HOECHST AG, 6230 Frankfurt/M. 80, and Institut für Bodenbiologie, Bundesforschungsanstalt für Landwirtschaft, 3300 Braunschweig, Federal Republic of Germany.
Appl Environ Microbiol. 1989 Mar;55(3):711-6. doi: 10.1128/aem.55.3.711-716.1989.
Three hundred bacterial isolates from soil were tested for resistance against phosphinothricin [PPT; dl-homoalanin-4-yl(methyl)phosphinic acid], the active ingredient of the herbicide BASTA. Eight resistant bacterial strains and Escherichia coli were analyzed for PPT-transforming activities. At least three different enzymatic reactions could be detected in cell extracts. In six strains an acetyltransferase was active, synthesizing N-acetyl-PPT in the presence of PPT and acetyl coenzyme A. All strains could degrade PPT to its corresponding 2-oxoacid {2-oxo-4-[(hydroxy)(methyl)phosphinoyl] butyric acid} by transamination. Rhodococcus sp., the only tested strain that was able to utilize PPT as a sole source of nitrogen, formed 2-oxo-4[(hydroxy)(methyl)phosphinoyl]butyric acid by oxidative deamination. This enzymatic activity was inducible by l-glutamic acid or PPT itself but not in the presence of NH(4). d-PPT transformation was not detectable in any of the investigated strains.
从土壤中分离出的 300 株细菌被测试对草丁膦(PPT;DL-高丙氨酸-4-基(甲基)膦酸)的抗性,草丁膦是除草剂巴斯塔的活性成分。对 8 株抗性细菌株和大肠杆菌进行了 PPT 转化活性分析。在细胞提取物中至少可以检测到三种不同的酶反应。在 6 株菌中,乙酰转移酶具有活性,在存在 PPT 和乙酰辅酶 A 的情况下合成 N-乙酰-PPT。所有菌株都可以通过转氨基作用将 PPT 降解为其相应的 2-氧代酸{2-氧代-4-[(羟基)(甲基)膦酰基]丁酸}。红球菌属是唯一被测试的能够将 PPT 作为唯一氮源利用的菌株,通过氧化脱氨作用形成 2-氧代-4-[(羟基)(甲基)膦酰基]丁酸。这种酶活性可被 L-谷氨酸或 PPT 本身诱导,但不能在 NH4存在的情况下诱导。在所有研究的菌株中都无法检测到 d-PPT 的转化。