• 한국축산식품학회지
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• 제31권4호
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• pp.557-562
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• 2011

본 연구는 국내에서 유통되고 있는 액란의 냉장저장 중 미생물 및 이화학적 성상을 구명하기 위해 수행하였다. 본 실험에 사용된 액란은 살균 및 비살균 처리된 전란액, 난황액 및 난백액으로 여름철과 겨울철 생산 제품에 대해 각각 조사하였다. 냉장저장 중 세균수의 경우 여름철에 생산된 비살균 액란(전란액, 난황액 및 난백액)은 1,270-83,300 CFU/g 수준으로 겨울철에 생산된 비살균 액란의 0-4,330 CFU/g 에 비해 증가하는 것으로 나타났다. 살균 전란액과 살균 난황액에서는 저장기간 동안 액란생산 계절과 관계 없이 대장균군이 검출되지 않는 것으로 나타났다. 반면, 비살균 액란은 냉장저장 중 겨울철에 생산된 난백액에서만 대장균군이 검출되지 않는 것으로 나타났다. Salmonella는 살균 및 비살균 액란 모두에서 냉장저장 중 액란 생산 계절과 관계없이 검출되지 않았다. 그러나, 여름철에 생산된 비살균 전란액으로부터 Salmonella 의심균을 동정한 결과, Pseudomonas sp, Pseudomonas geezenne, Pseudomonas otitidis, Pseudomonas aeruginosa인 것으로 판명되었다. 액란의 냉장저장 중 pH 및 점도변화는 살균과 비살균 처리구간 뚜렷한 차이가 없는 것으로 나타났다. 이상의 결과를 종합해 볼 때 여름철에 비살균 액란 생산시 교차오염에 각별한 주의가 필요할 것으로 사료된다.

• Journal of Microbiology
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• 제42권3호
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• pp.216-222
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• 2004

In a previous paper, the ogdH gene that encodes 2-oxoglutarat dehydrogenase was isolated from Salmonella typhimurium. The catalytic N-terminal region in the enzyme was found to be very specific for the Salmonella species. Therefore, the aim of the present study was to detect S. typhimurium in food sources using primers designed for OGDH-l and OGDH-2 which were based on the salmonella-specific region of the ogdH gene. A simple polymerase chain reaction (PCR) detection method was developed to detect low numbers of S. typhimurium in a chicken meat microbial consortium. Using the ogdH-specific primers under stringent amplification conditions and for gene probe analysis, fewer than 100 colony-forming units (CFUs) were detectable when pure cultures were employed. When the PCR assay was run on S. typhimurium-contaminated meat contents, only the positive meat samples containing as few as 200 CFUs reacted to the assay. The method employed for sample processing is simple and it was determined to provide a sensitive means of detecting trace amounts of S. typhimurium-specific sequences in the presence of mixed meat microbial populations. When compared with six representative intestinal gram-negative bacterial strains in foods, including Vibrio parahaemolyticus, V. vulnificus, Enterobacter cloacae, E. coli O157:H7, Pseudomonas aeruginosa, and Proteus sp., S. typhimurium had a unique and distinct PCR product (796 bp). In conclusion, the two OGDH primers were found to be rapid and sensitive detectors of Salmonella spp for the PCR method.

• Journal of Microbiology and Biotechnology
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• 제32권12호
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• pp.1605-1614
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• 2022

The strains associated with foodborne Salmonella enterica Thompson outbreaks in Korea have not been identified. Therefore, we characterized S. Thompson strains isolated from chocolate cakes linked to foodborne outbreaks in Korea. A total of 56 strains were isolated from preserved cake products, products in the supply chain distribution, the manufacturer's apparatus, and egg white liquid products used for cream preparation. Subsequently, serological typing, pathogenic gene-targeted polymerase chain reaction (PCR), pulsed-field gel electrophoresis (PFGE), and whole-genome multi-locus sequence typing (wgMLST) were performed to characterize these isolates. The antigen formula of all isolates was 7:k:1,5, namely Salmonella enterica subsp. enterica Serovar Thompson. All 56 isolates harbored invA, his, hin, and stn, and were negative for sefA and spvC based on gene-targeted PCR analyses. Based on PFGE results, these isolates were classified into one group based on the same SP6X01.011 pattern with 100% similarity. We selected 19 strains based on the region and sample type, which were subjected to wgMLST. Although the examined strains showed 100% similarity, they were classified into seven clusters based on allelic differences. According to our findings, the cause of these outbreaks was chocolate cake manufactured with egg white liquid contaminated with the same Salmonella Thompson. Additionally, comparative analysis of wgMLST on domestic isolates of S. Thompson from the three outbreaks showed genetic similarities of over 99.6%. Based on the results, the PFGE and wgMLST combination can provide highly resolved phylogeny and reliable evidence during Salmonella outbreak investigations.

• 한국세라믹학회지
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• 제34권1호
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• pp.13-22
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• 1997

은 이온과 구리 이온을 동시에 함유하는 살균용 인산염계 수용성 유리를 용융법으로 제조하였다. 분말상의 유리 시편을 상온의 증류수에 넣어 조성과 시간에 따른 용해 특성을, bulk상 시편에 대해서는 용해 전.후의 표면변화를 각각 관찰하였고, 살균 효과 및 세포독성을 평가하였다. 은 이온:구리 이온=1:1인 조성에서 최대 용해량을 나타내었으며 용해거동은 초기부터 total dissolution이 지배적이었다. 시간의 경과에 따라 용해는 진행이 되지만, 표면에 생성되는 새로운 층은 관찰되지 않았다. Pseudomonas sp, e. coli, staphylococcus aureus, 및 salmonella균에 대한 살균 효과는 용해량의 증가에 따라 증가하여 우수한 살균효과를 나타내었다. L929 세포에 대한 독성 실험 결과, 은 이온의 농도가 10ppm이상에서만 독성을 나타내었다.

• 한국식품조리과학회지
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• 제21권1호
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• pp.53-63
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• 2005

4종류의 식품 위해 세균 Salmonella typhimurium, Listeria monocytogenes, Staphylococcus aureus, Esherichia coli과 김치 부패에 관여하는 곰팡이 Aspergillus sp. Penicillium sp.에 대하여 김치 재료에 의한 항균성을 조사하였다. Paper disc method로 측정한 생육저해환 결과 4 종류의 세균에 대하여 각 재료의 methanol 추출물들은 E. coli에 대해서 재료에 따라 약간의 차이는 있으나 약 20.00 mm에 가까운 항균성을 보이는 경향을 알 수 있었으며 생강과 양파는 다른 재료와 비교해볼 때 형성된 clear zone의 크기가 작은 경향을 확인할 수 있었다. 곰팡이에 대한 결과 Aspergillus sp.과 Penicillium sp.에 대하여 마늘 추출물이 가장 우수하였고, 생강 추출물과 무 추출물도 우수한 항균 작용을 나타내었다. S. typhimurium에 대하여 농도별 생육저해는 무, 양파 추출물이 균의 중식이 활발히 일어나는 대수중식기인 4$\~$12시간 사이에 생육을 억제하는 것으로 나타났고 고춧가루 추출물도 1,000 ppm의 농도에서 S. typhimurium의 생육을 크게 억제하는 것으로 나타났으며 L. monocytogenes의 생육에 미치는 영향은 S. typhimurium에 대한 결과 유사하였으며 paper disc로 조사한 생육 저해환의 결과와 일치하는 경향을 보였다. 반면 전체적으로 김치 재료 methanol 추출물은 S. aureus 생육 저해에 큰 영향을 미치지 못했으나 특별히 1,000 ppm 농도의 마늘 추출물이 S. aureus 생육에 있어서 유도기를 8시간까지 상당히 연장시켰다. Esherichia coli의 생육에 미치는 영향을 paper disc method로 측정한 생육저해환의 결과에서 대부분의 김치 재료 methanol 추출물이 우수한 항균성을 나타낸 것과 같이 농도별 생육 곡선을 측정한 결과에서도 미약하지만 모든 추출물에서 생육 억제 효과를 나타내었다. 최소저해농도(MIC)는 고춧가루 추출물이 L. monocytogenes에 대하여 500 $\mu$g/mL로 가장 낮은 값을 보였다.

• Journal of Microbiology
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• 제39권4호
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• pp.334-337
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• 2001

The degradative pathway of homoprotocatechuate (HPC) is the bacterial routhe wherby 3,4-dihydrox-yphenylactic acid is catabolized to pyruvate and succinate by a series of sequential reactions . The HPC is catalzed by homoprotocatechuate 2, 3-dioxygenase(HPC-2,3O) to from 5-carboxymethy1-2-hydroxy-muco semialdehyde. In this study, the hha D gene encoding. HPC, 2, 3O was Cloned from the chromo-somal DNA of Pseudomonas sp. DJ-12 and its nucleotide sequence was analyzed. The open reding frame of hpaD gene was found to be composed of 864 nucleotide pairs and to encode a poypetide with 287 amino acide residues. The deduced amino acid sequence of the HPC-2,3O from Pseudomonas. sp. DJ-12 exhibited 60~64% homology with those of the corresponding enzymes from E. coli. Salmonella enterica, and Klebsiella pneumoniae.

• 한국식품저장유통학회:학술대회논문집
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• 한국식품저장유통학회 2003년도 제23차 추계총회 및 국제학술심포지움
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• pp.201.1-201
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• 2003

생균제로서 가능성 있는 유산균의 선별을 위해 발효식품인 동치미로부터 분리된 균주들의 내산성, 내담즙성, 내췌장액성 및 유해균 억제능을 조사하였다. 특히 분리된 균종 중에서 FF-3가 인공위액과 담즙산에 대한 높은 내성을 나타내었을 뿐만 아니라, Salmonella sp. 과 Escherichia coli에 대하여 높은 항균 활성을 나타내었다. FF-3유래 박테리오신은 그람양성 및 음성 세균에서 넓은 항균 범위를 나타내었다. 본 연구에서 최종선별된 FF-3 균주를 16s rDNA sequence 동정한 결과 Lactobacillus sp.으로 확인되어 FF-3으로 명명하였다.

• 한국미생물·생명공학회지
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• 제47권3호
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• pp.459-464
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• 2019

This study aimed to identify and characterize the antimicrobial activity of prodigiosin produced by Serratia sp. $PDGS^{120915}$ isolated from stream water in Busan, Korea; the identification was performed using phonological, biochemical, and molecular techniques, including 16S rRNA sequence analysis. Prodigiosin from the bacterial culture was purified by high-performance liquid chromatography (HPLC), and its antimicrobial activity and minimum inhibitory concentrations (MICs) were evaluated against 10 intestinal pathogenic gram-positive and negative bacteria. The results revealed that the isolated prodigiosin exhibited high antimicrobial activity against Listeria monocytogenes, Bacillus cereus, Pseudomonas aeruginosa, Salmonella typhimurium, Staphylococcus aureus, and Vibrio parahaemolyticus; further, the isolated prodigiosin showed minimum inhibitory concentrations (MICs) between $3{\mu}g/ml$ and 30 mg/ml, but they were not active against Bacillus subtilis, Enterococcus faecalis, Klebsiella pneumonia, and Escherichia coli. In conclusion, prodigiosin isolated from Serratia sp. $PDGS^{120915}$ showed high antimicrobial activity against intestinal pathogenic bacteria and has potential applications in the development of new antimicrobial agents.

• KSBB Journal
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• 제26권1호
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• pp.62-68
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• 2011

To isolate Lactic acid bacteria for animals, we have screened from Kim-chi, swine intestine, swine feces, and dairy products by random selection and anti-viral, antipathogenic bacteria test. Among them, CLP-1 shown that inhibitory effect against rotavirus, porcine epidemic diarrhea (PED) virus, Salmonella sp, and E.coli. By examining biological property, API-ZYM and identified Lactobacillus plantarum by 16S rDNAgene sequence. CLP-1 determined resistance to low pH and bile salt. Futhermore, the cell body of CLP-1 adhered to the intestinal epithelium tissue of swine and Caco-2 cell. CLP-1 was examined on cell immune system modulating activity in vitro. The whole cell and cell culture supernatant was increasing of interferon-${\beta}$ activity. And then, CLP-1 increased prevention effect by Salmonella enteritidis infection in SPF chickens. And we determined similar result in pigs.

• 한국식품영양과학회지
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• 제24권3호
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• pp.440-445
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• 1995

The antimutagenic effects of juices from green pepper(GP), red pepper leaf(RPL), red pepper(RP) and sweet pepper(SP) were examined by the Ames method using Salmonella typhimurium TA100. The juice supernatants of GP, RPL and RP showed antimutagenic activities against afltoxin B1(AFB1) in Salmonella typhimurium TA 100. The juice supermatants of GP and RPL also exhibited the inhibitory effects(p<0.05) to the mutagenicities induced by N-methyl-N'-nitro-N-nitrosoguanidine(MNNG) and 4-nitro-quinoline-1-oxide(4-NQO). The juice of RP showed antimutagenic activities against indirect mutagen of AFB1, however, the activity was reduced at higher concentration(5.0%), furthermore, as the adding concentration of sample increased to 5.0%, it exhibited slight comutagenicith on direct mutagen of MNNG. Theantimutagenic activities of GP and RPL juices were reduced significantly after heating at 100℃ for 20min, supposing that the antimutagenic compound(s) in the juices were heat labile.