• 제목/요약/키워드: Aspergillus usamii

검색결과 20건 처리시간 0.026초

누룩에서 분리한 우수균주에 의한 좁쌀주의 양조특성 (Zymological Properties of Foxtail Millet Wine-making by Isolated Strains from Nuruk)

  • 유철훈;홍성윤;고정삼
    • Applied Biological Chemistry
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    • 제45권3호
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    • pp.138-144
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    • 2002
  • 제주민속 좁쌀주의 품질향상을 위하여 누룩으로부터 분리한 우수균주를 이용하여 양조특성을 검토하였다. 양조효모로 Saccharomyces sp Y5-1를, 그리고 당화균으로 Aspergillus oryzae M6-1, Aspergillus awamori 6970, Aspergillus usamii mut. shirousamii 6959를 각각 사용하였다. 좁쌀주의 양조에서 발효기간 중에 총산, 가용성 고형물, 색도, 에탄올 함량은 증가하였다. 에탄올 함량은 Aspergillus awamori 6970, Aspergillus usamii mut. shirousamii 6959 누룩구가 각각 10.6%, 10.1%로 높았다. Citric acid는 발효 $1{\sim}2$일에만 검출되었고, tartaric acid는 발효 1일에 시판 누룩구에서만'51.8 ppm 검출되었다. 유기산 중에 대부분을 차지하는 lactic acid는 Aspergillus awamori 6970 누룩구, acetic acid는 시판 누룩구에서 가장 많았다. 발효 중에 xylose, arabinose, glucose, maltose가 검출되었고, glucose와 xylose가 많았다. 휘발성 향기성분으로는 acetone, ethyl acetate, methanol, ethanol, n-propanol, iso-butanol, iso-amyl alcohol이 검출되었다. 좁쌀 주의 관능검사 결과, 색과 맛에서 Aspergillus usamii mut. shirousamii 누룩구가 좋았으며, 향기에서는 서로 비슷한 기호도를 나타내었다.

곰팡이 균종을 달리한 밀가루 누룩의 탁주양조 적성 (Aptitudes for Takju Brewing of Wheat Flour-Nuluks Made with Different Mold Species)

  • 소명환
    • 한국식품영양학회지
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    • 제8권1호
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    • pp.6-12
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    • 1995
  • The purpose of this study was to examine the aptitude of wheat flour-Nuluks, for Takju brewing, which were made with Aspergillus oryzae, Rhizopus japonicus or Aspergillus usamii mut. Shirousamii, and to know the way of effective use the Aspergillus oryzae-Nuluk showed high saccharogenic activity, and Rhizopus japonicus-Nuluk high proteolytic activity. When these two Nuluks were combined, the activities of saccharogenic amylase and protease were more balanced. The Takju mash of Aspergillus oryzae-Nuluk was high in acidity and in amino acidity, and that of Rhizopus japonicus-Nuluk high in the content of free sugar, but, that of Aspergillus usamii mut. Shirousamii-Nuluk was low in amino acidity, free sugar and ethanol content. The Takju of Rhizopus japonicus-Nuluk was high in the content of suspended solid and slow in its sedimenting rate, but that of Aspergillus usamii mut. Shirousamii-Nuluk was not. The Takju which was made with combined use of Aspergillus oryzae-Nuluk and Rhizopus japonicus-Nuluk was more balanced in the composition of flavoring ingredients, and was slow in sedimenting rate of suspended solid. Moreover, it gained good result in sunsory evaluation test.

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Aspergillus usamii mut. shirousamii S1에 의한 밀가루누룩 제조시 Amylase와 Pretense의 생산조건 (Conditions for the Production of Amylase and Pretense in Marking Wheat Flour Nuluk by Aspergillus usamii mut. shirousamii S1)

  • 오명환;박서영
    • 한국식품영양학회지
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    • 제7권1호
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    • pp.51-57
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    • 1994
  • A nuluk, a Korean traditional koji for brewing, was made with wheat flour and Aspergillus usamii mot. shirousamii S1 which had strong abilities in producing amylase and protease. The cultural conditions for the production of saccharogenic and proteolytic enzymes were tested. The productivities of saccharogenic and dextrogenic enzymes were improved when nuluk was made with unsteamed wheat flour as compared with steamed one, but those of proteolytic enzyme and organic acid were reduced. The addition of water containing 0.5% of hydrochloric acid was unfavorable for the production of saccharogenic, dextrogenic and proteolytic enzymes. The optimum ratios of water added to wheat flour for the production of saccharogenic enzyme and proteolytic enzyme were 32% and 28%, respectively on the basis of wheat flour. The optimum temperatures for the production of saccharogenic enzyme and proteolytic enzyme were 36$^{\circ}C$ and 28$^{\circ}C$, respectively. The activity of saccharogenic enzyme reached its maximum after 120 hours of cultivation at 36$^{\circ}C$, but that of proteolytic enzyme 96 hours. The productivity of saccharogenic enzyme was enhanced when the nuluk was molded after 24 hours of precultivation but that of proteolytic enzyme was reduced as compared with no molding.

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Aspergillus usamii shirousamii $U_2$균(菌)의 국식배양(麴式培養)에 의(依)한 유기산(有機酸) 및 당화효소(糖化酵素) 생성(生成)에 관(關)한 연구(硏究) -제2보 항균제(抗菌劑)의 영향에 대(對)하여- (Studies on the Formation of Organic Acid and Saccharifing Amylase in Koji Culture of Aspergillus usamii shirousamii $U_2$ -Part II. Effect of antimicrobial agents-)

  • 윤복현;이석건;윤한교
    • 한국식품과학회지
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    • 제7권4호
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    • pp.238-242
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    • 1975
  • Aspergillus usamii shirousamii $U_2$ 균(菌)의 극식배양에 의한 유기산 및 당화효소생성에 미치는 영향에 대하여 실험한 결과는 다음과 같다. 1) 공시항균제(供試抗菌劑)중 일정한 농도(濃度)의 nitrofurazone과 $AF_2$의 첨가(添加)에 의하여 유기산과 당화효소(糖化酵素)의 생성이 촉진되었다. 2) 유기산의 생성은 밀가루에 $AF_2$ 10ppm 용액을 50% 첨수(添水)한 배지에서 가장 좋았다. 3) 당화효소(糖化酵素)의 생성은 밀기울에 nitrofurazone $100{\sim}500ppm$ 용액을 100% 첨수(添水)한 배지에서 가장 양호하였다.

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Bioconversion of Cyanidin-3-Rutinoside to Cyanidin-3-Glucoside in Black Raspberry by Crude α-ʟ-Rhamnosidase from Aspergillus Species

  • Lim, Taehwan;Jung, Hana;Hwang, Keum Taek
    • Journal of Microbiology and Biotechnology
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    • 제25권11호
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    • pp.1842-1848
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    • 2015
  • Cyanidin-3-glucoside (C3G) has been known to be more bioavailable than cyanidin-3-rutinoside (C3R), the most abundant anthocyanin in black raspberry (Rubus occidentalis). The aim of this study was to enhance the bioavailability of anthocyanins in black raspberry by cleaving ʟ-rhamnose in C3R using crude enzyme extracts (CEEs) from Aspergillus usamii KCTC 6956, A. awamori KCTC 60380, A. niger KCCM 11724, A. oryzae KCCM 12698, and A. kawachii KCCM 32819. The enzyme activities of the CEEs were determined by a spectrophotometric method using ρ-nitrophenyl-rhamnopyranoside and ρ-nitrophenyl-glucopyranoside. The CEE from A. usamii had the highest α-ʟ-rhamnosidase activity with 2.73 U/ml at 60℃, followed by those from A. awamori and A. niger. When bioconversion of C3R to C3G in black raspberry was analyzed by HPLC-DAD, the CEEs from A. usamii and A. awamori hydrolyzed 95.7% and 95.6% of C3R to C3G, respectively, after 2 h incubation. The CEEs from A. kawachii and A. oryzae did not convert C3R to C3G in black raspberry.

Aspergillus usamii KCTC 6954에 의한 ginsenoside Rb1로 부터 의약용 소재인 compound K로의 생물학적 전환 (Bioconversion of Ginsenoside Rb1 to the Pharmaceutical Ginsenoside Compound K using Aspergillus usamii KCTC 6954)

  • 조미나;정지은;윤현주;장경훈;지희숙;김기태;백현동
    • 한국미생물·생명공학회지
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    • 제42권4호
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    • pp.347-353
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    • 2014
  • 본 연구는 인삼의 주요성분인 ginsenoside Rb1으로부터 보다 높은 생리기능성을 갖는 것으로 알려져 있는 compound K를 생산하기 위하여 Aspergillus usamii KCTC 6954에서 유래된 ${\beta}$-glucosidase를 사용하여 생물전환을 실시하였다. 15일 동안의 배양 중, 효소활 성 측정은 ${\rho}$-nitrophenyl-${\beta}$-glucopyranoside를 기질로 하여 분해 생성되는 ${\rho}$-nitrophenol (${\rho}NP$)을 비색계로 측정함으로써 실시되었다. 그 결과로서, 균주의 성장 속도는 접종 후 6일 후 최대로 나타났으며 이때의 ${\beta}$-glucosidas 활성도는 $175.93{\mu}M\;ml^{-1}min^{-1}$로 나타났다. 또 한 효소 반응의 최적 조건은 pH 6.0 이내에서는 $60^{\circ}C$인 것으로 나타났다. 배양 중 ginsenosides 분석 결과, 배양 9일 후에는 Rb1는 Rd 로 전환되고 15 days 후에는 compound K로 순차적으로 전환되는 것으로 나타났다. 효소반응에 있어서는 Rb1는 1시간 이내에 ginsenoside Rd로 전환되었고 8시간 이후에 최종산물인 compound K가 측정되었다. 본 연구결과로부터 Rb1으로부터 주요 생물학적 전환 경로는 $Rb1{\rightarrow}Rd{\rightarrow}F2{\rightarrow}$compound K로 나타났으며 이는 차후 Rd나 compound K와 같이 강한 생리기능성을 갖지만 자연에 미 량 존재하는 물질의 대량생산에 응용될 수 있을 것으로 기대된다.

전분(澱粉)의 제조(製造)와 가공이용(加工利用)에 관(關)한 연구(硏究) - 제1보(第一報), 당화효소(糖化酵素) 생산균주(生産菌株)의 선정(選定) - (Studies on the Preparation and Utilization of Starch - 1. Selection of Two Different Strains with High Saccharifying Activity -)

  • 김호식;이서래;전남수
    • Applied Biological Chemistry
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    • 제3권
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    • pp.9-15
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    • 1962
  • 1) Rhizopus균(菌) 8주(株)와 Aspergillus속균(屬菌) 7주(株)의 당화효소생산력(糖化酵素生産力)(전분가수분해율(澱粉加水粉解率))을 비교한 결과 Rhizopus delemar ND 1과 Aspergillus usamii mut. shirousamii의 두 균주(菌株)를 각각 선정(選定)하였다. 2) Rhizopus delemar ND 1은 전분당화율(澱粉糖化率)이 높고 효소전이당(酵素轉移糖)의 생성(生成)이 적으므로 효소당화(酵素糖化) 포도당(葡萄糖)의 제조(製造)에 적합(適合)하고 Asp. usamii mut. shirousamii는 당화율(糖化率)이 약간(若干) 떨어지나 효소전이당(酵素轉移糖)의 생성(生成)이 인정(認定)되므로 특수(特殊)한 풍미(風味)를 필요(必要)로 하는 전분이(澱粉飴) 제조(製造)에 적합(適合)함을 알았다. 3) Rhizopus delemar ND 1의 당화효소(糖化酵素)를 시용(使用)한 예비시험(豫備試驗)에서 정제분말(精製粉末) 포도당(葡萄糖)을 얻을 수 있었다.

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사상균에 의한 구연산발효에 관한 연구 (제I보) 균주의 분리 및 동정 (Studies on the Citric Acid Fermentation with Fungi (Part I) Isolation and Identification of Strains)

  • 성낙계;김명찬;심기환;정덕화
    • 한국미생물·생명공학회지
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    • 제8권1호
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    • pp.47-53
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    • 1980
  • 자연계로부터 구연산생성능이 강한 균주를 분리, 선정하여 동정한 결과는 다음과 같다. 1. Aspergillus 속에 속하는 균주 579주를 분리하여 각종 실험을 한 결과 표면배양으로는 분리균 M-80, M-315를, 야내배양으로는 M-315를 공식 균으로 선정하였다. 2. 선정균 M-80, M-315를 Raper등의 분류법에 따라 동정한 결과는 각각 Aspergillus usamii mut. shirousamii, Aspergillus ficuum으로 추정되었다. 3. 발육최적배지는 맥아즙한천배지였으며 M-315는 55$^{\circ}C$, M-80은 6$0^{\circ}C$에서 30분간 처리로서 각각 사멸되었고 생육PH는 대체로 PH3~6에서 양호하였다.

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막걸리의 제조를 위한 효소제의 개발연구 1 (Studies on improvement of manufacturing method of enzymic source for Maggerley(Korea wine) brewing(I))

  • 이성범;최경환;임동순;김덕치
    • 미생물학회지
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    • 제7권4호
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    • pp.159-166
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    • 1969
  • It is necessry to develop and strengthen the activity of enzymic source which in low applied for maggerley brewing as an amylolytic and proteolytic starter, recently in this country the active and strong enzymic starter is required for the better brewing and to substitute another starch material for the present wheat flour. In this study, manufacturing method the strong enzymic source have been developed and established with use of raw wheat bran plus fungal strains of Rhizopus sp. and Aspergillus usamii the culture of starter. The results on experimental the activities of enzymic sources (stater) are as following ; 1. Method of making the enzymic source (starter) is to cultivate the strains of Asperguillus orzyae, Asp. kawachii, Asp usamii and Rhizopus sp. in the acid treated raw or heatboiled wheat bran. 2. The saccharogenic pwoer (S.P.) of enzymic source which consisted of raw bran plus fungi and cultured in it is generally stronger than those of heat-boiled bran plus fungi, the strongest power was shown in the culture of Rhizopus plus raw bran, and the next other is in mixture of Asp.usamii and Rhizopus on raw wheat bran. 3. The most strong alpha amylase activity was expressed in the plot of Asp.oryzae on heat-boiled wheat bran, the next was in the culture of Rhizopus nad Aspergillus usamii on raw wheatbran. 4. The most vigourous acidic proteinase activity was expressed in the micture of raw bran plus Asp. usamii and Rhizopus those were independentlu cu;tured before mixing for neutral proteinase activity, it was shown in the mixed culture of Asp. usamii and Rhizopus on raw wheat bran, the msot active alkaline proteinase activity of enzymic source was found in the plot of raw bran material. 5. For poly-preptidase activity in pH 6.5 it is found that the culture of Rhizopus and Asp.usamii on raw bran was most active among them of enzymic sources. 6. Generally, it is concluded that culture of fungi on acid treated raw wheat bran is stronger in its activity than those of heat boiled wheat bran, especially the culture of Rhizopus nad Asp.usamii on raw bran exhibited the most vigorous and non-polarized activity for all aspects, so it is considered to be most desirable enzymic stater in Korean Maggerley brewing and this would be able to substitute brewing material for the present wheat flour because of its strong and wide hand activity of amylolytic and proteolytic action.

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Changes in Aurantio-Obtusin and Glucoaurantio-Obtusin Content in Cassiae Semen via Treatment with a Crude Enzyme Extract from Aspergillus usamii

  • Hur, Jong-Moon;Kwon, Soon-Ho;So, Jae-Hyun;Jun, Mi-Ra;Kang, Young-Hwa;Lee, Yu-Mi;Lee, Kyung-Bok;Rhee, In-Koo;Lee, Moon-Soon;Song, Kyung-Sik
    • Journal of Microbiology and Biotechnology
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    • 제17권11호
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    • pp.1894-1897
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    • 2007
  • Cassiae Semen (seeds of Cassia tora) showed a remarkably different HPLC chromatogram after being treated with a crude enzyme extract from Aspergillus usamii. Increased and decreased compounds were identified as aurantio-obtusin and glucoaurantio-obtusin, respectively. The aurantio-obtusin content reached its maximum level ($133.58{\pm}0.39\;{\mu}g/mg$ extract) after being incubated for 50 min at $37^{\circ}C$, whereas the inactivated crude enzyme-treated control remained unchanged ($54.13{\pm}1.33\;{\mu}g/mg$). On the other hand, the glucoaurantio-obtusin content decreased by less than one-third ($51.09{\pm}1.63\;{\mu}g/mg$) ofthe untreated control ($143.19{\pm}2.12\;{\mu}g/mg$), suggesting that an increase in aurantio-obtusin content originated from the enzymatic cleavage of its glucoside glucoaurantio-obtusin.