • /
    • 제44권2호
    • /
    • pp.194-204
    • /
    • 2020
  • The detrimental impact of air pollution as a result of frequent exposure to fine particles posed a global public health risk mainly to the pulmonary disorders in pediatric and geriatric population. Here, we reviewed the current literature regarding the role of ginseng and/or its components as antimicrobials, especially against pathogens that cause respiratory infections in animal and in vitro models. Some of the possible mechanisms for ginseng-mediated viral inhibition suggested are improvements in systemic and mucosa-specific antibody responses, serum hemagglutinin inhibition, lymphocyte proliferation, cell survival rate, and viral clearance in the lungs. In addition, ginseng reduces the expression levels of proinflammatory cytokines (IFN-γ, TNF-α, IL-2, IL-4, IL-5, IL-6, IL-8) and chemokines produced by airway epithelial cells and macrophages, thus preventing weight loss. In case of bacterial infections, ginseng acts by alleviating inflammatory cytokine production, increasing survival rates, and activating phagocytes and natural killer cells. In addition, ginseng inhibits biofilm formation and induces the dispersion and dissolution of mature biofilms. Most clinical trials revealed that ginseng, at various dosages, is a safe and effective method of seasonal prophylaxis, relieving the symptoms and reducing the risk and duration of colds and flu. Taken together, these findings support the efficacy of ginseng as a therapeutic and prophylactic agent for respiratory infections.

Burkholderia cepacia G4에 의한 트리클로로에틸렌의 공동대사적 분해에 미치는 성장기질의 영향 (Effects of Growth Substrates on Cometabolic Biodegradation of Trichloroethylene by Burkholderia cepacia G4)

  • 예병대;박성훈;이은열
    • KSBB Journal
    • /
    • 제15권5호
    • /
    • pp.474-481
    • /
    • 2000
  • The effects of growth substrates such as toluene and phenol on cometabolic biodegradation of trichloroethylene (TCE) by Burkholderia cepacia G4 were investigated. The dual effects of primary substrate on TCE biodegradation, stimulatory effects of toluene and phenol at low concentrations (0.5∼2 ppm & 0.1∼0.5 ppm, respectively) and a competitive inhibition at high concentration, were observed in batch experiments. These stimulatory effects of toluene and phenol were found to be due to the increments in the amount of reducing power like NADH which could be generated during the assimilation of toluene and phenol as the carbon and energy source. The efficiency of TCE biodegradation in trickling biofilm reactor (TBR) could be also enhanced up to the TCE removal efficiency of 58.1% by the supply of appropriate amounts of phenol (0.94∼4.7 ppm).

  • PDF

A Liquid Culture Bioassay System for the Detection of Quorum Sensing Signaling AHL Analogues

  • Kim, Young-Hee;Lee, Jae-Geun;Park, Sung-Hoon;Kim, Jung-Sun
    • 대한약학회:학술대회논문집
    • /
    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
    • /
    • pp.224.1-224.1
    • /
    • 2003
  • Recent studies have revealed that bacterial biofilm production by the gram-negative bacteria is regulated by the quorum sensing signaling molecules, AHLs (N-acyl homoserine lactones). This suggests that inhibiting the AHLs could enhance the effects of antibacterial agents. Halogenated furanones purified from the red algae Delisea pulchra have been known to decrease quorum sensing responses by competitive inhibition of the AHLs. (omitted)

  • PDF

Effect of Producing Different Phenazines on Bacterial Fitness and Biological Control in Pseudomonas chlororaphis 30-84

  • Yu, Jun Myoung;Wang, Dongping;Pierson, Leland S. III;Pierson, Elizabeth A.
    • The Plant Pathology Journal
    • /
    • 제34권1호
    • /
    • pp.44-58
    • /
    • 2018
  • Pseudomonas chlororaphis 30-84 is a biological control agent selected for its ability to suppress diseases caused by fungal pathogens. P. chlororaphis 30-84 produces three phenazines: phenazine-1-carboxylic acid (PCA), 2-hydroxy-phenazine-1-carboxylic acid (2OHPCA) and a small amount of 2-hydroxy-phenazine (2OHPHZ), and these are required for fungal pathogen inhibition and wheat rhizosphere competence. The two, 2-hydroxy derivatives are produced from PCA via the activity of a phenazine-modifying enzyme encoded by phzO. In addition to the seven biosynthetic genes responsible for the production of PCA, many other Pseudomonas strains possess one or more modifying genes, which encode enzymes that act independently or together to convert PCA into other phenazine derivatives. In order to understand the fitness effects of producing different phenazines, we constructed isogenic derivatives of P. chlororaphis 30-84 that differed only in the type of phenazines produced. Altering the type of phenazines produced by P. chlororaphis 30-84 enhanced the spectrum of fungal pathogens inhibited and altered the degree of take-all disease suppression. These strains also differed in their ability to promote extracellular DNA release, which may contribute to the observed differences in the amount of biofilm produced. All derivatives were equally important for survival over repeated plant/harvest cycles, indicating that the type of phenazines produced is less important for persistence in the wheat rhizosphere than whether or not cells produce phenazines. These findings provide a better understanding of the effects of different phenazines on functions important for biological control activity with implications for applications that rely on introduced or native phenazine producing populations.

Evaluation on Antimicrobial Activity of Psoraleae semen Extract Controlling the Growth of Gram-Positive Bacteria

  • Kim, Sejeong;Lee, Soomin;Lee, Heeyoung;Ha, Jimyeong;Lee, Jeeyeon;Choi, Yukyung;Oh, Hyemin;Hong, Joonbae;Yoon, Yohan;Choi, Kyoung-Hee
    • 한국축산식품학회지
    • /
    • 제37권4호
    • /
    • pp.502-510
    • /
    • 2017
  • This study investigated bacterial growth-inhibitory effect of 69 therapeutic herbal plants extracts on 9 bacterial strains using a disc diffusion assay. Especially, the antimicrobial activity of Psoraleae semen, which showed different activity on pathogenic Gram-positive and Gram-negative bacteria, was evaluated by MIC (minimal inhibition concentration) and biofilm formation assay. The effect of Psoraleae semen extract on bacterial cell membranes was examined by measurement of protein leakage (optical density at 280 nm) and scanning electron microscope (SEM). No clear zone was formed on discs containing Gram-negative bacteria, but Gram-positive bacteria exhibited clear zones. The MICs of Psoraleae semen extract were $8{\mu}g/mL$ for Streptococcus mutans, and $16{\mu}g/mL$ for Enterococci and Staphylococcus aureus. In addition, biofilm formation was inhibited at concentration $8-16{\mu}g/mL$. Protein leakage values and SEM images revealed that cell membranes of Gram-positive bacteria were impaired following exposure to the extract. Further, the extract inhibited the growth of Listeria monocytogenes in sausages. These results indicate that Psoraleae semen extract could be utilized as a natural antimicrobial agent against Gram-positive bacteria.

삼백초 추출물의 항치아우식 효과 (Anticariogenic Properties of the Extract of Saururus chinensis)

  • 이다홍;유현희;정수영;문해닮아;박기봉;조수민;전병훈;김인숙;유용욱
    • 동의생리병리학회지
    • /
    • 제21권3호
    • /
    • pp.647-651
    • /
    • 2007
  • It has been well established that S. mutans is the major etiological agent in dental caries, one of the most common oral diseases worldwide. The present study was designed to investigate the effect of Saururus chinensis (S. chinensis) ethanol extracts on the growth, acid production, biofilm formation, adhesion, and insoluble glucan synthesis of S. mutans. The ethanol extracts of S. chinensis showed concentration dependent inhibitory activity against the growth and acid production of S. mutans, and produced significant inhibition at the concentration of 0.025, 0.05, 0.1, 0.2 and 0.4 mg/ml compared to the control group. The extracts markedly inhibited S. mutans adherence to HA treated with saliva, and cell adherence was repressed by more than 80% at the concentration of 0.05 mg/ml and complete inhibition was observed at the concentration of 0.4 mg/ml. On the activity of glucosyltransferase which synthesizes water insoluble glucan form sucrose, ethanol extract of S. chinensis showed more than 10% inhibition over the concentration of 0.025 mg/ml. The synthesis of insoluble glucan was decreased in the presence of 0.025 ${\sim}$ 0.4 mg/ml of the ethanol extract of S. chinensis. Our research strongly suggested S. chinensis was a promising natural product for the prevention of dental caries.

세포벽 (1,3)-${\beta}$-D-Glucan Polymer 합성의 저해로 인한 황금(Scutellaria baicalensis)의 항바이오필름 활성 (Antibiofilm Activity of Scutellaria baicalensis through the Inhibition of Synthesis of the Cell Wall (1, 3)-${\beta}$-D-Glucan Polymer)

  • 김연희
    • 한국미생물·생명공학회지
    • /
    • 제41권1호
    • /
    • pp.88-95
    • /
    • 2013
  • Candida 바이오필름은 숙주조직과 의료기기의 표면에 자라는 자가-조직화된 미생물의 군락으로 전통적인 항진균제에 대한 저항성이 높게 나타난다. 황금(Scutellaria baicalensis)의 뿌리는 극동지방에서 의료용 목적으로 널리 사용되어 왔다. 본 연구의 목적은 10 C. albicans 임상 분리균주에 의해 형성된 바이오필름에 대한 황금의 수용성 추출물의 효과를 평가하고, 항바이오필름 활성에 대한 메커니즘을 알아보는 것이다. 바이오필름에 대한 효과는 XTT 환원분석법을 사용하였으며, 조사된 모든 균주에 대한 대사활성은 MIC에서 유의하게 감소($57.7{\pm}17.3$%)하였다. 황금추출물은 (1,3)-${\beta}$-D-글루칸 합성효소의 활성을 저해하였고 C. albicans의 형태에 대한 황금의 효과는 글루칸 합성의 억제로 인한 생장의 변화와 관련이 있었다: 대부분의 세포는 둥글고 팽창되었으며 세포벽이 진하게 염색되거나 파열되었다. 항캔디다 활성은 살진균성이었고, 황금은 C. albicans를 $G_0/G_1$기에 머물게 했다. 데이터는 황금이 목표가 되는 균류에 다중의 치명적인 효과를 내며, (1,3)-${\beta}$-D-글루칸 합성효소의 활성을 저해함을 통해 궁극적으로는 세포벽의 파열과 죽음에 이르게 한다는 것을 나타낸다. 따라서 황금은 바이오필름과 관련된 캔디다의 감염을 치료하고 제거하기 위한 항진균제 개발 후보 물질로서의 가능성을 가진다.

Porphyromonas gingivalis에 대한 오리나무 줄기 추출물의 항균활성 및 생물막 형성 억제 효과 (Antibacterial and Antibiofilm Activities of Alnus japonica Stem Extract against Porphyromonas gingivalis)

  • 김혜수;조수정
    • 생명과학회지
    • /
    • 제29권12호
    • /
    • pp.1386-1392
    • /
    • 2019
  • 본 연구에서는 천연물유래 구강건강소재로써 염료식물의 이용 가능성을 알아보기 위해 오리나무, 옻나무, 치자나무, 황칠나무, 황벽나무, 회화나무 줄기 추출물의 구강미생물에 대한 항균활성을 조사하였다. 6 종의 국내 자생 염료식물의 줄기에서 추출한 에탄올 추출물 중 오리나무 줄기 추출물(1 mg/disc)이 치주질환 원인균인 P. gingivalis KCTC5352에 대해 가장 우수한 항균활성을 나타내었다. 오리나무 줄기 추출물은 P. gingivalis KCTC5352에 대해 양성대조구로 사용한 chlorhexidine과 유사한 항균활성을 나타내었으며 P. gingivalis KCTC5352의 MIC는 0.4 mg/ml였고 MBC는 0.6 mg/ml였다. 오리나무 줄기 추출물이 0.2-2.0 mg/ml 농도로 처리된 배양액에서 P. gingivalis KCTC5352의 바이오필름 생성율과 세균 생육은 추출물의 농도가 증가할수록 저해되는 경향을 보였다. 또한 P. gingivalis KCTC5352의 superoxide dismutase (SOD)와 섬모에 대한 mRNA 발현도 추출물의 농도가 높아질수록 감소하는 것을 확인할 수 있었다. 이상의 결과를 종합하면 오리나무 줄기 추출물은 치주질환 원인균인 P. gingivalis KCTC5352에 대한 항균활성과 생물막 생성 억제능이 우수하기 때문에 천연물유래 구강건강소재로써 이용 가능성이 높을 것으로 판단된다.