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Determination of dihydroxyacetone and glycerol in fermentation broth by pyrolytic methylation/gas chromatography

机译:裂解甲基化/气相色谱法测定发酵液中的二羟基丙酮和甘油

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A method to determine dihydroxyacetone (DHA)and glycerol in fermentation broth was developed on the basis of pyrolytic methylation-gas chromatography (GC)using a vertical microfurnace pyrolyzer.With the on-line pyrolytic methylation in the presence of an organic alkali, tetram-ethylammonium hydroxide ((CH_3)_4NOH, TMAH), DHA and glycerol were converted into their corresponding methyl ethers.Thus, fermentation broth samples containing DHA and glycerol could be well determined simultaneously by this pyrolytic methylation-GC without using any pre-treatment procedures.Important factors such as reaction temperature, the amount of TMAH to DHA and glycerol were investigated in order to obtain the optimum methylation conditions.Thus, obtained results showed that 0.4 mul 25% TMAH aqueous solution at 400 deg C enabled the highly sensitive determination of DHA and glycerol contained in 0.2 mul aqueous samples.The achieved calibration curves exhibit good linearity with regression coefficients of 0.996 and 0.998 for DHA and gelycerol at the concentration range from 1 to 100 g/l, respectively.The precision was quite high with the R.S.D.within 5.0% for DHA at 30g/l and glycerol at 15 g/l concentration levels, and the limit of detection reached 0.016g/l.The potential of the proposed method was assessed by applying it to determination of both the analytes in fermentation broth during the bioconversion of glycerol to DHA by Acetobacteria sp.The results proved that this on-line pyrolytic methylation-GC technique was a rapid, convenient and highly sensitive method for monitoring the bioprocesses of DHA.
机译:在立式微炉热解器的热解甲基化-气相色谱(GC)的基础上,建立了测定发酵液中二羟基丙酮(DHA)和甘油的方法。将乙基氢氧化铵((CH_3)_4NOH,TMAH),DHA和甘油转化为相应的甲基醚,因此无需进行任何预处理,即可通过该热解甲基化GC同时测定含DHA和甘油的发酵液样品。为了获得最佳的甲基化条件,研究了反应温度,TMAH对DHA的量和甘油等重要因素,从而获得的结果表明,0.4 mul 25%TMAH水溶液在400℃下可以实现高灵敏度的DHA测定。样品中所含的甘油和甘油含量为0.2 mul。所获得的校准曲线具有良好的线性,回归系数为0 DHA和甘油的浓度范围为1至100 g / l分别为0.996和0.998.RSD的精密度非常高,当DHA浓度为30g / l时甘油含量为5.0%,甘油浓度为15 g / l时甘油含量为5.0%。检出限为0.016g / l。该方法可用于醋杆菌法将甘油生物转化为DHA的过程中测定发酵液中两种分析物的潜力。结果证明了该在线热解法的可行性。甲基化-GC技术是一种快速,方便且高度灵敏的监测DHA生物过程的方法。

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