Durán Marcela, Silveira Camila P, Durán Nelson
Laboratory on Nanostructures Synthesis and Interactions with Biosystems (NanoBioss) Institute of Chemistry, Universidade Estadual de Campinas, Bloco I, Sala 239, Caixa Postal 6154, CEP 13081-970 Campinas, SP, Brazil.
IET Nanobiotechnol. 2015 Oct;9(5):314-23. doi: 10.1049/iet-nbt.2014.0054.
Although the formation mechanism of biogenically metallic nanoparticles is broadly associated to enzyme mediation, major attention has been given to the role of proteins and peptides in oxido-reduction of metallic ions leading to these nanostructures. Among the wide range of biomolecules that can act not only as capping agents but also as non-enzymatic agents to form nanoparticles, disulphide bridge-containing peptides and amino acids particularly stand out. The literature proposes that they actively participate in the process of nanoparticles' synthesis, with thiols groups and disulphide bridge moieties as the reaction catalytic sites. Similarly, denaturated enzymes containing exposed S-S or S-H moieties are also able to reduce metallic ions to form nanoparticles. This mini-review is focused on the biogenic synthesis of metallic nanoparticles such as gold, silver, copper, platinum, palladium, lead and selenium, in which proteins, peptides, reductases and even oxido-reductases act as non-enzymatic catalysts of the reduction reaction, opening economically and ecologically favourable perspectives in the nanoparticles synthesis field.
尽管生物源金属纳米颗粒的形成机制与酶介导广泛相关,但人们主要关注蛋白质和肽在金属离子氧化还原形成这些纳米结构过程中的作用。在众多不仅可作为封端剂而且可作为形成纳米颗粒的非酶试剂的生物分子中,含二硫键的肽和氨基酸尤为突出。文献表明它们积极参与纳米颗粒的合成过程,硫醇基团和二硫键部分作为反应催化位点。同样,含有暴露的S-S或S-H部分的变性酶也能够还原金属离子以形成纳米颗粒。本综述聚焦于金、银、铜、铂、钯、铅和硒等金属纳米颗粒的生物合成,其中蛋白质、肽、还原酶甚至氧化还原酶作为还原反应的非酶催化剂,为纳米颗粒合成领域开启了经济和生态上有利的前景。