• 제목/요약/키워드: acceptor reaction

검색결과 160건 처리시간 0.033초

Kinetic Studies on the Reaction of the Heterobimetallic Anion, $(OC)_5CrMn(CO)_5{^-}M^+\;(M^+=Na^+,\;PPN^+)$ with Allyl Bromide

  • Park, Yong K.;Kim, Gyu S.;Song, Gwan O.
    • Bulletin of the Korean Chemical Society
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    • 제16권4호
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    • pp.310-315
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    • 1995
  • The heterobimetallic anion, (OC)5CrMn(CO)5-M+ (M+=Na+, PPN+), which has a donor-acceptor metal-metal bond1, was reacted with allyl bromide to yield BrCr(CO)5- and Mn(CO)5(CH2CHCH2). The reaction mechanism has been proposed in terms of the consecutive reaction pathway in which Cr(CO)5(THF) is an important intermediate leading to the corresponding product. Counterion effect on this reaction was also evaluated and the results were compared with those of the corresponding reaction of the mononuclear carbonyl anion, Mn(CO)5-.

Production of Glucooligosaccharides and Mannitol from Leuconostoc mesenteroides B-742 Fermentation and its Separation from Byproducts

  • Chung Chang-Ho
    • Journal of Microbiology and Biotechnology
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    • 제16권2호
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    • pp.325-329
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    • 2006
  • Leuconostoc mesenteroides B-742 fermentations with maltose as an acceptor were tested for glucooligosaccharides and mannitol co-production. Leuconostoc oligosaccharides were produced that were oligomers with a size range of DP 2 to 7 and were primarily DP 3, 4, 5, and 6, containing mainly ${\alpha}-1,4$ and ${\alpha}-1,6$ linkages. Maltose was linked to the reducing end of the isomaltosyl residues. The $Ca^{2+}$ form of cation-exchange column could separate glucooligosaccharides from byproducts.

전분으로부터 Amyloglucosidase의 당전이반응에 의한 배당체의 합성 (Synthesis of Glycoside by Transglycosylation of Amyloglucosidase from Starch.)

  • 박종이;이희정;이태호
    • 한국미생물·생명공학회지
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    • 제26권2호
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    • pp.187-194
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    • 1998
  • 수계에서 전분 가수분해효소의 transglycosylation반응을 이용하여 배당체(glycoside)를 합성하였다. Glycosyl donor인 starch와 glycosyl acceptor인 benzylalcohol을 반응기질로 선택하였다. 시판되는 9종의 당가수분해효소의 transglycosylation활성을 조사한 결과 glucose와 한 종류의 glycoside만을 생산하는 amyloglucosidase(from Rhizopus sp.)를 반응효소로 선정하였다. Amyloglucosidase에 의해 합성된 배당체는 여러 가지 분석을 통해 glucose의 1번 OH기에 benzylalcohol이 ${alpha}$형태로 결합된 benzylalcohol-${alpha}$-glucoside(BG)임을 확인하였다. 수계에서 이 효소에 의한 transglycosylation 반응의 최적조건은 starch 50mg/$m\ell$, benzylalcohol 50 mg/ml, 온도 45$^{\circ}C$, 효소량 10 unit/ml, pH 5.0, 반응시간 32시간이었으며 합성된 BG는 amyloglucosidase에 의해서는 분해되지 않았고 ${alpha}$-glucosidase에 의해 glucose와 benzylalcohol로 가수분해되었다.

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Direct Electrode Reaction of Fe(III)-Reducing Bacterium, Shewanella putrefaciens

  • Kim, Byung-Hong;Kim, Hyung-Joo;Hyun, Moon-Sik;Park, Doo-Hyun
    • Journal of Microbiology and Biotechnology
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    • 제9권2호
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    • pp.127-131
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    • 1999
  • Anaerobically grown cells of an Fe(III)-reducing bacterium, Shewanella putrefaciens IR-l, were electrochemically active with an apparent reduction potential of about 0.15 V against a saturated calomel electrode in the cyclic voltammetry. The bacterium did not grow fermentatively on lactate, but grew in an anode compartment of a three-electrode electrochemical cell using lactate as an electron donor and the electrode as the electron acceptor. This property was shared by a large number of Fe(III)-reducing bacterial isolates. This is the first observation of a direct electrochemical reaction by an intact bacterial cell, which is believed to be possible due to the electron carrier(s) located at the cell surface involved in the reduction of the natural water insoluble electron acceptor, Fe(III).

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New Design and Synthesis of Donor-Acceptor units by Introducing Boron Based to Non-Boron based Semiconductor for high Voc OPV

  • Ryu, Ka Yeon;Cho, Kyuwan;Kim, Won-Suk;Kim, Kyungkon
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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    • pp.432.2-432.2
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    • 2016
  • A new A-D-A type (Acceptor-Donor-Acceptor) conjugated based on pyridine-borane complex (Donor), non-boron fluorine (Donor) and 2,5-bis(alkyl)-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (DPP) (Acceptor) were designed and synthesized via Pd-catalyzed Suzuki cross-coupling reaction. The synthesized boron based complex exhibited high electron affinity, which indicates deep HOMO energy levels and good visible absorption led to their use as donors in BHJ (bulk heterojunction) solar cells. Inverted devices were fabricated, reaching open-circuit voltage as high as 0.91eV. To probe structure-property relationship and search for design principle, we have synthesized pyridine-boron based electron donating small molecules. In this study, we report a new synthetic approach, molecular structure, charge carrier mobility and morphology of blended film and their correlation with the photovoltaic J-V characteristics in details.

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Leuconostoc mesenteroides NRRL B-1149의 Sucrose phosohorylase의 분리와 특성 연구 (Purification and Characterization Sucrose phosohorylase in Leuconostoc mesenteroides NRRL B-1149)

  • 이진하;박준성;박현정;조재영;최정식;김도만
    • KSBB Journal
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    • 제19권5호
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    • pp.363-367
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    • 2004
  • Leuconostoc mesenteroides NRRL B-1149 produces various glucoseyltransferases for the synthesis of dextran, levan and glucose-1-phosphate using sucrose as a substrate. A sucrose phosphorylase (1149SPase) was purified from L. mesenteroides NRRL B-1149 culture by using hollow fiber filtration (30 kDa cut off), Toyopearl DEAE 650 M column chromatography and following two times of DEAE-Sepharose column chromatographies. The specific activity of the purified 1149SPase was 25.7 (U/mg) with $16\%$ yield. The 1149SPase showed a molecular size of 56 kDa on denatured $10\%$ SDS-PAGE. The N-terminal amino acid sequence of the enzyme was MEIQNKAM. The optimum pH and temperature of this enzyme were 6.2~6.5 and 37^{circ}C, respectively. It had an apparent K_{m} of 6.0 mM and K_{cat} of 1.62/s for sucrose. 1149SPase crystal was formed by hanging drop diffusion technique using 20 mM calcium chloride dihydrate, 100 mM sodium acetate trihydrate pH 4.6 and $30\%$ 2-methyl-2,4-pentanediol as vaporizing and reservation solution. The 1149SPase catalyzes transferring of glucose from isomaltose or sucrose to salicin and salicyl alcohol by disproportionation reaction or acceptor reaction and synthesized two acceptor products, respectively.

Simultaneous Biocatalytic Synthesis of Panose During Lactate Fermentation in Kimchi

  • Han, Nam-Soo;Jung, Yoon-Seung;Eom, Hyun-Ju;Koh, Young-Ho;Robyt, John F.;Seo, Jin-Ho
    • Journal of Microbiology and Biotechnology
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    • 제12권1호
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    • pp.46-52
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    • 2002
  • As a functional additive for intestinal microflora, panose ($6^2-{\alpha}$-D-glucopyranosylmaltose) was synthesized during kimchi fermentation using the glucose transferring reaction of glucansucrase from Leuconostoc mesenteroides. For the glucose transferring reaction, sucrose and maltose were added ($2\%$ each, w/v) to dongchimi-kimchi as the glucosyl donor and acceptor molecule, respectively. After five days of incubation at $10^{\circ}C$, referring to the initial phase for the production of lactic acid in kimchi, over $60\%$ (w/v) of the total sugars were converted into panose and other branched oligosaccharides. Thereafter, the kimchi was stored at $4^{\circ}C$ and the amount of panose remained at a constant level for three weeks, thereby indicating the stability of panose to microbial degradation during the period of kimchi consumption. The use of maltose as the acceptor molecule in the kimchi also facilitated a lower viscosity in the kimchi-juice by preventing the synthesis of a dextran-like polymer which caused an unfavorable taste. Accordingly, the application of this new method of simultaneous biocatalytic synthesis of oligosaccharides during lactate fermentation should facilitate the extensive development of new function-added lactate foods.