» Articles » PMID: 36752618

Systematic Adaptation of Bacillus Licheniformis to 2-Phenylethanol Stress

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

The compound 2-phenylethanol (2-PE) is a bulk flavor and fragrance with a rose-like aroma that can be produced by microbial cell factories, but its cellular toxicity inhibits cellular growth and limits strain performance. Specifically, the microbe Bacillus licheniformis has shown a strong tolerance to 2-PE. Understanding these tolerance mechanisms is crucial for achieving the hyperproduction of 2-PE. In this report, the mechanisms of B. licheniformis DW2 resistance to 2-PE were studied by multi-omics technology coupled with physiological and molecular biological approaches. 2-PE induced reactive oxygen species formation and affected nucleic acid, ribosome, and cell wall synthesis. To manage 2-PE stress, the antioxidant and global stress response systems were activated; the repair system of proteins and homeostasis of the ion and osmotic were initiated. Furthermore, the tricarboxylic acid cycle and NADPH synthesis pathways were upregulated; correspondingly, scanning electron microscopy revealed that cell morphology was changed. These results provide deeper insights into the adaptive mechanisms of B. licheniformis to 2-PE and highlight the potential targets for genetic manipulation to enhance 2-PE resistance. The ability to tolerate organic solvents is essential for bacteria producing these chemicals with high titer, yield, and productivity. As exemplified by 2-PE, bioproduction of 2-PE represents a promising alternative to chemical synthesis and plant extraction approaches, but its toxicity hinders successful large-scale microbial production. Here, a multi-omics approach is employed to systematically study the mechanisms of B. licheniformis DW2 resistance to 2-PE. As a 2-PE-tolerant strain, B. licheniformis displays multifactorial mechanisms of 2-PE tolerance, including activating global stress response and repair systems, increasing NADPH supply, changing cell morphology and membrane composition, and remodeling metabolic pathways. The current work yields novel insights into the mechanisms of B. licheniformis resistance to 2-PE. This knowledge can also be used as a clue for improving bacterial performances to achieve industrial-scale production of 2-PE and potentially applied to the production of other relevant organic solvents, such as tyrosol and hydroxytyrosol.

Citing Articles

Overexpressing Endopeptidase Inhibitor IseA Enhances Biomass and Biochemical Production of Bacillus licheniformis.

Zhang Y, He P, Hu S, Zhang R, Asfandyar , Chen S Curr Microbiol. 2025; 82(3):116.

PMID: 39903300 DOI: 10.1007/s00284-025-04096-2.


Heterologous and High Production of Ergothioneine in by Using Genes from Anaerobic Bacteria.

Liu Z, Xiao F, Zhang Y, Lu J, Li Y, Shi G Metabolites. 2025; 15(1).

PMID: 39852388 PMC: 11767532. DOI: 10.3390/metabo15010045.


Biotechnological 2-Phenylethanol Production: Recent Developments.

Bernardino A, Torres C, Crespo J, Reis M Molecules. 2024; 29(23).

PMID: 39683919 PMC: 11644012. DOI: 10.3390/molecules29235761.


Metabolic and tolerance engineering of Komagataella phaffii for 2-phenylethanol production through genome-wide scanning.

Sun L, Gao Y, Sun R, Liu L, Lin L, Zhang C Biotechnol Biofuels Bioprod. 2024; 17(1):107.

PMID: 39039584 PMC: 11265028. DOI: 10.1186/s13068-024-02536-y.


Analysis of heterologous expression of phaCBA promotes the acetoin stress response mechanism in Bacillus subtilis using transcriptomics and metabolomics approaches.

Li T, Li H, Zhong L, Qin Y, Guo G, Liu Z Microb Cell Fact. 2024; 23(1):58.

PMID: 38383407 PMC: 10880289. DOI: 10.1186/s12934-024-02334-z.

References
1.
Wang Y, Zhang H, Lu X, Zong H, Zhuge B . Advances in 2-phenylethanol production from engineered microorganisms. Biotechnol Adv. 2019; 37(3):403-409. DOI: 10.1016/j.biotechadv.2019.02.005. View

2.
Liu J, Bai Y, Fan T, Zheng X, Cai Y . Unveiling the Multipath Biosynthesis Mechanism of 2-Phenylethanol in . J Agric Food Chem. 2020; 68(29):7684-7690. DOI: 10.1021/acs.jafc.0c02918. View

3.
Jiang J, Zhu S, Zhang Y, Sun X, Hu X, Huang H . Integration of lipidomic and transcriptomic profiles reveals novel genes and regulatory mechanisms of Schizochytrium sp. in response to salt stress. Bioresour Technol. 2019; 294:122231. DOI: 10.1016/j.biortech.2019.122231. View

4.
Gonzalez L, Garcia-Huertas P, Triana-Chavez O, Garcia G, Murta S, Mejia-Jaramillo A . Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi. Mol Microbiol. 2017; 106(5):704-718. DOI: 10.1111/mmi.13830. View

5.
Liu P, Cheng Y, Yang M, Liu Y, Chen K, Long C . Mechanisms of action for 2-phenylethanol isolated from Kloeckera apiculata in control of Penicillium molds of citrus fruits. BMC Microbiol. 2014; 14:242. PMC: 4177429. DOI: 10.1186/s12866-014-0242-2. View