Lycopene Production Research Articles

Amplifying Persistent Luminescence in Heavily Doped Nanopearls for Bioimaging and Solar-to-Chemical Synthesis.

Lanthanides are widely codoped in persistent luminescence phosphors (PLPs) to elevate defect concentration and enhance luminescence efficiency. However, the deleterious cross-relaxation between activators and lanthanides inevitably quenches persistent luminescence, particularly in heavily doped phosphors. Herein, we report a core-shell engineering strategy to minimize the unwanted cross-relaxation but retain the charge trapping capacity of heavily doped persistent luminescence phosphors by confining the activators and lanthanides in the core and shell, respectively. As a proof of concept, we prepared a series of codoped ZnGa2O4:Cr, Ln (CD-Ln, Ln = Nd, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb) and core-shell structured ZnGa2O4:Cr@ZnGa2O4:Ln (CS-Ln) nanoparticles. First-principles investigations suggested that lanthanide doping elevated the electron trap concentration for enhancing persistent luminescence, but energy transfer (ET) from Cr3+ to Ln3+ ions quenched the persistent luminescence. The spatial separation of Cr3+ and Ln3+ ions in the core-shell structured CS-Ln nanoparticles suppressed the ET from Cr3+ to Ln3+. Due to the efficient suppression of deleterious ET, the optimal doping concentration of Ln in CS-Ln was elevated 50 times compared to CD-Ln. Moreover, the persistent luminescence intensity of CS-5%Ln was up to 60 times that of the original ZnGa2O4:Cr. The CS-5%Ln displayed significantly improved signal-to-noise ratios in bioimaging. Further, the CS-Ln was interfaced with the lycopene-producing bacteria Rhodopseudomonas palustris for solar-to-chemical synthesis, and the lycopene productivity was increased by 190%. This work provides a reliable solution to fulfill the potential of lanthanides in enhancing persistent luminescence and can further promote the applications of persistent luminescence phosphors in biomedicine and solar-to-chemical synthesis.

Multi-enzyme assemblies both in the cell membrane and cytoplasm boost intracellular lycopene production.

The multi-enzyme assembly system demonstrates remarkable potential in enhancing both intracellular and extracellular enzyme catalysis. In this study, we employed a novel icosahedral protein cage, Mi3, as a protein scaffold and combined it with an ester bond-based peptide tagging system, ReverseTag/ReverseCatcher, to improve the enzymatic catalytic efficiency both in vitro and in vivo. In vitro, we fused ReverseTag to the N-terminal of exo-inulinase (EXINU) from Pseudomonas mucidolens, yielding ReverseTag-EXINU, which effectively bound to the surface of the ReverseCatcher-Mi3 protein cage. Following assembly, the Km value decreased from 16.3 to 7.9 g/L, while kcat/Km value increased from 1.9 to 3.0 L s-1 g-1, indicating a significant enhancement in substrate affinity and enzymatic catalytic efficiency. In vivo, we constructed a protein-cage multi-enzyme assembly system located in the cytoplasm and cell membrane based on ReverseTag/ReverseCatcher/Mi3 system. In lycopene biosynthesis, the production of lycopene after assembly was increased by 2.97 times compared to free enzyme catalysis. This strategy holds profound implications for fields such as synthetic biology and enzyme engineering.

Multi-gene precision editing tool using CRISPR-Cas12a/Cpf1 system in Ogataea polymorpha

BackgroundOgataea polymorpha, a non-conventional methylotrophic yeast, has demonstrated significant potential for heterologous protein expression and the production of high-value chemicals and biopharmaceuticals. However, the lack of precise and efficient genome editing tools severely hinders the construction of cell factories. Although the CARISP-Cas9 system has been established in Ogataea polymorpha, the gene editing efficiency, especially for multiple genes edition, needs to be further improved.ResultsIn this study, we developed an efficient CRISPR-Cpf1-mediated genome editing system in O. polymorpha that exhibited high editing efficiency for single gene (98.1 ± 1.7%), duplex genes (93.9 ± 2.4%), and triplex genes (94.0 ± 6.0%). Additionally, by knocking out non-homologous end joining (NHEJ) related genes, homologous recombination (HR) efficiency was increased from less than 30% to 90 ~ 100%, significantly enhancing precise genome editing capabilities. The increased HR rates enabled over 90% integration efficiency of triplex genes, as well as over 90% deletion rates of large DNA fragments up to 20 kb. Furthermore, using this developed CRISPR-Cpf1 system, triple genes were precisely integrated into the genome by one-step, enabling lycopene production in O. polymorpha.ConclusionsThis novel multiplexed genome-editing tool mediated by CRISPR-Cpf1 can realize the deletion and integration of multiple genes, which holds great promise for accelerating engineering efforts on this non-conventional methylotrophic yeast for metabolic engineering and genomic evolution towards its application as an industrial cell factory.

Developing an alternative medium for in-space biomanufacturing

In-space biomanufacturing provides a sustainable solution to facilitate long-term, self-sufficient human habitation in extraterrestrial environments. However, its dependence on Earth-supplied feedstocks renders in-space biomanufacturing economically nonviable. Here, we develop a process termed alternative feedstock-driven in-situ biomanufacturing (AF-ISM) to alleviate dependence on Earth-based resupply of feedstocks. Specifically, we investigate three alternative feedstocks (AF)—Martian and Lunar regolith, post-consumer polyethylene terephthalate, and fecal waste—to develop an alternative medium for lycopene production using Rhodococcus jostii PET strain S6 (RPET S6). Our results show that RPET S6 could directly utilize regolith simulant particles as mineral replacements, while the addition of anaerobically pretreated fecal waste synergistically supported its cell growth. Additionally, lycopene production using AF under microgravity conditions achieved levels comparable to those on Earth. Furthermore, an economic analysis shows significant lycopene production cost reductions using AF-ISM versus conventional methods. Overall, this work highlights the viability of AF-ISM for in-space biomanufacturing.

Screening and engineering of lycopene-producing strain Rhodococcus jostii for bio-upcycling of poly(ethylene terephthalate) waste.

Poly(ethylene terephthalate) (PET) is a widely used plastic, but its improper disposal has caused serious environmental pollution. The development of bioconversion for PET waste into high-value chemicals has gained significant attention as an innovative solution. In this study, a novel guided screening strategy involving mixed-bacteria fermentation and partitioned purification (MBF) was proposed to first successful isolate Rhodococcus jostii LETBE 8896, a strain capable of naturally producing 4μg/L of lycopene from PET hydrolysate. Transcriptomic analysis identified the methylerythritol 4-phosphate (MEP) pathway as key to lycopene biosynthesis, with IspG identified as a critical regulatory enzyme. R. jostii with ispG overexpression enhanced lycopene production, with 819μg/L in the simulated PET hydrolysate and 650μg/L in the PET hydrolysate. Additionally, the use of butylated hydroxytoluene (BHT) as an antioxidant significantly improved lycopene production at 1L scale level, achieving a maximum yield of 1865μg/L with a molar conversion rate of 50.36% from the PET hydrolysate, the highest reported for PET hydrolysate to date. These findings highlight the dual potential of R. jostii as a chassis strain for high-value chemical production and as a sustainable solution for PET upcycling. This study provides a novel approach to plastic waste management, contributing to the circular economy and global sustainability goals.

Engineering the Methylerythritol Phosphate Pathway and Using a Temporal Promoter for Enhanced Lycopene Production in Rhodobacter sphaeroides HY01.

Rhodobacter sphaeroides HY01 is a high-yield strain for industrial production of coenzyme Q10 (Q10), indicating its potential for producing other terpenoids. However, the production of Q10 substantially depletes isoprene precursors, nearly eliminating other terpenoids like spheroidene and spheroidenone commonly found in wild-type R. sphaeroides. Lycopene was used as an example to demonstrate its potential for terpenoid biosynthesis. By refactoring the methylerythritol phosphate (MEP) pathway, such as overexpressing crtE and introducing crtI4, lycopene production reached 126.1 mg/L in HY01. However, further overexpression of the deoxy-d-xylulose-5-phosphate synthase, 1-deoxy-d-xylulose 5-phosphate reductoisomerase, and isopentenyl-diphosphate isomerase genes led to strain degradation, significantly reducing lycopene production. Fine-tuning the engineered PrrAB two-component system, which upregulated the MEP pathway, increased lycopene production to 154.9 mg/L. Inspired by this result, a series of native promoters with varying strengths were identified and characterized through transcriptomic analysis during the late fermentation stage. Using these temporal promoters to control genes in the MEP pathway ultimately increased lycopene production to 283.1 mg/L, the highest reported in R. sphaeroides. These results underscore the potential of HY01 as a chassis for terpenoid biosynthesis.

Utilizing Microbial Electrochemical Methods to Enhance Lycopene Production in Rhodopseudomonas palustris.

Utilizing Rhodopseudomonas palustris (R. pal), this study constructed a dual-chamber microbial electrosynthesis system, based on microbial electrolysis cells, that was capable of producing lycopene. Cultivation within the electrosynthesis chamber yielded a lycopene concentration of 282.3722 mg/L when the optical density (OD) reached 0.6, which was four times greater than that produced by original strains. The mutant strain showed significantly higher levels of extracted riboflavin compared to the wild-type strain, and the riboflavin content of the mutant strain was 61.081 mg/L, which was more than 10 times that of the original strain. Furthermore, sequencing and analyses were performed on the mutant strains observed during the experiment. The results indicated differences in antibiotic resistance genes, carbohydrate metabolism-related genes, and the frequencies of functional genes between the mutant and original strains. The mutant strain displayed potential advantages in specific antibiotic resistance and carbohydrate degradation capabilities, likely attributable to its adaptation to electrogenic growth conditions. Moreover, the mutant strain demonstrated an enrichment of gene frequencies associated with transcriptional regulation, signal transduction, and amino acid metabolism, suggesting a complex genetic adaptation to electrogenic environments. This study presents a novel approach for the efficient and energy-conserving production of lycopene while also providing deeper insights into the genetic basis of electro-resistance genes.

Multiple metabolic engineering of Saccharomyces cerevisiae for the production of lycopene

AbstractLycopene is a high‐value‐added tetraterpenoid, which is widely used in cosmetics, medicine, food, and dietary supplements. The intracellular mevalonate pathway of Saccharomyces cerevisiae provides natural precursors for terpenoid product synthesis, so it is an excellent host for the heterologous production of lycopene. In this study, a recombinant strain named L10 with efficient lycopene production capability was constructed through multiple strategies, such as regulating the gene copy number of key enzymes, increasing nicotinamide adenine dinucleotide phosphate supply, and reducing squalene accumulation. Then, considering that intracellular lycopene accumulation can cause cytotoxicity to S. cerevisiae, we attempted to identify a transporter that can efficiently transport lycopene from intracellular to extracellular space. Molecular docking simulations predicted that the ATP‐binding cassette transporter Snq2p may be a potential transporter of lycopene, and its function in promoting lycopene secretion was further determined by overexpression verification. The lycopene secretion titer of the strain L10Z2 overexpressing Snq2p increased to 16.5 times that of the control at the shake‐flask level. After optimizing the galactose regulation system, the intracellular and secreted lycopene production of L11Z2 reached 2113.78 and 26.28 mg/L, respectively, after 150 h fed‐batch culture in a 3‐L bioreactor. This work provides a new research direction for efficient lycopene synthesis in S. cerevisiae cell factory.

Reconstitution of the Mevalonate Pathway for Improvement of Isoprenoid Production and Industrial Applicability in Escherichia coli.

Natural products, especially isoprenoids have many industrial applications, including medicine, fragrances, food additives, personal care and cosmetics, colorants, and even advanced biofuels. Recent advancements in metabolic engineering with synthetic biology and systems biology have drawn increased interest in microbial-based isoprenoid production. In order to engineer microorganisms to produce a large amount of value-added isoprenoids, great efforts have been made by employing various strategies from synthetic biology and systems biology. We also have engineered E. coli to produce various isoprenoids by targeting and engineering the isoprenoid biosynthetic pathways, methylerythritol phosphate (MEP), and mevalonate (MVA) pathways. Here, we introduced new combinations of the MVA pathway in E. coli with genes from biosafety level 1 (BSL 1) organisms. The reconstituted MVA pathway constructs (pSCS) are not only preferred to the living modified organism (LMO) regulation, but they also improved carotenoid production. In addition, the pSCS constructs resulted in enhanced lycopene production and cell-specific productivity compared to the previous MVA pathway combination (pSNA) in fed-batch fermentation. The pSCS constructs would not only bring an increase in isoprenoid production in E. coli, but they could be an efficient system to be applied for the industrial production of isoprenoids with industry-preferred genetic combinations.

Techno-Economic Analysis of Lycopene Production from Tomato Waste Using the Pervaporation Process

Techno-Economic Analysis of Lycopene Production from Tomato Waste Using the Pervaporation Process

Recent advances in lycopene and germacrene a biosynthesis and their role as antineoplastic drugs.

Sesquiterpenes and tetraterpenes are classes of plant-derived natural products with antineoplastic effects. While plant extraction of the sesquiterpene, germacrene A, and the tetraterpene, lycopene suffers supply chain deficits and poor yields, chemical synthesis has difficulties in separating stereoisomers. This review highlights cutting-edge developments in producing germacrene A and lycopene from microbial cell factories. We then summarize the antineoplastic properties of β-elemene (a thermal product from germacrene A), sesquiterpene lactones (metabolic products from germacrene A), and lycopene. We also elaborate on strategies to optimize microbial-based germacrene A and lycopene production.

Optimizing multicopy chromosomal integration for stable high-performing strains.

The copy number of genes in chromosomes can be modified by chromosomal integration to construct efficient microbial cell factories but the resulting genetic systems are prone to failure or instability from triggering homologous recombination in repetitive DNA sequences. Finding the optimal copy number of each gene in a pathway is also time and labor intensive. To overcome these challenges, we applied a multiple nonrepetitive coding sequence calculator that generates sets of coding DNA sequence (CDS) variants. A machine learning method was developed to calculate the optimal copy number combination of genes in a pathway. We obtained an engineered Yarrowia lipolytica strain for eicosapentaenoic acid biosynthesis in 6 months, producing the highest titer of 27.5 g l-1 in a 50-liter bioreactor. Moreover, the lycopene production in Escherichia coli was also greatly improved. Importantly, all engineered strains of Y. lipolytica, E. coli and Saccharomyces cerevisiae constructed with nonrepetitive CDSs maintained genetic stability.

Biokinetics modelling of lycopene-producing E. coli fermentation using PAT methodology

Process analytical technology (PAT), which espouses the use of in-line analytics to monitor critical process parameters (CPPs), critical quality attributes (CQAs) and mathematical analyses, was employed to elucidate underlying carbon-source metabolism of a lycopene-producing E. coli strain during non-induced and induced batch fermentations. In-line dielectric and Raman spectroscopies were deployed to monitor real-time culture biomass viability (X), primary substrate glucose (S), and intracellular lycopene production (P), together with off-line HPLC quantification of broth acetate (A). In-line PAT monitoring enabled identification of two distinct metabolic regimes during induced batch run with lycopene accumulation. Biokinetics mathematical models using differential-algebraic equations and Monod-type conversions were formulated to explain experimentally measured dynamic trends of the state variables X, S, A and P during the batch runs. Their optimized model parameters and seven dimensionless ratios reflected changes in concentrations or rates relative to glucose, acetate, or lycopene. The calculated rates of culture growth, glucose utilization, acetate accumulation, and lycopene production revealed salient underlying carbon metabolic shifts and transient trends that explained phenomenological observations: such as growth patterns, carbon source usage, overflow mechanism, cellular affinity or inhibitory effects, and lycopene cytotoxicity. These parameters and dimensionless ratios could be used to compare novel strains, develop in silico simulations for scale-up or troubleshoot batch-to-batch variations.

Tomato genotype but not crop water deficit matters for tomato health benefits in diet-induced obesity of C57BL/6JRj male mice

Several studies have linked the intake of lycopene and/or tomato products with improved metabolic health under obesogenic regime. The aim was to evaluate the differential impact of supplementations with several tomato genotypes differing in carotenoid content and subjected to different irrigation levels on obesity-associated disorders in mice. In this study, 80 male C57BL/6JRj mice were assigned into 8 groups to receive: control diet, high fat diet, high fat diet supplemented at 5 % w/w with 4 tomato powders originating from different tomato genotypes cultivated under control irrigation: H1311, M82, IL6-2, IL12-4. Among the 4 genotypes, 2 were also cultivated under deficit irrigation, reducing the irrigation water supply by 50 % from anthesis to fruit harvest. In controlled irrigation treatment, all genotypes significantly improved fasting glycemia and three of them significantly lowered liver lipids content after 12 weeks of supplementation. In addition, IL6-2 genotype, rich in β-carotene, significantly limited animal adiposity, body weight gain and improved glucose homeostasis as highlighted in glucose and insulin tolerance tests. No consistent beneficial or detrimental impact of deficit irrigation to tomato promoting health benefits was found. These findings imply that the choice of tomato genotype can significantly alter the composition of fruit carotenoids and phytochemicals, thereby influencing the anti-obesogenic effects of the fruit. In contrast, deficit irrigation appears to have an overall insignificant impact on enhancing the health benefits of tomato powder in this context, particularly when compared to the genotype-related variations in carotenoid content.

Expanding the CRISPR Toolbox for Engineering Lycopene Biosynthesis in Corynebacterium glutamicum.

Lycopene represents one of the central compounds in the carotenoid pathway and it exhibits a potent antioxidant ability with wide potential applications in medicine, food, and cosmetics. The microbial production of lycopene has received increasing concern in recent years. Corynebacterium glutamicum (C. glutamicum) is considered to be a safe and beneficial industrial production platform, naturally endowed with the ability to produce lycopene. However, the scarcity of efficient genetic tools and the challenge of identifying crucial metabolic genes impede further research on C. glutamicum for achieving high-yield lycopene production. To address these challenges, a novel genetic editing toolkit, CRISPR/MAD7 system, was established and developed. By optimizing the promoter, ORI and PAM sequences, the CRISPR/MAD7 system facilitated highly efficient gene deletion and exhibited a broad spectrum of PAM sites. Notably, 25 kb of DNA from the genome was successfully deleted. In addition, the CRISPR/MAD7 system was effectively utilized in the metabolic engineering of C. glutamicum, allowing for the simultaneous knockout of crtEb and crtR genes in one step to enhance the accumulation of lycopene by blocking the branching pathway. Through screening crucial genes such as crtE, crtB, crtI, idsA, idi, and cg0722, an optimal carotenogenic gene combination was obtained. Particularly, cg0722, a membrane protein gene, was found to play a vital role in lycopene production. Therefore, the CBIEbR strain was obtained by overexpressing cg0722, crtB, and crtI while strategically blocking the by-products of the lycopene pathway. As a result, the final engineered strain produced lycopene at 405.02 mg/L (9.52 mg/g dry cell weight, DCW) in fed-batch fermentation, representing the highest reported lycopene yield in C. glutamicum to date. In this study, a powerful and precise genetic tool was used to engineer C. glutamicum for lycopene production. Through the modifications between the host cell and the carotenogenic pathway, the lycopene yield was stepwise improved by 102-fold as compared to the starting strain. This study highlights the usefulness of the CRISPR/MAD7 toolbox, demonstrating its practical applications in the metabolic engineering of industrially robust C. glutamicum.

Characteristics of the existing methods for obtaining carotenes from carotenoid concentrates

Carotenes, which simultaneously have the properties of natural dyes and biologically active substances that have a positive effect on human health and life expectancy, are becoming increasingly widespread in the food, pharmacological and cosmetic industries. This necessitates an increase in the production of carotenes on an industrial scale. For use in food technologies, an encapsulated form of carotenes is recommended, which requires their high purity. The purpose of this study is to analyze domestic and foreign scientific, technical and patent information on existing methods for obtaining carotenes from carotenoid concentrates to determine the direction of research for the development of technology for the production of carotenes, in particular lycopene, ensuring the production of high purity lycopene from carotenoid concentrates, as well as increasing release of lycopene. The issues of using chromatographic methods for isolating lycopene, their advantages and disadvantages, as well as the use of non-polar and low-polar organic solvents for isolating lycopene from carotenoid concentrate are considered. The promising direction of research on the use of adsorption resins in the isolation of lycopene from carotenoid concentrates is noted.It has been concluded that the currently existing methods for obtaining carotenes from carotenoid concentrates, in particular lycopene, are quite technically complex and time-consuming. Some of the mallow the production of high purity lycopene, but the yield of lycopene is so low that their industrial scaling seems impractical. Taking this into account, research is being updated in the field of developing a technology for producing lycopene from a carotenoid concentrate, providing a high yield of high purity lycopene, with the possibility of its implementation on an industrial scale.

Application of ionic liquid ultrasound-assisted extraction (IL-UAE) of lycopene from guava (Psidium guajava L.) by response surface methodology and artificial neural network-genetic algorithm

Lycopene-rich guava (Psidium guajava L.) exhibits significant economic potential as a functional food ingredient, making it highly valuable for the pharmaceutical and agro-food industries. However, there is a need to enhance the extraction methods of lycopene to fully exploit its beneficial uses. In this study, we evaluated various ionic liquids to identify the most effective one for extracting lycopene from guava. Among thirteen ionic liquids with varying carbon chains or anions, 1-butyl-3-methylimidazolium chloride demonstrated the highest productivity. Subsequently, a single-factor experiment was employed to test the impact of several parameters on the efficiency of lycopene extraction using this selected ionic liquid. These parameters included extraction time, ultrasonic power, liquid-solid ratio, concentration of the ionic liquid, as well as material particle size. Moreover, models of artificial neural networks using genetic algorithms (ANN-GA) and response surface methodology (RSM) were employed to comprehensively assess the first four key parameters. The optimized conditions for ionic liquid ultrasound-assisted extraction (IL-UAE) were determined as follows: 33 min of extraction time, 225 W of ultrasonic power, 22 mL/g of liquid-solid ratio, 3.0 mol/L of IL concentration, and extraction cycles of three. Under these conditions, lycopene production reached an impressive yield of 9.35 ± 0.36 mg/g while offering advantages such as high efficiency, time savings, preservation benefits, and most importantly environmental friendliness.

Enhancement of Lycopene Synthesis via Low-Frequency Alternating Magnetic Field in Brassica trispora

In recent years, magnetic fields have emerged as a non-thermophysical treatment with a significant impact on microbial fermentation processes. Brassica trispora is a microorganism known for its industrial-scale production of lycopene and high yield of single cells. This study aimed to investigate the impact of low-frequency magnetic fields on lycopene synthesis by Brassica trispora and elucidate the underlying mechanism for enhancing lycopene yield. The results indicate that both the intensity and duration of the magnetic field treatment influenced the cells. Exposing the cells to a 0.5 mT magnetic field for 48 h on the second day of fermentation resulted in a lycopene yield of 25.36 mg/g, representing a remarkable increase of 244.6% compared to the control group. Transcriptome analysis revealed that the alternating magnetic field significantly upregulated genes related to ROS and the cell membrane structure, leading to a substantial increase in lycopene production. Scanning electron microscopy revealed that the magnetic field treatment resulted in a rough, loose, and wrinkled surface morphology of the mycelium, along with a few micropores, thereby altering the cell membrane permeability to some extent. Moreover, there was a significant increase in intracellular ROS content, cell membrane permeability, key enzyme activity involved in lycopene metabolism, and ROS-related enzyme activity. In conclusion, the alternating frequency magnetic field can activate a self-protective mechanism that enhances lycopene synthesis by modulating intracellular ROS content and the cell membrane structure. These findings not only deepen our understanding of the impact of magnetic fields on microbial growth and metabolism but also provide valuable insights for developing innovative approaches to enhance carotenoid fermentation.

Studying the composition of a tomato supernatant

One of the ways to improve people's health through food is the industrial production of products, the so-called "health" group, which currently includes soft drinks, including special-purpose ones. Drinks are the most technologically advanced basis for creating new types of functional products. Soft drinks are widely used in therapeutic and preventive nutrition. They are useful not only for the normalization of water-electrolyte metabolism, but also for optimizing the chemical structure of the diet. One of the promising functional components of beverages obtained during the production of lycopene from tomatoes is a supernatant. There is no information about its component composition in the available literature. A qualitative and quantitative study of the supernatants of tomatoes of different varieties is given. Some carbohydrates, water-soluble vitamins, micro- and macronutrients, organic acids, and flavonoids have been identified. The identified nutrients that are part of the tomato supernatants allow them to be used in soft drinks, including for special purposes. The study of the content of micro- and macronutrients did not reveal significant differences in the supernatant obtained from different varieties of tomatoes, but it is worth noting a fairly high content of iron and copper. It was found that the largest amount of vitamin C was found in a supernatant obtained from tomatoes of the Volgogradsky variety. Despite the fact that the supernatant is a by-product of carotenoid production, it has a range of nutrients that are certainly valuable to humans and can be used in food technology, in particular soft drinks, including special-purpose ones. The next stage of the work will be the development of a technology for preparing a special-purpose drink using supernatants obtained from different varieties of tomatoes. The research was carried out at the expense of a grant from the Russian Science Foundation № 23-26-00217, https://rscf.ru/project/23-26-00217/

Multi-modular metabolic engineering and efflux engineering for enhanced lycopene production in recombinant Saccharomyces cerevisiae.

In this research, lycopene production in yeast was markedly enhanced by integrating a multi-modular approach, acetate signaling-based down-regulation of competitive pathways, and an efflux optimization strategy.