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酶法合成抗癌新药氟铁龙前体——5-FUR

闫蓬勃 丁庆豹 邱蔚然 严滢 石佳瑛

华东理工大学学报(自然科学版)2001,Vol.27Issue(2):143-146,4.
华东理工大学学报(自然科学版)2001,Vol.27Issue(2):143-146,4.

酶法合成抗癌新药氟铁龙前体——5-FUR

Enzymatic Synthesis of 5-FUR, a Precursor of a New Anti-cancer Medicine 5-DFUR

闫蓬勃 1丁庆豹 1邱蔚然 1严滢 1石佳瑛1

作者信息

  • 1. 华东理工大学
  • 折叠

摘要

Abstract

A strain of Brevibacterium acetylium QDY2000 that can produce nucleoside phosphorylase has been successfully screened. 5-Fluorouridine which can be used as the precursor of the 5′-deoxy-5-fluorouridine was enzymatically synthesized from guanosine and 5-fluorouracil by QDY2000. The optimal reaction conditions were studied in 150mL shaking bottle with 15mL solution. The conversion yield could reach above 60% while the reaction mixtures, containing 20~30g/L wet cells, 100mmol/L substrates and 50mmol/L phosphate buffer (pH adjusted to 8.0 with NaOH), were incubated at 60°C for 4h at the shaking speed of 160r/min.

关键词

酶法合成/5-氟尿苷/乙酰短杆菌/5-氟尿嘧啶/鸟苷

分类

生物科学

引用本文复制引用

闫蓬勃,丁庆豹,邱蔚然,严滢,石佳瑛..酶法合成抗癌新药氟铁龙前体——5-FUR[J].华东理工大学学报(自然科学版),2001,27(2):143-146,4.

华东理工大学学报(自然科学版)

OA北大核心CSCD

1006-3080

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