• 제목/요약/키워드: sucrose hydrolysis

검색결과 80건 처리시간 0.03초

숙성지황의 당류와 미생물에 에탄올 첨가가 미치는 영향 (Influence of Ethanol Addition on Sugars and Microbial Growth of Rehmannia glutinosa Rhizome with Aging Treatment)

  • 장귀영;최재훈;김형돈;서경혜;이승은;지윤정;강민혜;김동휘;최수지
    • 한국식품영양학회지
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    • 제33권3호
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    • pp.251-256
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    • 2020
  • The aging treatment was applied to Rehmannia glutinosa rhizome (RGR) to improve the digestibility by the enzymatic hydrolysis of undigestible sugars. However, RGR spoils easily during the aging treatment. Thus, the purpose of this study was to investigate the influence of ethanol addition as preservatives on sugars and microbial growth of aged RGR. The RGR was treated with the addition of ethanol (0~10%) at 55℃ for eight days. Reducing, free sugars, and total bacterial counts of RGR with ethanol concentrations were analyzed during the aging periods. The aged RGR with 0-2% ethanol appeared spoiled in appearance, and total bacterial counts of these samples increased from 1.1×105 to 2.2×107 CFU and then decreased again. When treated with 4~10% ethanol, the total bacterial counts of aged RGR decreased by more than 99.9% at eight days. In all samples, reducing and digestible sugars increased, and stachyose decreased by the aging treatment. Sucrose content was highest in the 6% ethanol sample (18.2% at six days). These results indicate that the ethanol addition can be applied to the aging treatment of the RGR for improving qualities (sweetness, digestibility, and microbial growth), and can be considered for the stable production of high quality aged RGR.

점질물 제거가 다시마 추출액의 물리화학적 특성에 미치는 영향 (Effect of Removal of Viscous Materials on Physicochemical Properties of Sea Tangle Extract)

  • 이정근;이승렬;김우정
    • 한국식품과학회지
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    • 제26권2호
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    • pp.127-132
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    • 1994
  • 알긴산 제거시 전반적으로 고형분 및 단백질 수율이 감소하였고 UF처리가 $CaCl_2$ 첨가시 보다 더 뚜렸한 감소를 보였으며 점도는 알긴산 제거전 $84{\sim}94\;cps$이었던 것이 10cps로 감소하였고 탁도 또한 현저히 감소하였다. 아미노태 질소의 회수량은 $CaCl_2$ 첨가보다 UF처리한 것이 적었고 특히 NaCl을 첨가시 가장 적게 나타났으며 mannitol은 추출방법에 따른 변화가 없었다. 유기산은 oxalic acid의 함량이 높았으며 효소처리 후 NaCl 1.5%를 첨가하여 추출한 시료가 전반적으로 함량이 높게 나타났으며 핵산 조성은 분말과 2시간 열수추출의 경우 4가지 핵산이 비교적 균등한 분포를 보였으나 알긴산 제거시 일부 핵산이 함께 제거되어 핵산조성비율에 영향을 주었다. 특히 $CaCl_2$에 의한 침전제거는 IMP가 전부 그리고 UMP가 많이 손실되었으며 UF처리가 $CaCl_2$ 방법보다 핵산손실이 훨씬 적었다. 추출액의 아미노산 조성은 전체함량 중 aspartic acid와 glutamic acid가 80% 이상을 차지하고 있고 그 밖의 아미노산 함량은 대단히 적게 나타났으며 tryptophan, proline등 일부 아미노산은 검출되지 않았다.

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효소 가수 분해에 의한 돼지 감자로 부터 과당 생산 - 제1보 : 고정화 이눌라아제의 제조와 성질 - (Production of Fructose from Jerusalem Artichoke Tubers By Enzymatic Hydrolysis - I. Preparation and Properties of Immobilized Inulase -)

  • 김우연;변시명;남백희
    • 한국식품과학회지
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    • 제11권4호
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    • pp.283-290
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    • 1979
  • Kluyveonyces fragilis로부터 정제한 ${\beta}-fructosidase$ (inulase)를 Tygon 관과 aminoethyl-cellulose에 고정화 시킨후 효소의 일반적 성질을 알아 보았다, Tygon곤에 효소를 고정화 시키는데 있어서는 크로로포름 용액에서 65^{\circ}C의 조건으로 실란화(silanization) 시킨 다음 10 % 글루타르알데히드로 처리하는 것이 매우 중요한 처리 조건인 반면 2 % 글루타르알데히드 처리가 aminoethyl-cellulose에 inulase를 고정화 시키는데 매우 효과적이 었다. Tygon관에 고정화 시킨 inulase는 g matrix당 11.5 units의 inulase 역가로 보여 주었고 효소 역가의 회수율은 22.5 %인 반면 aminoethyl-cellulose에 고정화 시킨 제품은 g matrix 당 39.3 units, 53.4 % 효소 역가 회수율을 보여 주었다. 두 고정화 제품을 사용하여 invertase(기질이 sucrose) inulase (기질이 inulin) 역가에 대한 효소 안정성, pH 효과, 온도 효과 및 기질 효과를 살펴 보았다.

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Lipomyces starkeyi KSM 22 Glucanhydrolase 용액의 치은 섬유아세포에 대한 영향 (Effects of Lipomyces starkeyi KSM 22 Glucanhydrolase on human gingival fibroblasts)

  • 윤현정;정현주;김옥수;김도만
    • Journal of Periodontal and Implant Science
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    • 제32권3호
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    • pp.665-683
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    • 2002
  • A novel glucanhydrolase from a mutant of Lipomyces starkeyi KSM 22 has additional amylase activity besides mutanolytic activity and has been suggested as promising anti-plaque agent. It has been shown effective in hydrolysis of mutan, reduction of mutan formation by Streptococcus mutans and removal pre-formed sucrose-dependent adherent microbial film and has been strongly bound to hydroxyapatitie. These in vitro properties of Lipomyces starkeyi KSM 22 glucanhydrolase are desirable for its application as a dental plaque control agent. In human experimental gingivitis model and 6 month clinical trial, mouthrinsing with Lipomyces starkeyi KSM 22 dextranase was comparable to 0.12% chlorhexidine mouthwash in inhibition of plaque accumulation and gingival inflammation and local side effect was negligible. This study was aimed to evaluate the cytotoxic effect of Lipomyces starkeyi KSM 22 glucanhydrolase on human gingival fibroblasts. Primary culture of human gingival fibroblasts at the 4th to 6th passages were used. Glucanhydrolase solution was made from lyophilized glucanhydrolase powder from a mutant of Lipomyces stakeyi KSM 22 solved in PBS and added to DMEM medium to the final concentration of 0.5, 1, and 2 unit. Cells were exposed to glucanhydrolase solution or 0.1 % chlorhexidine and the cells cultured in DMEM with 10% FBS and 1% antibiotics as control. After exposure, the morphological change, cell attachment, and cell activity by MTT assay were evaluated in 0.5, 1.5, 3, 6, 24 hours after treatment. The cell proliferation and cell activity was also evaluated at 2 and 7 days after 1 minute exposure, twice a day. The cell morphology was similar between the Lipomyces smkeyi KSM 22 glucanhydrolase groups and control group during the incubation periods, while most fibroblasts remained as round cell regardless of incubation time in the chlorhexidine group. The numbers of the attached cells in the glucanhydrolase groups were comparable to that of control and significantly higher than the chlorhexidine group. The numbers of the proliferated cells in the glucanhydrolase groups at 7 days of incubation were comparable to the control group and higher than the chlorhexidine group. The cell activity in glucanhydrolase groups paralleled with the increased cell number by attachment and proliferation. According to these results, Lipomyces starkeyj KSM 22 glucanhydrolase has little harmful effect on attachment and proliferation of human gingival fibroblasts, in contrast to 0.1% chlorhexidine which was cytotoxic to human gingival fibroblasts. Therefore this glucanhydrolase preparation is considered as a safe and promising agent for new mouthwash formula in the near future.

김치 분리균인 Bacillus sp. JK-43이 생산하는 Cyclodextrin Glucanotransferase의 생산 및 특성 (Production and Characterization of Cyclodextrin Glucanotransferase fronm Bacillus sp. JK-43 Isolated from Kimchi)

  • 전홍기;배경미;김영희;백형석
    • 한국식품영양과학회지
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    • 제29권1호
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    • pp.41-48
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    • 2000
  • 김치 시료로부터 자동산화되지 않으며 열 및 중성 pH에서 안정한 AA 유도체인 AA-2G를 생산할 수 있는 당전이활성을 가진 CGTase 생산균주를 분리하였고, 분리균주의 형태학적, 배양학적, 생리학적 성질 및 16s-rDNA sequences를 조사한 결과 그람 양서의 간균으로 호기성이며 내생포자를 형성하는 전형적인 중온성 Bacillus sp. JK-43으로 동정되었다. Bacillus sp. JK-43의 CGTase는 AA-2G 뿐만 아니라 AA-6G로 추정되는 물질을 함께 생산하였으며, 효소 최적생산조건은 1.0% soluble starch, 1.0% yeast extract, 1.0% $Na_2CO_3\;0.1%\;K_2HPO_4,\;그리고\;0.02%\;MgSO_4{\cdot}7H_2O$가 함유된 배지에서 pH 7.0, $37^{\circ}C$에서 26시간 동안 진탕배양하였을 때였다. 각종 당공여채에 따른 Bacillus sp. JK-43의 AA-2G 생산성을 조사한 결과 ${\beta}-CD$에서 가장 높은 AA-2G 생산성을 보였으며, 식혜제도페액인 엿기름 및 밥당화액에서도 비교적 높은 AA-2G 생산성을 보였다. 또한 여러 가지 당수용체에 대한 JK-43의 CGTase의 당전이 반응을 검토한 결과 sucrose, mannitol 및 inositol에서 높은 당전이 수율인 70~90%를 나타내었다.

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실험적 치은염에서 dextranase 함유 구강 세정액의 양치 효과 (The Effect of Dextranase-Containing Mouthwash in Human Experimental Gingivitis)

  • 손은주;김영준;김도만;정현주
    • Journal of Periodontal and Implant Science
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    • 제31권2호
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    • pp.401-420
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    • 2001
  • A novel glucanhydrolase from a mutant of Lipomyces starkeyi(KSM 22)has been shown effective in hydrolysis of mutan, reduction of mutan formation by Streptococcus mutans and removal pre-formed sucrose-dependent adherent microbial film and Lipomyces starkeyi KSM 22 dextranase has been strongly bound to hydroxyapatitie. These in vitro properties of Lipomyces starkeyi KSM 22 dextranase are desirable for its application as a dental plaque control agent. This study was performed to determine oral hygiene benefits and safety of dextranase(Lipomyces starkeyi KSM 22 dextranase)-containing mouthwash in human experimental gingivitis. This 3-week clinical trial was placebo-controlled double-blind design evaluating 1U/ml dextranase mouthwash and 0.12% chlorhexidine mouthwash. A total 39 systemically healthy subjects, who had moderate levels of plaque and gingivitis were included. At baseline, 1, 2 and 3 weeks, subjects were scored for plaque(Silness and $L{\ddot{o}e$ plaque index and plaque severity index), gingivitis($L{\ddot{o}e$ and Silness gingival index), and at baseline and 3 weeks of experiment, subjects were scored for plaque(Turesky-Quingley-Hein's plaque index and plaque severity index), tooth stain(Area and severity index system by Lang et al). Additionally, oral mucosal examinations were performed and subjects questioned for adverse symptoms. Two weeks after pre-experiment examinations and a professional prophylaxis, the subjects provided with allocated mousewash and instructed to use 20-ml volumes for 30s twice dailywithout toothbrushing. All the groups showed significant increase in plaque accumulation since 1 week of experiment. During 3 weeks' period, the dextranase group showed the least increase in plaque accumulation of Silness and $L{\ddot{o}e$ plaque index, compared to the chlorhexidine and placebo groups, but chlorhexidine group showed the least increase inplaque accumulation of Turesky-Quingley-Hein's plaque index. As for gingival inflammation, all the groups showed significant increase during 3 weeks of experiment. The dextranase group also showed the least increase in gingival index score, compared to the chlorhexidine as well as the placebo groups. Whereas the tooth stain was increased significantly in the chlorhexidine group, compared to the baseline score and the placebo group since 3 weeks of mouthrinsing. It was significantly increased after 3 weeks in the dextranase group, still less severe than the chlorhexidine group. As for the oral side effect, the dextranase group showed less tongue accumulation, bad taste, compared to the chlorhexidine group. From these results, mouthrinsing with Lipomyces starkeyi KSM 22 dextranase was comparable to 0.12% chlorhexidine mouthwashin inhibition of plaque accumulation and gingival inflammation and local side effects were if anything less frequent and less intense than chlorhexidine, in human experimental gingivitis. All data had provided positive evidence for Lipomyces starkeyi KSM 22 dextranase as an antiplaque agent and suggested that further development of dextranase formulations for plaque control are warranted.

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Dextranase 함유 구강 세정액의 치태 억제 및 치은염 예방 효과에 관한 임상적 연구 (A Clinical Trial of Dextranase-Containing Mouthwash on the Inhibition of Plaque Formation and Gingivitis)

  • 송우성;손은주;김도만;정현주
    • Journal of Periodontal and Implant Science
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    • 제31권2호
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    • pp.371-388
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    • 2001
  • A novel glucanhydrolase(DXAMase) from a mutant of Lipomyces starkeyi(KSM 22) has been shown effective in hydrolysis of mutan, reduction of mutan formation by Streptococcus mutans and removal pre-formed sucrose-dependentadherent microbial film and DXAMase has been strongly bound to hydroxyapatitie. These in vitro properties of Lipomyces starkeyi DXAMase are desirable for its application as a dental plaque control agent. This study was performed to determine the adjunctive oral hygiene benefits and safety of dextranase(Lipomyces starkeyi KSM 22 DXAMase)-containing mouthwash when used alongside normal tooth-brushing. This 6-month clinical trial was placebo-controlled double-blind design evaluating 1U/ml dextranase mouthwash and 0.12% chlorhexidine mouthwash. A total 39 systemically healthy subjects, who had moderate levels of plaque and gingivitis were included. At baseline, 1, 3 and 6 months, subjects were scored for plaque accumulation(Turesky modification of Quingley-Hein's plaque index), gingivitis status($L\ddot{o}e$ and Silness gingival index), and tooth stain(Area and severity index system by Lang et al). Additionally, oral mucosal examinations were performed and subjects questioned for adverse symptoms. Two weeks after pre-experiment examinations and a professional prophylaxis, the subjects provided with allocated mousewash and instructed to use 20-ml volumes for 30s twice daily after toothbrushing. All the groups showed significant increase in plaque accumulation since 1 month of experiment. During 6 months' period, the Dextranase mouthwash group showed the least increase in plaque accumulation, compared to the Chlorhexidine mouthwash and placebo groups. As for gingival inflammation, all the groups showed significant increase during 6 months of experiment. The Experimental group(Dextranase mouthwash) also showed the least increase in gingival index score, compared to the Positive control(Chlorhexidine mouthwash)as well as the Negative control(placebo)groups. Whereas the tooth stain was increased significantly in the Positive control group, compared to the baseline score and the Negative controlgroup since 3 months of mouthrinsing. It was significantly increased after 6 months in the Experimental group, still less severe than the Positive control group. As for the oral side effect, the Experimental group showed less tongue accumulation, bad taste, compared to the Positive control group. From these results, mouthrinsing with Lipomyces starkeyi KSM 22 dextranase provided adjunctive benefits to toothbrushing, comparable to 0.12% chlorhexidine mouthwash in inhibition of plaque accumulation and gingival inflammation and local side effects were if anything less frequent and less intense than chlorhexidine, with long-term use of the mouthwash. All data had provided positive evidence for Lipomyces starkeyi KSM 22 dextranase as an antiplaque agent and suggested that further development of dextranase formulations for plaque control are warranted.

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산가수분해한 유채대로부터 유리당의 분리 및 이의 잔사로부터 펠릿의 제조 (Separation of Reducing Sugars from Rape Stalk by Acid Hydrolysis and Fabrication of Fuel Pellets from its Residues)

  • 양인;안병준;김명용;오세창;안세희;최인규;김용현;한규성
    • 한국자원식물학회지
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    • 제27권1호
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    • pp.60-71
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    • 2014
  • 본 연구는 유채의 바이오리파이너리 원료화 가능성을 확인하기 위하여 유채대를 DW, AA, OA, SA 및 SH 용액에 침지하였다. 먼저 침지 유채대의 원소를 분석한 결과, 침지를 통하여 질소, 황, 염소의 함량이 효과적으로 감소되는 것을 확인하였다. 이 외에 침지액의 농도와 침지시간을 실험인자로 침지액 내에 존재하는 glucose, xylose, arabinose와 같은 유리당의 양을 조사하였는데, DW- 및 SH-침지액에서는 각각 xylose와 sucrose만 그리고 SA- 및 OA-침지액에서는 소량의 glucose만 검출되었다. 그러나 AA-침지액에서는 많은 양의 glucose와 소량의 arabinose까지 분석되었다. 한편, 유채대 침지에 사용된 산용액의 종류와 농도(1%, 2%)에 따른 glucose 양을 분석한 결과, AA를 침지액의 조제를 위한 산으로 사용하고 AA의 농도를 1%로 조절하는 것이 유채대로부터 효과적으로 glucose를 가수분해할 수 있는 조건인 것으로 조사되었다. 침지시간의 영향을 보면, 72 hr-침지에서 가장 많은 양의 glucose가 검출되었으며, 120 hr까지의 침지시간 연장은 유리되는 glucose 양에 부정적인 영향을 미쳤다. 다음으로, DW, AA, OA 용액에 침지시킨 유채대를 이용하여 펠릿을 제조하였는데, 이 때 산의 농도 그리고 침지시간(24, 72, 120 hr)을 실험 인자로 사용하였으며, 이렇게 제조된 펠릿의 함수율, 겉보기밀도, 회분량, 발열량, 내구성을 측정하였다. 침지 유채대 펠릿의 겉보기 밀도와 발열량은 무침지 유채대 펠릿과 비교하여 크게 높았으며, 실험 인자와 상관없이 EN 규격의 A등급 기준($${\leq_-}600kg/m^3$$, $${\qeq_-}14.1MJ/kg$$)을 각각 상회하였다. 유채대의 침지는 무침지 유채대의 회분량(8.9%)과 비교하여 회분량을 크게 감소시켰으며, 특히 AA-와 DW-침지가 유채대의 회분량 감소에 효과적인 것으로 나타났다. 또한 침지 유채대의 회분량은 EN 규격의 A등급 기준($${\leq_-}5.0%$$)을 만족하였다. 침지 유채대로 제조한 펠릿의 내구성은 전반적으로 무침지 유채대 펠릿(97.40%)보다 낮았으며, 특히 OA-2%에 120 hr 침지시킨 유채대 펠릿을 제외하고 나머지 조건은 EN 규격의 B등급($${\qeq_-}96.00%$$) 기준에 만족하지 않는 것으로 조사되었다. 침지 유채대의 원소 및 유리당 분석 그리고 펠릿의 품질 시험 결과를 종합하면, 1% 농도의 AA 용액에 유채대를 72 hr동안 침지시키는 것이 유채대의 바이오에탄올 및 펠릿 원료화를 위한 최적조건이라는 결론을 얻었다. 따라서 이 조건에서 1 kg의 유채대를 침지시켰을 경우, 산술적으로 바이오에탄올 생산용 원료인 50 g의 glucose를 얻을 수 있으며, 나머지 950 g의 잔사는 아그로펠릿의 원료로 사용이 가능할 것으로 생각한다. 그러나 AA-침지 유채대로 제조한 펠릿의 낮은 내구성 문제를 해결하기 위하여 세분화된 범위의 침지 조건 탐색, 목분과의 혼합 펠릿 제조, 바인더의 첨가 등과 같은 추가 연구가 수행되어야 할 것으로 생각한다.

급성(急性) 기아(饑餓)마우스의 간단백질(肝蛋白質), 핵산(核酸) 및 Guanine Deaminase 활성(活性)에 관(關)한 연구(硏究) (A Study on The Content of Liver Protein, Nucleic Acids, and Guanine Deaminase Activity of Mouse During Acute Starvation)

  • 박승희;김승원
    • Journal of Nutrition and Health
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    • 제1권2호
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    • pp.107-115
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    • 1968
  • Number of aspects, not only nutritional but social as well as political involved in human starvation pose nowadays global problems. In order to help establish the minimum nutritional requirements in the daily life of a man and to free people as well from either undernourishment, malnutrition or even starvation many workers have devoted themselves so far on the research programs to know what and how number of metabolic events take place in animals in vivo. It is the purpose of the present paper to examine in effect to what extent both of the protein and nucleic acids (DNA & RNA) together with an enzyme, guanine deaminase, which converts guanine into xanthine and in turn ends up to uric acid as an end product, undergo changes, quantitatively during acute starvation, using the mouse as an experimental animal. The mouse was strictly inhibited from taking foods except drinking water ad libitum and was sacriflced 24, 48, and 72 hours following starvation thus acutely induced. The animals consisted of two experimental groups, one control and another starvation groups, each being consisted of 6-24 mice of whose body weights ranged in the vicinity of 10 g. The animals were sacriflced by a blow on the head, followed by immediate excision of their livers into ice-cold distilled water, washing adherent blood and other contaminant tissues. The liver was minced foramin, by an all-glass homogenizer immersing it in an ice-bath, followed by subsequent fractionatin of the homogenate (10% W/V in 0.25M sucrose solution made up with 0.05M phosphate buffer of pH 7.4). For the liver protein and guanine deaminase assay, the 10% homogenate was centrifuged at 600 x g for 10 minutes to eliminate the nuclear fraction; and for the estimation of DNA and RNA, the homogenate was prepared by the addition of 10% trichloroacetic acid in order to free the homogenate from the acid-soluble fraction, the remaining residue being delipidate by the addition of alcohol and dried in vacuo for later KOH (IN) hydrolysis. The changes in body and liver wegihts during acute starvation were checked gravimetrically. Protein contents in the liver were monitored by the method of Lowry et al; and guanine deaminase activities were followed by the assay of liberated ammonia from the substrate utilizing the Caraway's colorimetry. The extraction of both DNA and RNA was performed by the Schmidt-Thannhauser's method, which was followed by Marmur's method of purification for DNA and by Chargaff's method of purification for RNA. The determinations of both DNA and RNA were carried out by the diphenylamine reaction for the former and by the orcinol reaction for the latter. The following resume was the results of the present work. 1. It was observed that the body as well as liver weights fall abruptly during starvation, and that the loss of body weight showed no statistical correlation with the decreases in the content of liver protein. 2. The content of liver protein and activity of liver guanine deaminase activity as well decline dramatically, and the specific activities of the enzyme (activity/protein), however, decreased gradually as starvation proceeded. 3. Both of the nucleic acids, DNA and RNA, showed decrements in the liver of mouse during acute starvation; the latter, however, being more striking in the decline as compared to the former. 4. The decreases in the liver protein content as resulted from the acute starvation had no statistically significant correlation with the decrements of DNA in the same tissue, but had regressed with a significant statistical correlation with the fall of RNA in the tissue. 5. The decrease in the activity of guanine deaminase in the liver of mouse during acute starvation was functionally more proportional to the decrease in RNA than DNA, and moreover correlated with the changes in the content of the liver protein. 6. The possible mechanisms involved during in this acute starvation as bring the decreases in the contents of DNA, protein, and guanine deaminase were discussed briefly.

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인삼식물의 종자발육 과정에 있어서의 생리화학적 연구 (Studies on the Physiological Chemistry of Seed Development in Ginseng Seed)

  • 양희천
    • 한국작물학회지
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    • 제17권
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    • pp.115-133
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    • 1974
  • 인삼 종자의 결실과 최아과정중에서 일어나는 물질대사의 기본적 소인을 알고저 화기형성초기로부터 개화기까지, 결실초기부터 홍숙기까지, 그리고 최아과정중 화학성분의 변화를 추구하였다. 1. 화뢰에서는 감수분열기 이전까지 신선중, 건물중, 회수화물, 질소화합물의 변동은 그리 크지 않으며 TCA가용성인, 특히 유기태인의 증가와 현저하였다. 2. 감수분열기로부터 소포자기에 이르는 기간 동안 신선중, 건물중이 급격히 증가되고 전질소량이 증가하는데 불용성 질소구분은 이 시기부터 그 량이 늘어나 단백질이 합성되는 것을 의미하고 있으며 불용성 질소가 전질소의 62∼70%를 차지하고 있다. 또한 가용성 당분이 급격하게 증가되어 환원당, 비환원당이 모두 증가하나 전분의 증가는 볼 수 없고, 전인에 대한 TCA가용성인이 85.4%, TCA불용성인이 14.6%로 화뢰성장중 각각 최고, 최소치를 나타내고 있다. 3. 화분성숙기 이후와 개화기에서 특히 건물중의 증가가 현저하고 불용성질소도 계속 증가되어 총질소의 67%에 이른다. 또한 두드러진 유기태인의 저하와 갑작스런 조전분의 증가를 볼 수 있고 무기태인량이 유기태 인량을 능가하게 된다. 4. 결실기부터 홍열기까지에 있어서는 신선중량의 90%가 결실 후 3주간에 증가하는데, 1) 전질소량은 7배로 증가되었고 성숙되어 갈수록 전질소에 대한 불용성질소의 량이 커져서 65%에서 80%이상으로 상승되고 한편 가용성질소의 비율은 35%에서 20%이하로 저하되었다. 2) 전인산량도 8배로 증가되는데 홍숙이 시작되는 시기에 최고에 이르고 이때에 전인산에 대한 TCA가용성인의 비율도 가장 커서 90%에 이른다. 유기태인도 홍숙이 시작될 때까지 29배나 증가되며 지질태인, 핵산태인, 단백태인이 모두 증가되고 있다. 3) 회수화물의 증가는 신선중의 증가와 유사한데결실한지 3주 후에 최고량에 달하고 그 후는 사실상 증가하지 않으며 가용성당도 3주 후에 최고에 달했다가 일시 감소하며 홍숙기에 약간 증가하나 먼저 수준에는 이르지 못하며 조전분은 점차 증가되어 홍숙되기 일주 전에 최고량에 달하나 전 건물량의 2.36% 밖에 되지 못한다. 회수화물중 가용성당이 차지하는 비율이 훨씬 크며 완숙기에서는 가용성당분중 약80% 이상의 비환원당으로 되어 있어 인삼 종자의 주요 회수화물을 이루고 있다. 4) 한편 완숙된 종자의 배란중에는 60% 이상의 지방을 함유하고 있어 인삼 종자의 저장물질은 단백질이나 회수화물이기 보다는 주로 지방이다. 5. 최아조작중에는 배가 11월중순의 파종기까지 4.2∼4.7mm로 발육하며 충분히 흡수하여 50∼60%에 이르고, 저장지방, 단백질, 전분이 가수분해하여 가용화되고 당분, 무기태인, 인지질, 핵산태인, 단백태인과 가용성질소의 증가를 보이고 있어 세포내용물의 전이가 일어나 발아에 필요한 물질을 축적하고 있다.

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