Doull J, Ahmed Z, Stuttard C, Vining L C
J Gen Microbiol. 1985 Jan;131(1):97-104. doi: 10.1099/00221287-131-1-97.
Twelve Streptomyces venezuelae mutants blocked in chloramphenicol biosynthesis were isolated. Two of these (Cm1-1 and Cm1-12) were apparently blocked in the conversion of chorismic acid to p-aminophenylalanine and three (Cm1-4, Cm1-5 and Cm1-8) accumulated p-aminophenylalanine and may have been blocked in the hydroxylation reaction that converted this intermediate to p-aminophenylserine. One mutant (Cm1-2) accumulated D-threo-1-p-nitrophenyl-2-propionamido-1,3-propanediol and D-threo-1-p-nitrophenyl-2-isobutyramido-1,3-propanediol, indicating that chlorination of the alpha-N-acyl group of chloramphenicol was blocked. The remaining six strains did not excrete any detectable chloramphenicol pathway intermediates.
分离出了12株在氯霉素生物合成过程中受阻的委内瑞拉链霉菌突变体。其中两株(Cm1-1和Cm1-12)显然在分支酸转化为对氨基苯丙氨酸的过程中受阻,三株(Cm1-4、Cm1-5和Cm1-8)积累了对氨基苯丙氨酸,可能在将该中间体转化为对氨基苯丝氨酸的羟基化反应中受阻。一个突变体(Cm1-2)积累了D-苏式-1-对硝基苯基-2-丙酰胺基-1,3-丙二醇和D-苏式-1-对硝基苯基-2-异丁酰胺基-1,3-丙二醇,表明氯霉素α-N-酰基的氯化受阻。其余六株菌株没有分泌任何可检测到的氯霉素途径中间体。