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双二氢阿魏酰基-1,4-丁二醇含量对聚(3-羟基丁酸酯)化学、酶促和真菌降解过程的影响

Impact of Bis--dihydroferuloyl-1,4-butanediol Content on the Chemical, Enzymatic and Fungal Degradation Processes of Poly(3-hydroxybutyrate).

作者信息

Carboué Quentin, Fadlallah Sami, Werghi Yasmine, Longé Lionel, Gallos Antoine, Allais Florent, Lopez Michel

机构信息

URD Agro-Biotechnologies Industrielles (ABI), CEBB, AgroParisTech, 3 Rue des Rouges-Terres, 51110 Pomacle, France.

出版信息

Polymers (Basel). 2022 Apr 11;14(8):1564. doi: 10.3390/polym14081564.

Abstract

Poly-β-hydroxybutyrate (PHB) is a very common bio-based and biocompatible polymer obtained from the fermentation of soil bacteria. Due to its important crystallinity, PHB is extremely brittle in nature, which results in poor mechanical properties with low extension at the break. To overcome these issues, the crystallinity of PHB can be reduced by blending with plasticizers such as ferulic acid derivatives, e.g., bis--dihydroferuloyl-1,4-butanediol (BDF). The degradation potential of polymer blends of PHB containing various percentages (0, 5, 10, 20, and 40 w%) of BDF was investigated through chemical, enzymatic and fungal pathways. Chemical degradation revealed that, in 0.25 M NaOH solution, the presence of BDF in the blend was necessary to carry out the degradation, which increased as the BDF percentage increased. Whereas no enzymatic degradation could be achieved in the tested conditions. Fungal degradation was achieved with a strain isolated from the soil and monitored through imagery processing. Similar to the chemical degradation, higher BDF content resulted in higher degradation by the fungus.

摘要

聚-β-羟基丁酸酯(PHB)是一种非常常见的生物基且具有生物相容性的聚合物,它由土壤细菌发酵制得。由于其重要的结晶性,PHB在本质上极其脆,这导致其机械性能较差,断裂伸长率较低。为克服这些问题,可通过与增塑剂(如阿魏酸衍生物,例如双-二氢阿魏酰基-1,4-丁二醇(BDF))共混来降低PHB的结晶性。通过化学、酶促和真菌途径研究了含有不同百分比(0、5、10、20和40重量%)BDF的PHB聚合物共混物的降解潜力。化学降解表明,在0.25 M氢氧化钠溶液中,共混物中BDF的存在是进行降解所必需的,且随着BDF百分比的增加而增加。而在测试条件下无法实现酶促降解。用从土壤中分离出的菌株实现了真菌降解,并通过图像处理进行监测。与化学降解类似,较高含量的BDF导致真菌降解程度更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c291/9031392/9bf9f9185b9d/polymers-14-01564-g001.jpg

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