Chowdhuri Sampreeti, Cole Christian M, Devaraj Neal K
Department of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Drive, Building, Urey Hall 4120, La Jolla, CA, 92093, USA.
Chembiochem. 2016 May 17;17(10):886-9. doi: 10.1002/cbic.201500643. Epub 2016 Mar 29.
Liposomes form spontaneously by the assimilation of phospholipids, the primary component of cell membranes. Due to their unique ability to form selectively permeable bilayers in situ, they are widely used as nanocarriers for drug and small-molecule delivery. However, there is a lack of straightforward methodologies to encapsulate living microorganisms. Here we demonstrate the successful encapsulation of whole cells in phospholipid vesicles by using the inverse-emulsion technique of generating unilamellar vesicles. This method of liposome preparation allows for a facile encapsulation of large biomaterials that previously was not easily attainable. Using Escherichia coli as a model organism, we found that liposomes can protect the bacterium against external protease degradation and from harsh biological environments. Liposomes prepared by the inverse-emulsion method were also capable of encapsulating yeast and were found to be naturally susceptible to hydrolysis by enzymes such as phospholipases, thus highlighting their potential role as cell delivery carriers.
脂质体通过细胞膜的主要成分磷脂的同化作用自发形成。由于它们具有在原位形成选择性渗透双层的独特能力,因此被广泛用作药物和小分子递送的纳米载体。然而,缺乏直接的方法来封装活的微生物。在这里,我们展示了通过使用生成单层囊泡的反相乳液技术成功地将全细胞封装在磷脂囊泡中。这种脂质体制备方法允许轻松封装以前不容易获得的大型生物材料。以大肠杆菌作为模式生物,我们发现脂质体可以保护细菌免受外部蛋白酶降解以及恶劣生物环境的影响。通过反相乳液法制备的脂质体也能够封装酵母,并且发现它们天然易受磷脂酶等酶的水解作用,从而突出了它们作为细胞递送载体的潜在作用。