• 제목/요약/키워드: surfactin

검색결과 60건 처리시간 0.021초

청국장 발효 균주인 Bacillus subtilis 028-1의 항생물질 생산과 특성 (Characterization and Production of Antibiotic by Bacillus subtilis 028-1, a Chungkookjang Fermenting Strain)

  • 안경준
    • 미생물학회지
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    • 제45권2호
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    • pp.185-192
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    • 2009
  • Bacillus subtilis 028-1 균주는 청국장 발효에 사용하는 균주로 Staphylococcus sp. LS2 뿐만 아니라 여러 yeast 균주의 생장을 억제하는 항생물질을 생산하며, soybean meal 2%와 maltose와 같은 이당류를 1% 첨가하여 15~18시간 진탕 배양하였을 때 최대의 항생물질 생산을 보였으며 배지의 pH는 6.5 이하였다. 항생물질의 활성은 약염기성 조건에서 극대화되었으며, $100^{\circ}C$에서 20분간 가열하여도 활성은 크게 감소하지 않았고, 실온 보관 시 한 달 이상 효과가 지속되며 chymotrypsin과 papain 같은 단백질 분해효소 처리에 의해 서서히 활성이 줄어들었다. 투석에 의해 항생물질의 분자량을 측정한 결과 1,000에서 500 dalton 사이인 것으로 나타났으며 항미생물 효과는 있으나 fibrin 분해 능력이 없으므로 surfactin이 아닌 iturin 계열의 peptide성 항생물질로 보인다.

Exploring the Potentiality of Novel Rhizospheric Bacterial Strains against the Rice Blast Fungus Magnaporthe oryzae

  • Amruta, Narayanappa;Kumar, M.K. Prasanna;Puneeth, M.E.;Sarika, Gowdiperu;Kandikattu, Hemanth Kumar;Vishwanath, K.;Narayanaswamy, Sonnappa
    • The Plant Pathology Journal
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    • 제34권2호
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    • pp.126-138
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    • 2018
  • Rice blast caused by Magnaporthe oryzae is a major disease. In the present study, we aimed to identify and evaluate the novel bacterial isolates from rice rhizosphere for biocontrol of M. oryzae pathogen. Sixty bacterial strains from the rice plant's rhizosphere were tested for their biocontrol activity against M. oryzae under in vitro and in vivo. Among them, B. amyloliquefaciens had significant high activity against the pathogen. The least disease severity and highest germination were recorded in seeds treated with B. amyloliquefaciens UASBR9 (0.96 and 98.00%) compared to untreated control (3.43 and 95.00%, respectively) under in vivo condition. These isolates had high activity of enzymes in relation to growth promoting activity upon challenge inoculation of the pathogen. The potential strains were identified based on 16S rRNA gene sequencing and dominance of these particular genes were associated in Bacillus strains. These strains were also confirmed for the presence of antimicrobial peptide biosynthetic genes viz., srfAA (surfactin), fenD (fengycin), spaS (subtilin), and ituC (iturin) related to secondary metabolite production (e.g., AMPs). Overall, the results suggested that application of potential bacterial strains like B. amyloliquefaciens UASBR9 not only helps in control of the biological suppression of one of the most devastating rice pathogens, M. grisea but also increases plant growth along with a reduction in application of toxic chemical pesticides.

식물생육촉진, 항균 및 저항성 유도 효과를 나타내는 내생세균 Bacillus velezensis YC7010의 유전체 염기서열 (Complete genome sequence of Bacillus velezensis YC7010, an endophytic bacterium with plant growth promoting, antimicrobial and systemic resistance inducing activities in rice)

  • 라시드엠디하룬;황정현;정영륜
    • 미생물학회지
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    • 제53권4호
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    • pp.329-331
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    • 2017
  • 식물 내생 세균인 Bacillus velezensis YC7010은 벼의 병원성 세균과 곰팡이에 대해 전신유도저항성을 일으키며, 식물생육촉진 및 항생작용의 특징을 가지고 있다. 대한민국 진주지역 벼의 근권에서 분리된 B. velezensis YC7010의 유전체는 3,790개의 단백질-암호화 유전자(86 tRNAs와 27 rRNA 유전자)로 구성되어 있으며, 3,975,683 염기쌍의 환상 염색체이다. 유전체 분석을 통해 식물의 발달과 생육을 촉진하는 휘발성 화합물, 식물호르몬 생산, surfactin, plipapastatin, bacillibactin, bacillaene 같은 활성 화합물의 생합성, 식물 내부정착 및 군집화와 관련된 유전자들이 유전체에 존재하는 것을 확인하였다

Screening Plant Growth-Promoting Bacteria with Antimicrobial Properties for Upland Rice

  • Khammool Khamsuk;Bernard Dell;Wasu Pathom-aree;Wanwarang Pathaichindachote;Nungruthai Suphrom;Nareeluk Nakaew;Juangjun Jumpathong
    • Journal of Microbiology and Biotechnology
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    • 제34권5호
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    • pp.1029-1039
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    • 2024
  • This study explores beneficial bacteria isolated from the roots and rhizosphere soil of Khao Rai Leum Pua Phetchabun rice plants. A total of 315 bacterial isolates (KK001 to KK315) were obtained. Plant growth-promoting traits (phosphate solubilization and indole-3-acetic acid (IAA) production), and antimicrobial activity against three rice pathogens (Curvularia lunata NUF001, Bipolaris oryzae 2464, and Xanthomonas oryzae pv. oryzae) were assessed. KK074 was the most prolific in IAA production, generating 362.6 ± 28.0 ㎍/ml, and KK007 excelled in tricalcium phosphate solubilization, achieving 714.2 ± 12.1 ㎍/ml. In antimicrobial assays using the dual culture method, KK024 and KK281 exhibited strong inhibitory activity against C. lunata, and KK269 was particularly effective against B. oryzae. In the evaluation of antimicrobial metabolite production, KK281 and KK288 exhibited strong antifungal activities in cell-free supernatants. Given the superior performance of KK281, taxonomically identified as Bacillus sp. KK281, it was investigated further. Lipopeptide extracts from KK281 had significant antimicrobial activity against C. lunata and a minimum inhibitory concentration (MIC) of 3.1 mg/ml against X. oryzae pv. oryzae. LC-ESI-MS/MS analysis revealed the presence of surfactin in the lipopeptide extract. The crude extract was non-cytotoxic to the L-929 cell line at tested concentrations. In conclusion, the in vitro plant growth-promoting and disease-controlling attributes of Bacillus sp. KK281 make it a strong candidate for field evaluation to boost plant growth and manage disease in upland rice.

인삼모잘록병원균에 항균활성을 갖는 Bacillus 균의 분리 및 특성조사 (Isolation and Characterization of Bacillus Species Having Antifungal Activity Against Pathogens of Ginseng Damping Off)

  • 박경훈;박홍우;이성우;이승호;명경선;이상엽;송재경;김영탁;박경수;김영옥
    • 농약과학회지
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    • 제20권4호
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    • pp.380-387
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    • 2016
  • 인삼 모잘록병을 일으키는 병원균의 생물적 방제제 개발을 위하여 인삼 근권 토양으로 부터 500종의 미생물을 분리하였다. 인삼모잘록병원균을 대상으로 항균활성을 검정한 결과, 항균활성이 우수한 균주 3종을 선발하였다. 선발한 균주를 대상으로 항생물질과 세포벽분해효소 생성능력을 조사하였으며, fengycin, bacillomycin D, surfactin, iturin A와 zwittermicin A와 같은 리포펩타이드 생합성 유전자 유무를 조사하였다. ES1과 ES3 균주에서 iturin A와 surfactin 생합성 유전자를 확인하였으며, 세포벽 분해효소 생성능을 확인한 결과 선발한 모든 균주에서 cellulase, pectate lyase, protease를 생성하였다. 16S rRNA 염기서열 분석에 기반하여 계통도를 분석한 결과 ES1 균주와 ES3 균주는 Bacillus methylotrophucus로 확인되었으며, ES2는 B. amyloliquefaciens로 동정되었다. 포장실험 결과 ES1, ES2, ES3 처리구에서 각각 32.4%, 46.8%, 36.7%의 방제효과를 보였다. 이러한 결과로부터 항균활성과 세포벽 분해 효소 생성능이 우수한 길항균주를 선발하였으며, 향후 포장실험과 제형화 개발 등을 통해 인삼모잘록병 방제를 위한 생물적 방제제로 활용할 수 있을 것으로 기대된다.

Postharvest Biological Control of Colletotrichum acutatum on Apple by Bacillus subtilis HM1 and the Structural Identification of Antagonists

  • Kim, Hae-Min;Lee, Kui-Jae;Chae, Jong-Chan
    • Journal of Microbiology and Biotechnology
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    • 제25권11호
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    • pp.1954-1959
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    • 2015
  • Bacillus subtilis HM1 was isolated from the rhizosphere region of halophytes for its antifungal activity against Colletotrichum acutatum, the causative agent of anthracnose. Treatment of postharvest apples with the cell culture or with a cell-free culture supernatant reduced disease severity 80.7% and 69.4%, respectively. Both treatments also exhibited antifungal activity against various phytopathogenic fungi in vitro. The antifungal substances were purified and analyzed by acid precipitation, gel filtration, high-performance liquid chromatography, and matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). Three compounds were identified as fengycin, iturin, and surfactin. The MALDI-TOF/TOF mass spectrum revealed the presence of cyclized fengycin homologs A and B, which were distinguishable on the basis of the presence of either alanine or valine, respectively, at position 6 of the peptide sequence. In addition, the cyclized structure of fengycin was shown to play a critical role in antifungal activity.

Bacillus subtilis KL-57로부터 생산되는 생체계면활성제 합성 유전자 클로닝 (Cloning of Biosurfactant-Producing Gene from Bacillus subtilis KL-57)

  • 강상모;이병옥;이철수
    • 한국미생물·생명공학회지
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    • 제22권6호
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    • pp.593-598
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    • 1994
  • A bacterium KL-57 which exhibited biosurfactant activity was isolated. This bacterium was identified as Bacillus subtilis. The biosurfactant-producing gene of B. subtilis KL-57 was cloned into R subtilis MI113 by using plasmid pTB523. The plasmid DNA from the clone was found to carry a 18 kb PstI insert. The biosurfactant-producing gene was cleaved into 4 fragments by SmaI, 3 fragments by PvulI or EcoRl, 4 fragments by PvulI and EcoRI double digestion, 5 fragments by AccI, and 2 fragments by KpnI, HindIII or BamHI. By subcloning the 18 kb Pstl insert, a 2.3 kb EcoRl fragment conferred the biosurfactant producing activity on B. subtilis cells. The 2.3 kb had one HindIII cleave site. But Two fragments, which corresponds HindIII/EcoRl termini, exhibited no biosurfactant activity.

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Characterization of an Antibiotic Produced by Bacillus subtilis JW-1 that Suppresses Ralstonia solanacearum

  • Kwon, Jae Won;Kim, Shin Duk
    • Journal of Microbiology and Biotechnology
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    • 제24권1호
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    • pp.13-18
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    • 2014
  • Bacillus subtilis JW-1 was isolated from rhizosphere soil as a potential biocontrol agent of bacterial wilt caused by Ralstonia solanacearum. Seed treatment followed by a soil drench application with this strain resulted in >80% reduction in bacterial wilt disease compared with that in the untreated control under greenhouse conditions. The antibacterial compound produced by strain JW-1 was purified by bioactivity-guided fractionation. Based on mass spectroscopy and nuclear magnetic resonance spectral data ($^1H$, $^{13}C$, $^1H-^1H$ correlation spectroscopies, rotating frame nuclear Overhauser effect spectroscopy, and heteronuclear multiple-bond correlation spectroscopy), the structure of this compound was elucidated as a cyclic lipopeptide composed of a heptapeptide (Gln-Leu-Leu-Val-Asp-Leu-Leu) bonded to a ${\beta}$-hydroxy-iso-hexadecanoic acid arranged in a lactone ring system.