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首页> 外文期刊>Macromolecules >USE OF POLY(ETHYLENE GLYCOL)S TO REGULATE POLY(3-HYDROXYBUTYRATE) MOLECULAR WEIGHT DURING ALCALIGENES EUTROPHUS CULTIVATIONS
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USE OF POLY(ETHYLENE GLYCOL)S TO REGULATE POLY(3-HYDROXYBUTYRATE) MOLECULAR WEIGHT DURING ALCALIGENES EUTROPHUS CULTIVATIONS

机译:在化解嗜碱菌富营养化过程中使用聚乙二醇调节聚(3-羟基丁酸)分子重量

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The ability of poly(ethylene glycol)s, PEGs, to control poly(3-hydroxybutyrate), P3HB, molecular weight in a microbial fermentation polymerization process was studied using Alcaligenes eutrophus with fructose as the sole carbon source. PEGs varying in molecular weight and end group functionality were added to the cultivation medium subsequent to cell growth, and their effects on polymer formation were evaluated. In general, A. eutrophus showed substantial tolerance for PEGs. This was illustrated by similar viable cell concentrations for the medium without PEG, 10% (w/v) PEG-IO 000 and 2% PEG-800. Furthermore, detrimental effects on polymer yields were not observed for concentrations of 5% PEG-106 and 10% PEG-10 000. The greatest reductions in molecular weight were obtained when relatively low molecular weight PEG was added to the medium. PEG-106 was most effective in that only 0.25% was required to reduce the number average molecular weight (M(n)) by 74%. The largest decrease in P3HB M(n) (from 455 000 to 19 400) was observed by adding 10% PEG-106 to the medium. The largest change in P3HB M(n) per incremental addition of PEG occurred in the 0-1% PEG concentration range. Supplementing the incubation medium with the monomethoxy ether CH3O-PEG-OH-350 and PEG-300 resulted in almost identical molecular weight reductions. However, the dimethoxy ether of tetraethylene glycol was not an effective agent for molecular weight reduction. Therefore, interaction between PEG and the PHA production system leading to molecular weight reduction was enhanced for lower molecular weight PEGs and required at least one PEG chain end functionality which may be a hydroxyl group. It is believed that PEG interacts with the A. eutrophus synthase in such a way to increase the rate of chain termination by water relative to chain propagation reactions. [References: 38]
机译:以果糖为唯一碳源的常绿胡芦巴,研究了聚乙二醇(PEG)在微生物发酵聚合过程中控制聚(3-羟基丁酸酯),P3HB分子量的能力。在细胞生长后,将分子量和端基官能度不同的PEG添加到培养基中,并评估它们对聚合物形成的影响。总体而言,真金曲霉显示出对PEG的实质耐受性。对于不含PEG,10%(w / v)PEG-10 000和2%PEG-800的培养基,类似的活细胞浓度可以说明这一点。此外,对于浓度为5%PEG-106和PEG-10 000的PEG,未观察到对聚合物收率的不利影响。当将相对低分子量的PEG添加到培养基中时,分子量的降低最大。 PEG-106最有效的地方在于,仅需0.25%的分子量即可将数均分子量(M(n))降低74%。通过向培养基中添加10%PEG-106,可以观察到P3HB M(n)的最大下降(从455 000下降到19 400)。每次递增添加PEG,P3HB M(n)的最大变化发生在0-1%PEG浓度范围内。用单甲氧基醚CH3O-PEG-OH-350和PEG-300补充孵育培养基会导致几乎相同的分子量降低。但是,四甘醇的二甲氧基醚不是降低分子量的有效试剂。因此,对于较低分子量的PEG,增强了PEG和PHA生产系统之间的相互作用,导致分子量降低,并且需要至少一个PEG链端官能团,该官能团可以是羟基。据信PEG以某种方式与嗜酸曲霉合成酶相互作用,以相对于链增长反应增加水的链终止速率。 [参考:38]

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