• 산업기술연구
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• 제29권A호
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• pp.169-176
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• 2009

The gene encoding endoxylanase (xylS) was isolated from a genomic library of Bacillus licheniformis NBL420. Two positive clones, which harbor 1.5 kb and 0.8 kb inserts respectively, were screened on RBB dyed-xylan plates and the recombinant plasmids were named as pBX3 and pBX5. The nucleotide sequencings of two inserts revealed the existence of common 639 bp of open reading frame which encode 232 amino acids. The xylS gene was successfully subcloned into pET22b(+) vector and overexpressed. Enzymatic properties including optimum pH, optimum temp, thermostability and pH stability were investigated. Activity staining of XylS was identical with that of original Bacillus licheniformis NBL420.

• 미생물학회지
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• 제54권2호
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• pp.169-170
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• 2018

Clindamycin 내성 Bacillus licheniformis 14ADL4 균주는 된장으로부터 분리되었다. 14ADL4 균주의 유전체분석 결과, GC 함량 45.86%, 약 4.3 Mb 크기의 염색체가 확인되었고, 유전체 상의 lmrA와 lmrB 추정 유전자가 clindamycin 내성에 관여할 것으로 예상된다.

• Environmental Engineering Research
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• 제23권3호
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• pp.258-264
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• 2018

The objectives of this research were to 1) isolate and identify thermophilic bacteria for food waste treatment; 2) investigate the capability of food waste treatment using Bacillus species; and 3) develop air-dried Bacillus starters for food waste treatment. Five Bacillus species were isolated from food wastes and identified as Bacillus licheniformis (B. licheniformis) G1, Bacillus circulans C2, Bacillus subtilis (B. subtilis) E1, Bacillus vanillea F1, and Bacillus atrophaeus G2 based on 16S rDNA sequencing. Each identified Bacillus and the mixture of Bacillus species were cultivated in the standard food waste at $45^{\circ}C$ for 8 d. Changes in cell count, solid contents, and pH of the food waste were monitored during cultivation. Air-dried Bacillus cell powders were prepared using wheat flour and lactomil as excipients, and the cell count and survival rate were determined. The cell count of B. licheniformis G1 exhibited the highest number among the tested Bacillus (${\sim}10^8CFU/mL$). The greatest reduction in solid contents of food waste was achieved by B. subtilis E1 (22.6%). The mixture of B. licheniformis G1 and B. subtilis E1 exhibited a synergistic effect on the reduction of solid contents. Lactomil was determined as better excipient than wheat flour based on the greatest survival rate of 95%.

• Applied Biological Chemistry
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• 제40권3호
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• pp.173-177
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• 1997

Bacillus licheniformis 9945a는 액체배양시 ${\gamma}-poly(glutamic\;acid)$를 균체외로 분비하며, 한천배지에 고체 배양시는 점액질의 군락을 나타낸다. 점액질의 Bacillus속 세균의 형질전환은 그리 순하지 않은 것으로 알려져 있으며, B. licheniformis에서의 trasposon Tn10의 활성여부도 알려져 있지 않다. 그래서 점액질을 분비하지 않는, B. licheniformis의 자연발생적 변이주를 우선 분리하였다. Mini-Tn10을 함유한 plasmid pHV1248을 protoplast transformation법에 준해서 이 변이주에 도입하여 형질전환체를 분리하였다. pHV1248을 함유한 형질전환체를 점액성의 야생형질로 복귀시킨 후에, 가열처리함으로써 무작위 돌연변이를 유도하였다. Arginine, lysine 또는 tryptohan을 생육인자로 요구하는 돌연변이주들이 replica plating method에 의해서 분리되었고, 이 들 영양요구성 변이주는 mini-Tn10이 염색체 DNA상에 삽입됨으로써 생겨났음이 Southern blotting과 DNA-DNA 혼성화 실험으로 증명되었다. 이러한 pHV1248을 이용한 형질전환 및 돌연변이 유도방법은 Bacillus licheniformis 9945a의 다양한 변이체를 얻는데 유용할 것이다.

• 미생물학회지
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• 제54권4호
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• pp.453-455
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• 2018

된장으로부터 콩발효 종균후보 Bacillus licheniformis 0DA23-1가 분리되었다. 0DA23-1 균주는 GC 함량 45.96%, 약 4.4 Mb 크기의 단일 chromosome을 보유하고 있었고, 식중독균 Bacillus cereus 및 Staphylococcus aureus가 보유한 위해성 유전자는 유전체로부터 확인되지 않았다. 또한, 8종의 항생물질(chloramphenicol, clindamycin, erythromycin, gentamicin, kanamycin, streptomycin, tetracycline, vancomycin) 저항성 및 혈청분해 활성, 바이오필름 생성 관련 유전자도 확인되지 않았다.

• KSBB Journal
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• 제20권5호
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• pp.359-362
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• 2005

Bacillus licheniformis는 장내 균총을 개선하는데 유용한 물질이다. 본 연구의 목포는 B. licheniformis의 낮은 pH (pH 2, 3, 4, 6, 7), 인공 담즙산, 높은 농도의 염 (0. 5, 10, 20, $30\%$) 그리고 에탄올 (0, 4, 3, 16, $32\%$)에 대한 안정성을 확인하려고 한다. B. licheniformis는 pH 3, 4, 6, 7에서 안정적인 생존율을 보였다. B. llicheniformis의 담즙 내에서의 최종 생존율은 $25\%$ 이하로 확인되었다. 높은 농도의 염에서는 B. licheniformis는 $10\%$의 염에서 최적 생존율을 보였다. licheniformis의 에탄올이 포함되지 않은 것에 비해 에탄올이 4, 8, 16, $32\%$ 포함된 것에서 $95\%$ 이상의 생존율을 보였다. 그러므로 B. licheniformis가 pH 3, 4, 6, 7, 높은 농도의 염, 에탄올에서 안정하나 pH 2와 담즙산에서 불안정하다는 것을 확인할 수 있었다.

• Journal of Microbiology and Biotechnology
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• 제5권1호
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• pp.22-25
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• 1995

Bacillus licheniformis SSA3 can produce a dark-brown antimutagenic pigment. The optimal conditions for production of this pigment are reached at 0.1% tyrosine, in pH 6-8, within 7-9 days, at $30^{\circ}C$, and in aerobic condition. We cloned a DNA fragment involved in pigment synthesis from Bacillus licheniformis SSA3 using a mutant strain. The cloned DNA was 7kb in size, which can produce the same pigment even in E. coli.

• Tuberculosis and Respiratory Diseases
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• 제57권6호
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• pp.553-556
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• 2004

Bacillus종은 그람양성 간균으로 포자를 형성하며 주변 환경 어디에나 존재하여 임상 가검물에서 분리되는 경우 대부분 오염균으로 생각된다. B. licheniformis에 의한 감염증인 경우 외상, 면역저하, 주사약물남용과 연관성을 가지며, 적절한 항생제 사용과 카테타 제거나 수술적 국소조직 제거에 의해 잘 치유되는 특징이 있다. 그러나 위험인자가 없는 상태에서도 B. licheniformis 균혈증은 생길 수 있으며 본 증례에서도 58세의 위험인자가 없던 여자에서 기관지경 후에 B. licheniformis 균혈증이 발생하였고 다른 증례들처럼 경험적 항생제 치료 후에 합병증 없이 치유되었다.

• Journal of Microbiology and Biotechnology
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• 제28권12호
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• pp.1992-1998
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• 2018

In 2015, Bacillus paralicheniformis was separated from B. licheniformis on the basis of phylogenomic and phylogenetic studies, and urease activity was reported as a phenotypic property that differentiates between the two species. Subsequently, we have found that the urease activity of B. paralicheniformis is strain-specific, and does not reliably discriminate between species, as strains having the same urease gene cluster were identified in B. licheniformis and B. sonorensis, the closest relatives of B. paralicheniformis. We developed a multilocus sequence typing scheme using eight housekeeping genes, adk, ccpA, glpF, gmk, ilvD, pur, spo0A, and tpi to clearly identify B. paralicheniformis from closely related Bacillus species and to find a molecular marker for the rapid identification of B. paralicheniformis. The scheme differentiated 33 B. paralicheniformis strains from 90 strains formerly identified as B. licheniformis. Among the eight housekeeping genes, spo0A possesses appropriate polymorphic sites for the design of a B. paralichenofomis-specific PCR primer set. The primer set designed in this study perfectly separated B. paralicheniformis from B. licheniformis and B. sonorensis.

• 한국축산시설환경학회지
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• 제21권3호
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• pp.83-92
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• 2015

An attempt to produce more pigs in limited spaces inevitably generalized concentrated feeding operation (CFO). As concentrated pig production practice expanded, concerns on environmental issues grow concurrently. Since odor is the concerned most among those, we attempted to develop means to tackle odor emission from livestock operations. Previously, we excavated few microorganisms from pig manure and, one of them, Bacillus licheniformis was particularly useful to handle odor problem. In this study, we conducted our investigation to further characterize Bacillus licheniformis. Strain identification was conducted using Vitek 2 compact, and the optimal temperature and pH conditions to growth B. licheniformis were searched for by analyzing turbidity on O.D 600 nm. Results of this study can be summarized as these, (1) it was re-verified that the bacterial strain that purified from pig manure was, in fact, Bacillus licheniformis, (2) the bacterial growth was highest when the temperature was kept at $30^{\circ}C$, also (3) growth rate was dependent on media pH as it was high at neutral (6, 7 and 8) but dropped when it was diverged from neutral (4, 5, 9 and 10), and (4) regarding ammonia removal efficiency, B. licheniformis recorded 64% effectiveness after 48 h incubation and reached its highest (80%) at 72 h.