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由壳聚糖、水醇提取物和酵母组成的合成-生物活性材料的合成与设计及其作为生物催化剂的应用

Synthesis and Design of a Synthetic-Living Material Composed of Chitosan, Hydroalcoholic Extract, and Yeast with Applications as a Biocatalyst.

作者信息

Caamal-Herrera Isabel O, Erreguin-Isaguirre Mariana B, León-Buitimea Angel, Morones-Ramírez José R

机构信息

School of Chemistry, Autonomous University of Nuevo Leon (UANL), San Nicolas de los Garza, Nuevo Leon 66455, Mexico.

Applied Microbiology Department, NanoBiotechnology Research Group, Research Center on Biotechnology and Nanotechnology, School of Chemical Sciences, Autonomous University of Nuevo Leon, PIIT, Km 10 Autopista al Aeropuerto Mariano Escobedo, Apodaca, Nuevo Leon 66629, Mexico.

出版信息

ACS Omega. 2023 Apr 1;8(14):12716-12729. doi: 10.1021/acsomega.2c07847. eCollection 2023 Apr 11.

DOI:10.1021/acsomega.2c07847
PMID:37065078
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10099135/
Abstract

Design and development of materials that couple synthetic and living components allow taking advantage of the complexity of biological systems within a controlled environment. However, their design and fabrication represent a challenge for material scientists since it is necessary to synthesize synthetic materials with highly specialized biocompatible and physicochemical properties. The design of synthetic-living materials (vita materials) requires materials capable of hosting cell ingrowth and maintaining cell viability for extended periods. Vita materials offer various advantages, from simplifying product purification steps to controlling cell metabolic activity and improving the resistance of biological systems to external stress factors, translating into reducing bioprocess costs and diversifying their industrial applications. Here, chitosan sponges, functionalized with hydroalcoholic extract, were synthesized using the freeze-drying method; they showed small pore sizes (7.58 μm), high porosity (97.95%), high water absorption (1695%), and thermal stability, which allows the material to withstand sterilization conditions. The sponges allowed integration of 58.34% of viable cells, and the cell viability was conserved 12 h post-process (57.14%) under storage conditions [refrigerating temperature (4 °C) and without a nutrient supply]. In addition, the synthesized vita materials conserved their biocatalytic activity after 7 days of the integration process, which was evaluated through glucose consumption and ethanol production. The results in this paper describe the synthesis of complex vita materials and demonstrate that biochemically modified chitosan sponges can be used as a platform material to host living and metabolically active yeast with diverse applications as biocatalysts.

摘要

将合成成分与活性成分相结合的材料的设计与开发,能够在可控环境中利用生物系统的复杂性。然而,其设计和制造对材料科学家而言是一项挑战,因为有必要合成具有高度专业化生物相容性和物理化学性质的合成材料。合成-活性材料(活性材料)的设计需要能够支持细胞向内生长并长时间维持细胞活力的材料。活性材料具有多种优势,从简化产品纯化步骤到控制细胞代谢活性,以及提高生物系统对外界应激因素的抵抗力,这意味着可以降低生物工艺成本并使其工业应用多样化。在此,使用冷冻干燥法合成了用含酒精提取物功能化的壳聚糖海绵;它们显示出小孔径(7.58μm)、高孔隙率(97.95%)、高吸水性(1695%)和热稳定性,这使得该材料能够承受灭菌条件。这些海绵能够整合58.34%的活细胞,并且在储存条件下(冷藏温度4°C且无营养供应)处理后12小时细胞活力得以保持(57.14%)。此外,合成的活性材料在整合过程7天后仍保留其生物催化活性,这通过葡萄糖消耗和乙醇产生进行评估。本文的结果描述了复杂活性材料的合成,并证明经生物化学修饰的壳聚糖海绵可作为一种平台材料,用于容纳具有多种生物催化剂应用的活的且具有代谢活性的酵母。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/0c0496c43622/ao2c07847_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/998063c566db/ao2c07847_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/f624d26d0988/ao2c07847_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/a2e26b9edeee/ao2c07847_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/0db7a6e0c01e/ao2c07847_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/79ae0e9ed3db/ao2c07847_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/ca87863ea10a/ao2c07847_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/c4eb099c5129/ao2c07847_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/e085ba0478fd/ao2c07847_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/0c0496c43622/ao2c07847_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/998063c566db/ao2c07847_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/f624d26d0988/ao2c07847_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/a2e26b9edeee/ao2c07847_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/0db7a6e0c01e/ao2c07847_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/79ae0e9ed3db/ao2c07847_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/ca87863ea10a/ao2c07847_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/c4eb099c5129/ao2c07847_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/e085ba0478fd/ao2c07847_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9c/10099135/0c0496c43622/ao2c07847_0010.jpg

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