• 한국균학회지
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• 제41권3호
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• pp.181-184
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• 2013

충남 금산군과 전남 완도군, 제주도 송악산 등지에서 서식하고 있는 야생화들로부터 Rhodosporidium fluviale 201-C-1과 Kluyveromyces thermotolerans 150-JE-2(1), Rodosporidium paludigenum과 Candida sp. 80-J-3등의 국내 미기록 효모들을 분리, 선발하여 이들의 미생물학적 특성들을 조사하였다. Rhodosporidium fluviale 201-C-1은 내염성의 무포자 효모로 의균사를 형성하였고 urease 활성을 갖고 있었다. Kluyveromyces thermotolerans 150-JE-2(1)는 내당성과 내염성을 가진 무포자효모로서 $30^{\circ}C$, pH 4.0~6.0에서 잘 생육하였다. Candida sp. 80-J-3과 Rhodosporidium paludigenum 86-J-1 균주들은 모두 무성생식을 하는 무포자 효모들이었고 YPD 배지, Vitamin-free 배지와 5% NaCl을 함유한 YPD 배지 등에서 잘 생육하였다. 또한 Candida sp. 80-J-3 균주의 urease 활성은 음성이었으나 Rhodosporidium paludigenum 86-J-1 균주는 urease 활성이 양성이면서 pH 7.0~8.0에서 잘 생육하였다.

• 한국식품영양과학회지
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• 제21권6호
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• pp.725-730
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• 1992

이담자 효모균 Rhodosporidium toruloides의 mating type A 세포에서 세포내 invertase를 정제하였다. 세포내 invertase는 배양 세포의 파쇄액을 산침전 시킨 후 그 상등액으로부터 DEAE-Sephadex A-50, SP-Sephadex C-50 column chromatography와 Sephadex G-200 gel fitration 등의 과정을 거쳐 polyacrylamide gel disc 전기영동상 단일 효소 단백질까지 정제되었다. 정제효소의 분자량은 gel filtration에 의하여 90,000이었고, SDS-PAGE상에서는 22,000 dalttons에서 단일 band를 보여 단일종의 subunit가 4개로 구성된 단백질로 추정된다.

• 생명과학회지
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• 제7권4호
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• pp.322-328
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• 1997

Two phosphorylated proteins having molecular weights of 57kD and 72kD were detected from the slubilized membrane protein fraction of mating type a cells of Rhodosporidium toruloides which belongs to heterobasidiomycetous yeast. The phosphorylation of the protein was inhibited by a sexual pheromone, Rhodotorucine A (Rh. A), which is secreted from mating type a cells. On the other hand, counterpart mating type A cells and M-39 strain which is a styerile mutant derived from a cells, had also the same two phosphorylated proteins, However, the phosphorylation of the protein from A cells, and M-39 strain were not inhibited by the Rh. A. It suggests that inhibition of the phosphorylation reaction by the Rh. A in mating type a cells is a mating-type-specific reaction that relate to transduction mechanism of sexual pheromone signaling.

• 한국균학회지
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• 제19권4호
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• pp.258-265
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• 1991

담자균효모 Leucosporidium scottii, Leucosporidium fellii, Leucosporidium lari-marini, Rhodosporidium fluviale의 ubiuqinone계를 고속액체크로마토그래피에 의해 결정하였다. Leucosporidium scottii 균주는 교배형 또는 self-sporulating 형에 관계없이 Q-9 또는 Q-10계를 가지고 있었다. 특히 동일 균주에서도 ubiquinone계의 변이가 관찰되었다. 이는 분류지표로서 중요시 되는 ubiquinone계의 재평가를 시사하는 새로운 사실로 간주된다. Leucosporidium fellii는 Q-9, Leucosporidium lari-marini는 Q-8, Rhodosporidium fuviale는 Q-10을 함유하고 있었다. L. lari-marini의 분류학적 위치는 다각적 연구에 기초하여 해명되어야 한다.

• 제어로봇시스템학회논문지
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• 제11권10호
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• pp.857-863
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• 2005

A yeast strain utilizing styrene epoxide as a sole carbon and energy source was isolated from soil samples for the production of enantiopure of styrene epoxide by kinetic resolution. The strain, identified as a Rhodosporidium toruloides SJ-4, expressed an epoxide hydrolase which preferentially converted (R)-styrene epoxide into the corresponding diol. A maximum activity of 135 U/L was observed when biomass (dry cell mass) reached 6.7 g/L at 21 h of batch culture. Under the partially optimized reaction conditions ($35^{\circ}C$ and pH 8.0), the optically pure (S)-styrene epoxide was obtained with the yield of 21% when the initial substrate concentration was 100 mM. The reaction was completed at 9 h.

• 생명과학회지
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• 제13권6호
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• pp.788-793
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• 2003

Rhodosporidium toruloides SJ-4의 epoxide hydrolase의 입체선택적 가수분해 반응을 이용하여 hollow-fiber 반응기에서 라세믹 phenyl oxirane 기질로부터 광학활성 phenyl oxirane을 생산하였다. 라세믹 에폭사이드 기질의 수용액 상에서의 낮은 용해도로 인한 저농도 반응의 문제점을 극복하기 위하여 dodecane 유기용매에 용해시켜 lumen 부위로 공급하였으며, 생촉매인 R. toruloides 세포 현탁액은 수용액강인 shell 부위에 위치시킴으로써 유기용매 사용에 따른 생촉매 활성 저하를 줄인 1단계 반응기 시스템에서는 200 mM의 고농도에서 (S)-phenyl oxirane을 생산할 수 있었다. 또한, 반응 산물로 생성되는 diol에 의한 생촉매 활성저해효과를 감소시키기 위하여 2단계 hollow-fiber 반응기에서는 완충용액을 이용하여 diol을 제거시킨 결과 300 mM에서 EH 활성을 이용한 입체선택적 가수분해반응을 수행할 수 있었으며, 200∼300 mM의 고농도 라세믹 기질로부터 99% ee 이상의 광학순도를 가진 (S)-phenyl oxirane을 이론 수율 대비 12∼35% 수율로 얻을 수 있었다.

• Journal of Microbiology and Biotechnology
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• 제27권10호
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• pp.1773-1777
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• 2017

The aim of this study was to examine the efficiency of Rhodosporidium toruloides as a new tool to evaluate the triglyceride (TG) reduction effects of anti-obesity candidate materials. Unfermented and fermented persimmon leaf hot water extracts (UFPLE and FPLE) were used as anti-obesity agents. The content of TG in R. toruloides treated with FPLE was less than those with UFPLE by about 11% (p < 0.05) relative to the control (R. toruloides incubated in YPD medium without the agents). Fat reduction in 3T3-L1 cells achieved by FPLE was about 13% higher than that achieved by UFPLE.

• 한국미생물·생명공학회지
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• 제24권6호
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• pp.641-646
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• 1996

[$\gamma$-$^{32}$P]ATP was used to test phosphorylation of membrane proteins of mating type a cells of heterobasidiomycetous yeast Rhodosporidium toruloides separated by non-denaturing electrophoresis. The phosphoprotein was observed in the membrane proteins. The phosphorylation was inhibited by the pheromone rhodotorucine A (Rh. A) secreted by mating type A of the yeast. Rh. A didn't inhibit the phosphorylation in the presence of a trigger peptidase (TPase) inhibitor, antipain. Partially digested Rh. A by trypsin maintained the phosphorylation inhibitory activity. These results show that TPase activity plays an important role in the transduction of pheromone signal in the yeast.

• Biotechnology and Bioprocess Engineering:BBE
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• 제8권5호
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• pp.306-308
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• 2003

Enantioselective hydrolysis for the production of chiral styrene oxide was investigated using the epoxide hydrolase activity of a newly isolated Rhodosporidium kratochvilovae SYU-08. The effects of reaction parameters - buffer type, pH, temperature, initial substrate concentrations, phenyl-1,2-ethanediol concentrations on hydrolysis rate, and enantioselectivity - were analyzed. Optically active (S)-styrene oxide with an enantiomeric excess higher than 99 % was obtained from its racemate. with a yield of 38 % (theoretically 50% maximum yield) from an initial concentration of 80 mM.

• 한국식품영양과학회지
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• 제26권6호
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• pp.1246-1251
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• 1997

When the membrane protein fraction of mating type a cells of heterobasidiomycetous yeast R. toruloides was phosphorylated in vitro, two phosphorylated proteins of 72Kd and 57Kd were detected on SDS-polyacryamide gel. The phosphorylation reaction was inhibited by rhodotorucine A(Rh. A) which is a sexual pheromone secreted by mating type A cells. The inhibition of phosphorylation by Rh. A was dependent on $Ca^{2+}$, and independent on $Mg^{2+}$ or calmodulin. When adding trigger peptidase(TPase) inhibitor, antipain, no inhibition of phosphory was observed. Also, by adding the trysin-digested product of Rh. A, the phosphorylation was inhibited as the action of Rh. A. From these results, it is expected that the inhibition of membrane protein phosphorylation should be caused by the digested product of Rh. A with TPase.