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首页> 外文期刊>International Journal of African and Asian Studies >Biosynthesis of Deuterium Labeled Phenylalanine. Facultative Methylotrophic Bacterium ?revibacterium Methylicum # 5662 with RuMP Cycle of Carbon Assimilation
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Biosynthesis of Deuterium Labeled Phenylalanine. Facultative Methylotrophic Bacterium ?revibacterium Methylicum # 5662 with RuMP Cycle of Carbon Assimilation

机译:氘标记的苯丙氨酸的生物合成。具有碳同化RuMP循环的兼性甲基营养型细菌亚甲基杆菌#5662

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We used Gram-positive aerobic facultative methylotrophic bacterium, Brevibacterium methylicum, L-phenylalanine producer with ribulose-5-monophosphate (RuMP) cycle for carbon assimilation for microbiological preparation of [2H]phenylalanine via conversion of low molecular weight substrates ([U-2H]MeOH and 2H2O). For this purpose, the cells of the methylotroph with improved growth characteristics were used on minimal salt media M9 supplemented with 2% (v/v) [U-2H]MeOH and increasing gradient of 2?2O concentration from 0; 24.5; 49.0; 73.5 up to 98% (v/v) 2?2O. L-phenylalanine was isolated from the growth medium after adding 5 M 2HCl (in 2?2?), pH = 2.0 by extraction with isopropanol and subsequent crystallization in ethanol (output 0.65 g/l). Alanine, valine, and leucine/isoleucine were produced and accumulated exogenously in amounts of 5–6 mmol in addition to the main product of biosynthesis. The method allows to obtain [2?]amino acids with different levels of deuterium enrichment, depending on 2?2O concentration in growth media, from 17% 2? (2 deuterium atoms) (on the growth medium with 24.5% (v/v) 2?2?) up to 75% 2? (6 deuterium atoms) (on the growth medium with 98% (v/v) 2?2?) with introduction of deuterium to benzyl ?6?5??2-fragment of molecule that is confirmed with the data of electron impact (EI) mass spectrometry analysis of methyl ethers of N-5-dimethylamino(naphthalene)-1-sulfochloride [2H]amino acids after the separation by reverse-phase HPLC. Keywords: Brevibacterium methylicum, [U-2H]MeOH, heavy water, biosynthesis, [2H]amino acids, EI mass spectrometry, HPLC.
机译:我们使用革兰氏阳性需氧兼性甲基营养细菌,甲基短杆菌,L-苯丙氨酸生产者与核糖5-单磷酸(RuMP)循环进行碳同化,以通过低分子量底物([U-2H [MeOH和2H2O)。为此,将具有改善生长特性的甲基营养菌的细胞用于补充了2%(v / v)[U-2H] MeOH和从0开始增加2?2O浓度梯度的最小盐培养基M9上。 24.5; 49.0; 73.5至98%(v / v)2?2O。加入异丙醇萃取,然后在乙醇中结晶(输出0.65 g / l),加入5 M 2HCl(在2?2?中),pH = 2.0,从生长培养基中分离出L-苯丙氨酸。除生物合成的主要产物外,丙氨酸,缬氨酸和亮氨酸/异亮氨酸的产生和积累量为5-6 mmol。该方法允许从17%的2%氨基酸中获得[2 ^]具有不同水平的氘富集的[2 ^]氨基酸,这取决于生长培养基中的2 ^ 2O浓度。 (2个氘原子)(在生长培养基中为24.5%(v / v)2?2?)高达75%2?。 (6个氘原子)(在98%(v / v)2?2?的生长培养基上),并将氘引入分子的苄基?6?5?2 2-片段中,这已通过电子碰撞数据得到证实(反相HPLC分离后,N-5-二甲基氨基(萘)-1-硫氯化物[2H]氨基酸的甲基醚的EI)质谱分析。关键词:甲基短杆菌,[U-2H] MeOH,重水,生物合成,[2H]氨基酸,EI质谱,HPLC。

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