| Literature DB >> 34572479 |
Nagaraj Basavegowda1, Kwang-Hyun Baek1.
Abstract
The development of food-borne and infectious diseases has increased globally at an anomalous rate and is combined with emerging social and economic problems. This highlights the need for new and improved antibacterial agents with novel and different mechanisms of action at regular intervals. Some chemical or artificial food additives are considered harmful if they are used beyond their permissible levels. Today, consumers are demanding alternative, green, safer, and natural food additives to increase the shelf life of food. Essential oils (EOs) are concentrated liquid mixtures of volatile compounds with antioxidant and antibacterial properties that can be used as natural, eco-friendly, renewable, and cost-effective additives. The use of combinations of different EOs and their components is a promising strategy to increase the synergistic and additive effects of EOs in foods. In this article, we review the recent literature on EOs concerning the chemical constituents, extraction methods, antioxidant and antibacterial activities, and their mechanisms of action. Additionally, we discuss the synergistic interaction of different EOs and their components, challenges, and future directions of EOs as natural food preservatives, with special emphasis on shelf life extension and applications in the packaging of food products.Entities:
Keywords: antibacterial; antioxidant; essential oils; food additives; food packaging; synergistic
Mesh:
Substances:
Year: 2021 PMID: 34572479 PMCID: PMC8466708 DOI: 10.3390/biom11091267
Source DB: PubMed Journal: Biomolecules ISSN: 2218-273X
Figure 1Chemical structural formulas of some major constituents of essential oils.
Major active chemical constituents of some important essential oils with molecular structure and plant sources.
| Essential Oil Constituents | Examples | Chemical Formula | Molecular Structure | Plant Source | Reference |
|---|---|---|---|---|---|
| Terpenes | C10H16 |
|
| [ | |
| Limonene | C10H16 |
|
| [ | |
| Sabinene | C10H16 |
|
| [ | |
| C10H14 |
|
| [ | ||
| Terpenoids | Linalool | C10H18O |
|
| [ |
| Thymol | C10H14O |
|
| [ | |
| Menthol | C10H20O |
|
| [ | |
| Carvacrol | C10H14O |
|
| [ | |
| Aldehydes | Cinnamaldehyde | C9H8O |
|
| [ |
| Phenols | Eugenol | C10H12O2 |
|
| [ |
| Chavicol | C9H10O |
|
| [ |
Extraction of essential oils from various sources using different methods.
| Essential Oils | Plant Source | Major Components | Extraction Methods | Ref. |
|---|---|---|---|---|
| Rosemary |
| Cineole, camphor, α-pinene | Hydrodistillation | [ |
| Neroli |
| Linalyl acetate, linalool, α-terpineol | Hydrodistillation | [ |
| Tobacco |
| β-Damascenone, β-damascone, cembrene | Solvent extraction | [ |
| Lemon |
| Limonene, γ-terpinene, β-pinene | Solvent extraction | [ |
| Chokeberry |
| Cyanidin-3-galactoside, quercetin-3-glucoside | Maceration | [ |
| Thyme |
| Rosmarinic acid, salvianolic acid | Maceration | [ |
| Lavender |
| Linalool, camphor, terpinen-4-ol | Supercritical fluid extraction | [ |
| Mint |
| Menthone, carvone, limonene | Supercritical fluid extraction | [ |
| Basil |
| Linalool, methyl-cinnamate, β-cubebene | Microwave-assisted extraction | [ |
| Epazote |
| Ascaridole, carvacrol, caryophyllene oxide | Microwave-assisted extraction | [ |
| Celery |
| Limonene, β-selinene, sedanenolid | Ultrasound-assisted extraction | [ |
| Sweet wormwood |
| Camphor, eucalyptol, myrtenol | Ultrasound-assisted extraction | [ |
Figure 2Proposed mechanism of hydrocarbon autoxidation and antioxidant properties of EOs. The typical three phases of free radical chain reactions, initiation, propagation, and termination are shown. RH represents a hydrocarbon, R∙ is an alkyl radical produced by the removal of a hydrogen atom from RH, ROO∙ is the peroxy radical formed by the reaction of R∙ with molecular oxygen; kp and kt are the propagation and termination rate constants, respectively, and kinh is the inhibition rate constant.
Figure 3Proposed mechanism of antibacterial action of essential oils.