Abstract:
본 발명은 C3G 색소의 안정성이 향상된 반건조 오디의 제조방법 및 이를 이용하여 제조된 반건조 오디에 관한 것이다. 본 발명의 C3G 색소의 안정성을 향상시킨 반건조 오디의 제조방법은 오디와 설탕을 혼합하여 혼합물을 제조하는 제1단계, 상기 혼합물에 구연산을 첨가한 후, 이를 숙성시킨 다음 오디숙성물을 분리하는 제2단계 및, 상기 분리된 오디숙성물은 상기 오디중량의 40%이하가 될 때까지 열풍건조하여 반건조 오디를 제조하는 제3단계를 포함하여 구성된다. 본 발명에 의해 C3G 안정성이 향상된 반건조 오디를 제공함으로써, 이 반건조 오디를 다양한 식품에 첨가하여 조리 또는 가공할 수 있으므로 오디의 식품 이용 기대성이 높아져 오디 소비 촉진에 기여할 수 있게 된다.
Abstract:
PURPOSE: A composition for enhancing immunity of honey bees is provided to protect honey bees from death by preventing diseases due to virus and to improve a physiological environment for honey bees, thereby extending life span of honey bees and enhancing immunity. CONSTITUTION: A composition for enhancing immunity of honey bees contains 0.001-0.01 wt% of alkaloid with antiviral activity against virus causing sacbrood. The alkaloid is derived from pollen of Brassica campestris subsp. napus var. nippo-oleifera Makino, acorn flowers, chestnut blossoms, or a mixture thereof. The composition further contains flavonoid with antiviral activity and antibacterial activity. [Reference numerals] (AA) After composition for enhancing immunity treatment; (BB) Before composition for enhancing immunity treatment; (CC) Spot where bacterial activity does not appear; (DD) Spot where bacterial activity appears
Abstract:
PURPOSE: A producing method of a honeycomb extract is provided to 100% recycle surplus honeycombs generated as a beekeeping byproduct. CONSTITUTION: A producing method of a honeycomb extract comprises the following steps: double-boiling honeycombs for completely melting, and cooling the molten honeycombs for collecting beeswax from the upper side; separating honey bee residues from the liquid; condensing the supernatant to obtain a product in a honey form; and bottle packing the obtained extract.
Abstract:
PURPOSE: A PCR primer set which is able to detect a specific gene fragment of kashmir bee virus(KBV) of honey bee is provided to accurately and sensitively detect KBV. CONSTITUTION: A PCR primer set for detecting Kashmir bee virus(KBV) comprises KIRT-F primer and KIRT-R primer. A forward primer KIRT-F has 5'-GGGCTTTATAGCTCATTTGATGG-3' of sequence number 1. The reverse primer KIRT-R has 5'-CTTGCGGACAGTTTTACTCCA-3' of sequence number 2. The detection of KBV infection is performed by PCR using the PCR primer set and confirming PCR product.
Abstract:
PURPOSE: A PCR primer set for diagnosing IAPV(Israel acute bee paralysis virus) is provided to detect an RNA fragment which is specific to IAPV and diagnose an infection of IAPV. CONSTITUTION: A primer set for diagnosing IAPV(Israel acute bee paralysis virus) comprises a primer set of sequence numbers 1 and 2. A kit for diagnosing IAPV infection contains an oligonucleotide primer set, reverse transcriptase, and a reagent. A method for diagnosing IAPV infection comprises: a step of isolating total RNA from a honeybee sample; a step of amplifying a target sequence through RT-PCR; and a step of detecting an amplified product.
Abstract:
PURPOSE: Provided is a method for mass proliferation of Bombus, ignitus Smith, which increases an oviposition rate of the Bombus, ignitus Smith, and which increases an oviposition efficiency and maximizes a productivity of bee group, and which improves a quality of the produced bee group, and substantially reduces costs. CONSTITUTION: The method comprises simultaneously introducing a worker of Bombus ignitus or Bombus terrestris which is an oviposition promoter, and a queen bee of Bombus ignitus, in order to improve an oviposition of the worker. In the method, worker of less than 3 days or more than 3 days after eclosion is anesthetized. The number of worker introduced as an oviposition promotor is 2. Breeding temperature is 27 deg.C and breeding humidity is relative humidity 65%, when field collected Bombus ignitus is bred at indoor environment.