• Journal of Microbiology and Biotechnology
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• 제23권4호
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• pp.473-482
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• 2013

The desulfurization ability of Sphingomonas subarctica T7b was evaluated using resting and immobilized cells with dibenzothiophene (DBT), alkyl DBTs, and commercial light gas oil (LGO) as the substrates. The resting cells of S. subarctica T7b degraded 239.2 mg of the initial 250 mg of DBT/l (1.36 mM) within 24 h at $27^{\circ}C$, while 127.5 mg of 2-hydroxybiphenyl (2-HBP)/l (0.75 mM) was formed, representing a 55% conversion of the DBT. The DBT desulfurization activity was significantly affected by the aqueous-to-oil phase ratio. In addition, the resting cells of S. subarctica T7b were able to desulfurize alkyl DBTs with long alkyl chains, although the desulfurization rate decreased with an increase in the total carbon number of the alkylated DBTs. LGO with a total sulfur content of 280 mg/l was desulfurized to 152 mg/l after 24 h of reaction. Cells immobilized by entrapment with polyvinyl alcohol (PVA) exhibited a high DBT desulfurization activity, including repeated use for more than 8 batch cycles without loss of biodesulfurization activity. The stability of the immobilized cells was better than that of the resting cells at different initial pHs, higher temperatures, and for DBT biodesulfurization in successive degradation cycles. The immobilized cells were also easily separated from the oil and water phases, giving this method great potential for oil biodesulfurization.

• Journal of Microbiology and Biotechnology
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• 제7권5호
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• pp.345-351
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• 1997

An aqueous/organic two-phase reaction system was applied to the production of catechol using immobilized resting cells of Pseudomonas putida CY 400. Water/ethyl ether system was used because of high partition coefficient of catechol and thus to reduce the product inhibition and degradation. Among the tested immobilization carriers, polyacrylamide gel gave the highest catechol productivity. The immobilization seemed to protect the cells against solvent toxicity. From the simulation of reaction conditions based on two-phase models, it was found that there was an optimum acetate concentration at fixed benzoate and cell concentrations for the catechol productivity. A lower phase volume ratio (lower fraction of organic phase) gave a higher productivity. However, the substrate conversion was low at low phase volume ratio.

• Applied Biological Chemistry
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• 제38권1호
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• pp.1-6
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• 1995

Rhodocyclus gelatinosus KUP-74의 고농도 휴지균체로부터 ${\delta}-aminolevulinate$(ALA)를 연속적으로 생산하기 위한 최적조건을 검토하였다. 균체외 ALA양은 20 mg cells/ml의 균체농도까지는 농도 증가에 따른 rectangular hyperbola의 증가양식을 보였으나, 그 이상의 균체농도는 ALA 생산에 전혀 증가효과를 보이지 않았다. 20 mg cells/ml의 반응계에서, 균체외 ALA의 효과적 생산을 위한 첨가물질의 최저농도는 levulinate 4 mM과 L-glutamate 5 mM로 나타났으며, 배양 3시간후 ALA 양의 최대치를 보였다. 한편, Ca-alginate를 이용한 포괄법으로 고정화시킨 균체로부터 효과적으로 ALA를 생산하기 위한 첨가물질의 최적농도는 levulinate 6 mM과 L-glutamate 10 mM로 나타났으며, 배양 6시간째에 균체외 ALA 양의 최대치를 보였다. 또한, 이 조건 하에서 고정화균체와 고농도의 휴지균체에 의한 ALA의 연속생산성을 검토한 결과, 이들 균체에 의한 50% ALA 생산성은 각각 185시간과 100시간에서 나타났으며, 생산된 균체외 ALA의 회수를 위해서는 균체를 고정화시키는 방법이 효과적이었다.

• 한국미생물·생명공학회지
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• 제25권1호
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• pp.68-74
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• 1997

The conversion of D-sorbitol to L-sorbose by Gluconobater suboxydans was analyzed, and continuous production of L-sorbose was carried out in immobilized cell reactors. L-Sorbose production by high densities of resting cells was more effective than by conventional batch fermentations. Sorbitol dehydrogenase, an enzyme converting D-sorbitol to L-sorbose, did not suffer from substrate inhibition, but from product inhibition. When L-sorbose production was carried out with Ca-alginate-immobilized cells, about 60 g/l of L-sorbose was obtained. On the other hand, when the corn steep liquor (CSL) concentration of medium was reduced to 0.08%, 80 g/l of L-sorbose was obtained. Outgrowth inside the immobilized carriers was thought to block the pores of the carriers so that substrate could not easily diffuse through the carriers. Continuous production of L-sorbose was well accomplished in a bubble column reactor, and 6. 5 g/l.h of productivity and 81.2% of yield were obtained at a substrate feeding rate of 0.08h$^{-1}$ under the optimum conditions with carrier volume of 55% and aeration rate of 3 vvm.

• Journal of Microbiology and Biotechnology
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• 제13권5호
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• pp.687-691
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• 2003

Whole-cell immobilization of the hydrocarbon rich microalgae, Botryococcus braunii and B. protuberans, in alginate beads under air-lift batch cultures resulted in a significant increase in chlorophyll, carotenoid, dry weight, and 1ipid contents at stationary and resting growth phases, as compared to free cells. Photosynthetic activity in both the species, of Botryococcus was enhanced, relative to free cells, at any growth phase of cultures. Immobilization exerted a protective influence on ageing of the cultures as reflected by higher chlorophyll and dry weight contents. Entrapment also stabilized the chlorophyll and carotenoid contents even at stationary and resting phases as compared to free cells in both the species.

• 생명과학회지
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• 제17권12호
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• pp.1641-1648
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• 2007

Yippee 패밀리를 구성하는 yippee-유사 단백질들은 한 개의 zinc-finger 도메인을 지닌 Drosophila yippee 단백질의 homolog로서 모든 진핵생물에 존재하는 것으로 알려졌으나 그 기능은 밝혀진 바가 없다. 인체 T 림프구의 활성화과정 중 발현수준이 변화하는 유전자들을 선별하기 위해 인체 말초혈액에서 분리한 resting T 세포, immobilized anti-CD3에 의해 26시간 혹은 30시간 동안 활성화시킨 T 세포로부터 각각 정제한 total RNA를 이용하여 ODD-PCR을 수행한 결과, resting T 세포에서는 발현되지만 immobilized anti-CD3 활성화에 의해 세포주기를 개시하여 $G_1/S$ boundary에 도달한 T 세포들로부터는 전혀 발현되지 않는 흥미로운 유전자로서 Drosophila yippee 단백질 유전자의 인체 homolog인 YPEL5 유전자를 분리하였다. 노던 블로팅법으로 T 세포 활성화에 뒤이은 YPEL5 mRNA의 발현 변화를 조사한 결과, ${\sim}2.2kb$ 크기의 YPEL5 mRNA는 resting T 세포를 비롯하여 immobilize anti-CD3에 의한 활성화 후 1.5시간까지는 확인되었으나 활성화 후 5시간 이후부터 48시간에 이르는 시간에는 전혀 확인되지 않았다. YPEL5 단백질을 GFP-fusion 단백질로서 인체 암세포주인 HeLa 세포에 transfection하여 발현시킨 결과, GFP-YPEL5 단백질이 모두 핵에 위치하는 것으로 나타나 YPEL5 단백질이 핵단백질임을 확인하였다. 또한 YPEL5의 기능을 규명하기 위해 YPEL5 발현벡터를 HeLa 세포에 transfection 하고 발현시켜 HeLa 세포의 증식에 미치는 YPEL5의 영향을 MTT assay로 분석한 결과, vector plasmid를 transfection시킨 대조구의 47% 수준으로 세포증식이 감소하는 것으로 나타났다. 이러한 결과들은 YPEL5 mRNA의 발현이 T 세포 수용체를 통한 T 세포 활성화의 초기단계에 현저히 감소됨을 보여주며, 또한 YPEL5가 핵단백질로서 세포증식에 대해 저해효과를 미칠 수 있음을 시사한다.