Project/Area Number |
02102006
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Research Category |
Grant-in-Aid for Specially Promoted Research
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Allocation Type | Single-year Grants |
Research Institution | KYUSHU UNIVERSITY |
Principal Investigator |
MURAKAMI Yukito Kyushu University, Institute for Fundamental Research in Organic Chemistry, Professor, 有機化学基礎研究センター, 教授 (30037717)
|
Co-Investigator(Kenkyū-buntansha) |
TAKAGI Makoto Kyushu University, Faculty of Engineering, Professor, 工学部, 教授 (90037739)
KIKUCHI Jun-ichi Kyushu University, Insitute for Fundamental Research in Organic Chemistry, Assoc, 有機化学基礎研究センター, 助教授 (90153056)
OHNO Teruhisa Kyushu University, Faculty of Engineering, Associate Professor, 工学部, 助教授 (10203887)
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Project Period (FY) |
1990 – 1993
|
Project Status |
Completed (Fiscal Year 1993)
|
Budget Amount *help |
¥205,000,000 (Direct Cost: ¥205,000,000)
Fiscal Year 1993: ¥15,000,000 (Direct Cost: ¥15,000,000)
Fiscal Year 1992: ¥50,000,000 (Direct Cost: ¥50,000,000)
Fiscal Year 1991: ¥50,000,000 (Direct Cost: ¥50,000,000)
Fiscal Year 1990: ¥90,000,000 (Direct Cost: ¥90,000,000)
|
Keywords | artificial enzyme / artificial receptor / bilayr membrane / hydrophobic vitaminB_6 / hydrophobic vitaminB_<12> / DNA / cyclophane / supramolecular effect / 疎水性ビタミンB_6 / 疎水性ビタミンB_<12> / シロクロファン / 分子認識 / 人工レセプタ- / タコ型シクロファン / かご型シクロファン / ビタミンB_6 / ビタミンB_<12> / 合成脂質 / 異性化反応 |
Research Abstract |
1. The following artificial receptors, which are capable of controlling catalytic activities of artificial enzymes, were designed and synthesized : octopus cyclophanes having the induced-fit function, cage-type cyclophanes being recognizable guest molecules through the lock-and-key mechanism, steroid cyclophanes having intermediate character between these structual types of hosts, hexapus cyclophanes as enterobactin models, and functionalized DNA-intercalators. 2. These artificial receptors perform as efficient intracellular receptors in aqueous solutions, reflecting the individual molecular characteristics. In addition, these receptors act as effective cell-surface receptors, when embedded in bilayr membranes formed with synthetic peptide lipids. Especially, a chiral cage-type cyclophane incorporated in a bilayr membrane exhibits chiral recognition behavior toward hydrophobic amino acids, the substrates for artificial enzymes. 3. The artificial vitaminB_6enzymes, each constituted with a bilayr-forming peptide lipid, hydrophobic vitaminB_6derivative, and metal ions, show catalytic performance as transaminase, tryptophan synthase, and aldolase under mild conditions in aqueous media to mediate stereospecific transformation of amino acids. 4. The artificial vitaminB_<12>enzymes, each formed with a hydrophobic vitaminB_<12>derivative and a bilayr-forming lipid, exhibit catalytic functions as methylmalonyl-CoA mutase, glutamate mutase, and alpha-methyleneglutarate mutase. By combination of the artificial enzyme with a co-catalyst capable of activating the substrates, the isomerization reactions accompanied with the carbon-skeleton rearrangement proceed with turnover of the artificial enzyme. 5. A bilayr-type artificial vitaminB_6enzyme having a transaminase activity and a bilayr-type artificial vitaminB_<12>enzyme having a glutamate mutase activity can be interconnected to perform the respective reactions successively.
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