반응 #2006456

ord-de809c94e52644a19f2bc432f30824a5

반응 방정식

[Na+].[OH-]
sodium hydroxide
COc1ccc(CC(C)=O)cc1
1-(4-methoxyphenyl)-2-propanone
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
D-glucose
NC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)c1
NAD+
C[C@@H](N)C(=O)O
D-alanine
Cc1ncc(COP(=O)(O)O)c(C=O)c1O
pyridoxal phosphate
COc1ccc(CC(C)N)cc1
1-(4-methoxyphenyl)-2-aminopropane

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타(pNTASPAG), obtained in Example 11, which
  2. 2
    workup.ADDITIONwere added
  3. 3
    기타During the reaction
  4. 4
    기타the reaction liquid
  5. 5
    workup.ALIQUOTwas sampled
  6. 6
    추출From the sample, 1-(4-methoxyphenyl)-2-aminopropane was extracted by the addition of ethyl acetate

실험 절차

To a flask containing 1.5 g of a substrate 1-(4-methoxyphenyl)-2-propanone, 4.94 g of D-glucose, 6.1 mg of NAD+, 4.88 g of D-alanine, and 4.0 mg of pyridoxal phosphate, 30 ml of a culture fluid of the E. coli HB101 (pNTASPAG), obtained in Example 11, which expresses TAS, PALDH, and GDH were added. The resultant product was stirred at 30° C. while being adjusted to a pH of 6.8 by drippage of 5 N aqueous solution of sodium hydroxide. During the reaction, the reaction liquid was sampled. From the sample, 1-(4-methoxyphenyl)-2-aminopropane was extracted by the addition of ethyl acetate after basifying the sample with 6 N aqueous solution of sodium hydroxide. The amount of 1-(4-methoxyphenyl)-2-aminopropane produced was measured by analyzing 1-(4-methoxyphenyl)-2-aminopropane under the following HPLC conditions. Further, by the law of the art, 1-(4-methoxyphenyl)-2-aminopropane thus obtained was acted on by 3,5-dinitrobenzyl chloride to form a dinitrobenzyl derivative. After that, the dinitrobenzyl derivative was analyzed under the following HPLC conditions, whereby the optical purity thereof was measured.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08168412B2uspto-grants-2012_05