• 제목/요약/키워드: European honey

검색결과 7건 처리시간 0.019초

Detection of Korean Native Honey and European Honey by Using Duplex Polymerase Chain Reaction and Immunochromatographic Assay

  • Kim, Chang-Kyu;Lee, Deug-Chan;Choi, Suk-Ho
    • 한국축산식품학회지
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    • 제37권4호
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    • pp.599-605
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    • 2017
  • Korean native honey (KNH) is much more expensive than European honey (EH) in Korea, because KNH is a favored honey which is produced less than EH. Food fraud of KNH has drawn attention of the government office concerned, which is in need of a method to differentiate between KNH and EH which are produced by the Asiatic honeybee, Apis cerana and the European honeybee, Apis mellifera, respectively. A method to discriminate KNH and EH was established by using duplex polymerase chain reaction (PCR) in this study. Immunochromatographic assay (IC) was examined to analyze the duplex PCR product. The DNA sequences of primers for the duplex PCR were determined by comparing cytochrome C oxidase genes of the two honey bee species. Chelex resin method was more efficient in extracting genomic DNA from honey than the other two procedures of commercial kits. The duplex PCR amplifying DNA of 133 bp were more sensitive than that amplifying DNA of 206 bp in detecting EH in the honey mixture of KNH and EH. Agarose gel electrophoresis and IC detected the DNA of 133 bp at the ratios of down to 1% and 5% EH in the honey mixture, respectively and also revealed that several KNH products distributed by internet shopping sites were actually EH. In conclusion, the duplex PCR with subsequent IC could also discriminate between KNH and EH and save time and labor.

A PRELIMINARY STUDY ON THE CHARACTERIZATION OF HONEY BY NEAR INFRARED SPECTROSCOPY

  • Davies, Anthony M.C.;Radovic, Branka;Fearn, Tom;Anklam, Elke
    • 한국근적외분광분석학회:학술대회논문집
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    • 한국근적외분광분석학회 2001년도 NIR-2001
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    • pp.1052-1052
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    • 2001
  • Hear infrared (NIR) spectra were measured, at five temperatures, for forty-eight samples of honey, from a variety of geographical and botanical sources, and the data has been used to explore the possibility of using NIR spectroscopy for testing label claims concerning the geographical and botanical source of honey being offered for sale to the public. These results demonstrate that the successful characterization of the botanical source of a honey may be obtained by NIR spectroscopy. Further work with large numbers of samples and groups will be required to realized this potential. Additional analysis of these data suggest that research into new ways of obtaining information on the change of absorption with temperature might be beneficial for a range of technologies.

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LC-MS/MS를 이용한 벌꿀 중 스트렙토마이신 분석 (Analysis of streptomycin in honey by LC-MS/MS)

  • 심영은;명승운
    • 분석과학
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    • 제21권5호
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    • pp.424-431
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    • 2008
  • 스트렙토마이신은 아미노글리코사이드계 항생제중의 하나로써 가축, 가금류의 질병 치료와 예방에 널리 사용되고 있다. 국내에서는 양봉용으로는 허가되어 있지 않지만 일부 국가에서는 유럽형 부저병과 같은 세균성 벌꿀 질병의 치료에 사용되는 것으로 알려져 있다. LC-MS/MS를 이용하여 벌꿀 중에 잔류하는 스트렙토마이신(streptomycin)을 분석하는 방법을 확립하였다. 확립된 분석법은 재현성과 정밀성을 높이고 미량까지 검출할 수 있도록 회수율을 높이기 위하여 정제 및 추출과정을 최적화 하였으며, 효과적인 분석을 위해서 액체 크로마토그래피(HPLC) 와 텐뎀 질량분석법(tandem mass spectrometry)의 조건들을 최적화하였다. 확립된 방법은 5.0~50.0 ug/kg 농도에서 5.5~14%인 정밀성(RSD)을 나타내었으며, bias로써 -10.0~8.0%의 정확도를 나타내었다. 한편, 스트렙토마이신을 벌꿀 공 시료에 10.0 ug/kg의 농도로 소량첨가한 후 얻은 회수율은 74%이었고, 정량한계(LOQ)는 0.75 ug/kg이었다. 확립된 벌꿀 중 스트렙토마이신 분석법을 이용하여 실제 벌꿀시료에 적용한 결과 몇몇 시료에서 소량의 스트렙토마이신이 검출되었다.

Apis cerana Beekeeping and Sacbrood Disease Management in Vietnam: Review

  • Thai, Pham Hong;Huyen, Nguyen Thi;Toan, Tran Van;Jung, Chuleui
    • 한국양봉학회지
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    • 제33권4호
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    • pp.269-275
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    • 2018
  • Beekeeping status of Apis cerana with emphasis of experiences overcoming sacbrood virus disease are presented. Social bee fauna are rich in Vietnam with 6 honeybee species (Apis laboriosa, Apis dorsata, Apis mellifera, Apis cerana, Apis andrenifomis, Apis florea); 8 stingless bee species (Trigona laeviceps, Trigona ventralis, Trigona pagdeni, Trigona gressitti, Trigona fuscobalteata, Trigona capenteri, Trigona scintillans Trigona iridipenis) and 2 bumble bee species (Bumbus haemorrhoidalis, B. breviceps). All of them are native except A. mellifera which was introduced in1887. These bees are slated for conservation by the Ministry of Agriculture & Rural Development. Honey and other bee products are mainly harvested from 3 species including A. cerana, A. mellifera and A. dorsata. The manageable species (A. cerana and A. mellifera) are increasing in number, reaching about 1,500,000 beehives. Vietnam is the second largest honey exporter in Asia, with a total of about 48,000 tons of honey exported to the international market in 2014. A. cerana plays an important role in poverty alleviation in mountainous and remote areas of Vietnam. Honeybee suffers from various diseases of Sacbrood virus disease (SBV), European foulbrood (EFB), Nosema, and parasitic mites of Tropilaelaps mercedes and Varroa destructor. Most of these diseases can be resolved with biocontrol methods. For the parasitic mites, Vietnamese beekeepers usually apply formic acid.

대전광역시 양봉농가의 꿀벌질병 감염률 조사 (Prevalence of honeybee (Apis mellifera) disease in Daejeon)

  • 김영주;김종호;오윤희;이상준;송선경;정은영;이상준;이석주;문병천
    • 한국동물위생학회지
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    • 제39권4호
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    • pp.253-258
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    • 2016
  • This study was conducted to investigate the prevalence of honey bee (Apis mellifera) disease in Daejeon. From May to September in 2014, 63 samples were collected from 63 apiculture farms in the regions and reverse transcriptase-polymerase chain reaction (RT-PCR) and polymerase chain reaction (PCR) was conducted. A total of 11 infectious pathogens, including 6 virus, 2 bacteria, 2 fungi, and 1 parasite, were investigated in honeybee colonies suffering from symptom of sudden collapse, depopulation or paralysis. The infectious pathogens and infection rates among 63 honeybee colonies detected were as follows: sacbrood virus (12.7%), chronic bee paralysis virus (1.6%), stonebrood (11.1%), American foulbrood (19.0%), European foulbrood (6.3%), respectively. The result indicate that foul-brood was most prevalent disease in apiculture farms in Daejeon area.

마그레브(Maghreb)의 식문화 -알제리아를 중심으로- (Food of Maghreb -Algerian food in particular-)

  • 전희정
    • 한국식생활문화학회지
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    • 제11권5호
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    • pp.651-661
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    • 1996
  • Algeria is located at the Mediterranean coast of north Africa, 90% of its population is concentrated in the coastal area which is mainly devoted to agriculture. Highland steppe and vast desert climate have determined its food culture. Long arab domination has influenced food of Algeria which has also undergone certain impact of Spanish, Turkish and French occupation. A variety of agricultural products, vegetables, fruits, spices and herbs have determined cooking method and food combination of Algeria. It use neither pork nor alcohol. Its main food consists of bread made from wheat flour and couscous cooked with semoule, Mechuwi, roast lamb and chorba, mixed soup are also typical foods of this region. For climatic reason lamb and chicken are prefered. Energy efficient method is applied to cooking through using oil for saute and water for boiling. Under european influence, Algerian salad used dressing for leaf vegetables, root and other kind vegetables were boiled. Serving with cake and cookies as dessert may possibly be the influence from the French occupation. The cake and cookie are made of wheat flour or other grain flour and take a specific form to be fried sweet with honey. Herbs and spices are widely used in cooking which are easily cultivated in household: mint, basil, rosemary, bayleaf, thyme, sage, fennel, marjoram, coriander, celery. Garlic, onion, piment, red pepper, cinammon are also widely used in an ordinary cooking. Reasonable food combination and economic cooking method could be subject of Algerian food study.

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꿀벌 6종 주요 병원체에 대한 초고속 다중 PCR 검출법의 개발 (Development of Ultra-Rapid Multiplex PCR Detection against 6 Major Pathogens in Honeybee)

  • 임수진;김정민;이칠우;윤병수
    • 한국양봉학회지
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    • 제32권1호
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    • pp.27-39
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    • 2017
  • 꿀벌 6종 주요 감염성 질병을 동시 진단하기 위한 PCR-chip 기반 초고속 다중 PCR 진단법을 개발 하였다. 6종 주요 꿀벌 감염성 병원체들은, 세균성 질병인 미국부저병의 원인균, Paenibacillus larvae와 유럽부저병의 원인균인 Melissococcus plutonius, 또한 진균인 Ascosphaera apis(백묵병), Aspergillus flavus(석고병)와 Nosema apis, Nosema ceranae(노제마병)를 선발하였다. 개발된 PCR-chip 기반 초고속 다중 PCR은, 꿀벌 주요 병원체 6종에 대하여 각기 $10^3$ 분자이상이 존재할 경우 모두 성공적 증폭을 보였으며, 증폭여부의 확인에 걸린 시간(Ct-time)은 6종 중 4종은 9분 내외, 2종은 7분 내외이었으며, 총 40회전의 PCR은 11분 42초, 융점분석 1분 15초로 총 PCR분석에 소요된 시간은 12분 57초(40회전 및 융점분석)이었다. 표준 DNA 기질을 사용한 PCR-chip 기반 초고속 다중 PCR은 100%에 근접한 정확도를 보였으며, 꿀벌 genomic DNA를 사용한 실험에서 false-amplification은 발견되지 아니하였다. PCR-chip 기반 초고속 다중 PCR은 실험실 내 초고속 진단 뿐 아니라 양봉 현장에서도 신속하고 효율적인 병원체 검출법이 될 것으로 기대한다.