详细信息

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

文献类型:期刊文献

中文题名:酶法合成抗癌新药氟铁龙前体——5-FUR

英文题名:Enzymatic Synthesis of 5-FUR, a Precursor of a New Anti-cancer Medicine 5'-DFUR

作者:闫蓬勃[1];丁庆豹[1];邱蔚然[1];严滢[1];石佳瑛[1]

机构:[1]华东理工大学生物反应器工程国家重点实验室,上海200237

年份:2001

卷号:27

期号:2

起止页码:143

中文期刊名:华东理工大学学报(自然科学版)

外文期刊名:Journal of East China University of Science and Technology

收录:CSTPCD;;Scopus;北大核心:【北大核心2000】;CSCD:【CSCD2011_2012】;

语种:中文

中文关键词:酶法合成;5-氟尿苷;乙酰短杆菌;5-氟尿嘧啶;鸟苷;抗癌药物

外文关键词:enzymatic synthesis; 5 fluorouridine; Brevibacterium acetylicum; 5 fluorouracil; guanosine

摘要:筛选得到一株核苷磷酸化酶活力高的乙酰短杆菌 ,以该菌体为酶源酶法合成抗癌新药氟铁龙前体 5-氟尿苷 ,所用反应物为鸟苷和 5-氟尿嘧啶。在 1 50 m L的摇瓶装液 1 5m L的条件下进行研究 ,结果显示 :菌体添加量 2 0~ 30 g/L,底物浓度 1 0 0 mmol/L,磷酸盐浓度 50 mmol/L( p H8.0 ) ,60°C,摇床转速 1 60 r/min,反应 4h,5-氟尿苷的转化率可以达到 60
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.

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