Darling Marine Center, University of Maine, Walpole, Maine 04573.
Appl Environ Microbiol. 1991 Dec;57(12):3476-81. doi: 10.1128/aem.57.12.3476-3481.1991.
Acetate concentrations in marine and freshwater matrices were measured by an enzymatic technique which coupled the synthesis of acetyl coenzyme A to AMP production. The resulting AMP was assayed by a sensitive and relatively rapid high-pressure liquid chromatography method, using an aqueous, isocratic mobile phase for elution. The method was insensitive to the presence of seawater salts and required no sample prepurification or distillation. Propionate caused a minor, but statistically insignificant, interference when equimolar with acetate; butyrate caused no interference, even at relatively high concentrations. Detection limits for acetate were approximately 100 nM with a precision of about 5%. Pore waters from two intertidal sediments contained approximately 1 to 12 muM acetate; the concentrations were linearly but inversely correlated with porewater sulfate.
采用一种酶促技术来测量海洋和淡水基质中的醋酸盐浓度,该技术将乙酰辅酶 A 的合成与 AMP 的生成偶联起来。所得的 AMP 通过一种灵敏且相对快速的高压液相色谱法进行测定,使用水相、等度流动相进行洗脱。该方法对海水盐的存在不敏感,并且不需要样品预纯化或蒸馏。丙酸与醋酸盐等摩尔存在时会引起轻微但无统计学意义的干扰;而丁酸即使在较高浓度下也不会造成干扰。醋酸盐的检测限约为 100 nM,精密度约为 5%。两个潮间带沉积物的孔隙水中含有约 1 至 12 μM 的醋酸盐;这些浓度与孔隙水中的硫酸盐呈线性反比关系。