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玉米醇溶蛋白单层膜:表征及其与(生物)表面活性剂的相互作用

Zein Monolayers: Characterization and Interaction with (Bio)surfactants.

作者信息

Wojciechowski Kamil, Campana Mario, Samel Agnieszka, Baran Emilia

机构信息

Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, Warsaw 00-664, Poland.

Department of Chemistry, University of Warmia and Mazury in Olsztyn, Pl. Łódzki 4, Olsztyn 10-721, Poland.

出版信息

Langmuir. 2025 Aug 5;41(30):20174-20183. doi: 10.1021/acs.langmuir.5c02426. Epub 2025 Jul 23.

DOI:10.1021/acs.langmuir.5c02426
PMID:40696943
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12333351/
Abstract

Zein is the main protein of corn seeds, which is often employed in food packaging and as a model of keratin. In this study, zein monolayers were deposited from nonconventional solvents: aqueous ethanol and acetic acid, on pure water that was later exchanged for 1% (bio)surfactant solutions: SDS, CTAB, Triton X-100, and the saponin-rich plant extracts of soapwort ( L.) and cowherb ( [P. Mill.] Rauschert), as well as Quillaja bark saponins (QBS). The monolayers on pure water could be reversibly compressed up to ∼47 mN/m. On the basis of neutron reflectivity (NR) results, the liquid expanded-liquid expanded (LE-LE) transition observed at π ≈ 30 mN/m was assigned to an expulsion of the well-packed monolayer initially located on the air side of the interface, toward the aqueous side. The phase transition was accompanied by an increase in the layer thickness (from ∼1 to ∼6 nm) and the adsorbed amount (from ∼1.7 to ∼5.0 mg/m). In contrast to the saponin-rich solutions, the synthetic surfactants introduced to the subphase easily removed the zein monolayer precompressed to π = 30 mN/m, although the mechanism was different for the ionic (continuous displacement) and for the nonionic (orogenic-like). The zein layers at Si/water and their resistance to the detergent activity of SDS and QBS were assessed using NR, proving that the layers cast from acetic acid showed slightly higher mechanical strength than those cast from aqueous ethanol.

摘要

玉米醇溶蛋白是玉米种子的主要蛋白质,常用于食品包装并作为角蛋白的模型。在本研究中,玉米醇溶蛋白单分子层由非常规溶剂(乙醇水溶液和乙酸)沉积在纯水上,随后将纯水换成1%(生物)表面活性剂溶液:十二烷基硫酸钠(SDS)、十六烷基三甲基溴化铵(CTAB)、聚山梨醇酯80(Triton X - 100),以及富含皂苷的肥皂草(L.)和麦仙翁([P. Mill.] Rauschert)植物提取物,还有皂树树皮皂苷(QBS)。纯水上的单分子层可可逆压缩至约47 mN/m。基于中子反射率(NR)结果,在π≈30 mN/m处观察到的液-液扩张(LE - LE)转变被归因于最初位于界面空气侧的紧密堆积单分子层向水相侧的排出。相变伴随着层厚度的增加(从约1到约6 nm)和吸附量的增加(从约1.7到约5.0 mg/m)。与富含皂苷的溶液不同,引入亚相的合成表面活性剂很容易去除预压缩至π = 30 mN/m的玉米醇溶蛋白单分子层,尽管离子型(连续置换)和非离子型(类造山作用)的机制不同。使用NR评估了硅/水处的玉米醇溶蛋白层及其对SDS和QBS去污活性的抗性,证明从乙酸中浇铸的层比从乙醇水溶液中浇铸的层具有略高的机械强度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/07a2556d26a7/la5c02426_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/a645541ce921/la5c02426_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/84c98417938d/la5c02426_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/e1ee2e89331a/la5c02426_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/66924078bb87/la5c02426_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/07a2556d26a7/la5c02426_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/a645541ce921/la5c02426_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/84c98417938d/la5c02426_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/e1ee2e89331a/la5c02426_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/66924078bb87/la5c02426_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a91b/12333351/07a2556d26a7/la5c02426_0005.jpg

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