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Flexible gas sensors capable of working at room temperature are in great demand for the Internet-of-things (IoT) revolution. Although molybdenum disulfide (MoS2) is a promising material for NO2 gas sensing, the influence of morphology on sensing performance is not well understood. Existing gas sensors using conventional electrodes involve complex fabrication processes, resulting in high cost, thus severely limiting their ubiquitous application. In this paper, the design, fabrication, and characterization of MoS2 gas sensors utilizing laser-induced graphene (LIG) electrodes are presented. Morphology evolution of MoS2 nanostructures and the resulting gas sensing performance trade-offs are discussed. The flexibility and mechanical robustness of the sensors utilizing LIG electrodes have also been confirmed to be excellent. Overall, high performance in gas sensing combined with low susceptibility to mechanical damage enables the sensor to serve a variety of wearable sensory applications. [ABSTRACT FROM AUTHOR]

Flavonoids, a significant group of natural polyphenolic compounds, possess a broad spectrum of pharmacological effects. Recent advances in the systematic metabolic engineering of yeast cell factories (YCFs) provide new opportunities for enhanced flavonoid production. Herein, we outline the latest research progress on typical flavonoid products in YCFs. Advanced engineering strategies involved in flavonoid biosynthesis are discussed in detail, including enhancing precursor supply, cofactor engineering, optimizing core pathways, eliminating competitive pathways, relieving transport limitations, and dynamic regulation. Additionally, we highlight the existing problems in the biosynthesis of flavonoid glucosides in yeast, such as endogenous degradation of flavonoid glycosides, substrate promiscuity of UDP-glycosyltransferases, and an insufficient supply of UDP-sugars, with summaries on the corresponding solutions. Discussions also cover other typical postmodifications like prenylation and methylation, and the recent biosynthesis of complex flavonoid compounds in yeast. Finally, a series of advanced technologies are envisioned, i.e., semirational enzyme engineering, ML/DL algorithn, and systems biology, with the aspiration of achieving large-scale industrial production of flavonoid compounds in the future.

Liquid fermentation is the primary method for GA 3 production using Fusarium fujikuroi . However, production capacity is limited due to unknown metabolic pathways. To address this, we constructed a genome-scale metabolic model ( i CY1235) with 1753 reactions, 1979 metabolites, and 1235 genes to understand the GA 3 regulation mechanisms. The model was validated by analyzing growth rates under different glucose uptake rates and identifying essential genes. We used the model to optimize fermentation conditions, including carbon sources and dissolved oxygen. Through the OptForce algorithm, we identified 20 reactions as targets. Overexpressing FFUJ_02053 and FFUJ_14337 resulted in a 37.5 and 75% increase in GA3 titers, respectively. These targets enhance carbon flux toward GA 3 production. Our model holds promise for guiding the metabolic engineering of F. fujikuroi to achieve targeted overproduction. In summary, our study utilizes the i CY1235 model to understand GA 3 regulation, optimize fermentation conditions, and identify specific targets for enhancing GA 3 production through metabolic engineering.

Patchoulol is an important sesquiterpene alcohol with a strong and lasting odor, which has led to prominent applications in perfumes and cosmetics. In this study, systematic metabolic engineering strategies were adopted to create an efficient yeast cell factory for patchoulol overproduction. First, a baseline strain was constructed by selecting a highly active patchoulol synthase. Subsequently, the mevalonate precursor pool was expanded to boost patchoulol synthesis. Moreover, a method for downregulating squalene synthesis based on Cu 2+ -repressible promoter was optimized, which significantly improved the patchoulol titer by 100.9% to 124 mg/L. In addition, a protein fusion strategy resulted in a final titer of 235 mg/L in shake flasks. Finally, 2.864 g/L patchoulol could be produced in a 5 L bioreactor, representing a remarkable 1684-fold increase compared to the baseline strain. To our knowledge, this is the highest patchoulol titer reported so far.

Facing the increasingly complex and deteriorated environment, people's thermal comfort and health requirements are expanding. Therefore, wearable materials with integrated functions have progressed rapidly due to the fair compatibility for various functions and precise regulation. In this work, a laminated MXene foam/cellulose@LDH composite membrane was fabricated via a facile process consisting of in situ growth, vacuum filtration, and foaming for asymmetrical personal thermal management and electromagnetic interference shielding. In detail, the Zn-Al LDH side shows a high solar reflectance of 0.89 and an infrared emissivity of 0.97 in the atmospheric window, demonstrating the superior radiative cooling property. In contrast, the outstanding radiative warming performance is revealed by the high solar absorption (0.72) and infrared reflectivity (0.55) of the MXene foam. As a result, prominent temperature differences were achieved during the validation test. Compared to the control group, an 18 °C reduction of the Zn-Al LDH side and a 9.6 °C increment of the MXene foam side were observed, bringing out the excellent optical properties and radiative thermal management performances. What is more, due to the outstanding electrical conductivity of MXene, a rapid and prominent temperature rise to 44.2 °C could be expected by applying a low voltage of 1 V to provide active joule warmth. In addition, hydrophobization and the associated stain resistance were explained by the high water contact angles of obtained membranes. The excellent electromagnetic interference shielding performance (43.9 dB) given by the introduction of MXene provides a prospective candidate to replace the common shielding materials. The results, in general, provide a promising strategy for meeting the updating requirements for comfortable living in a world full of potential thermal and health threats.

Oleic acid is widely applied in the chemical, material, nutritional, and pharmaceutical industries. However, the current production of oleic acid via high oleic plant oils is limited by the long growth cycle and climatic constraints. Moreover, the global demand for high oleic plant oils, especially the palm oil, has emerged as the driver of tropical deforestation causing tropical rainforest destruction, climate change, and biodiversity loss. In the present study, an alternative and sustainable strategy for high oleic oil production was established by reprogramming the metabolism of the oleaginous yeast Yarrowia lipolytica using a two-layer "push-pull-block" strategy. Specifically, the fatty acid synthesis pathway was first engineered to increase oleic acid proportion by altering the fatty acid profiles. Then, the content of storage oils containing oleic acid was boosted by engineering the synthesis and degradation pathways of triacylglycerides. The strain resulting from this two-layer engineering strategy produced the highest titer of high oleic microbial oil reaching 56 g/L with 84% oleic acid in fed-batch fermentation, representing a remarkable improvement of a 110-fold oil titer and 2.24-fold oleic acid proportion compared with the starting strain. This alternative and sustainable method for high oleic oil production shows the potential of substitute planting.

Escherichia coli BL21 (DE3) is the most widely used host for recombinant protein expression. However, not every protein can be highly expressed in BL21 (DE3), so individual optimization strategies are often required for different proteins, which is time-consuming and difficult to apply rapidly for industrial production. Constructing more hosts is a good choice to enrich protein expression selection. The expression level of T7 RNAP is the core control node of the pET expression system, so regulating its expression level is an effective way of improving the production of difficult-to-express proteins. Various BL21 (DE3)-derived variant hosts with different translation levels of T7 RNAP could be obtained by changing the ribosomal binding site (RBS) sequences of T7 RNAP in a genome. Here, a BL21 (DE3)-derived variant strain library with different RBS sequences of T7 RNAP was constructed using a base editor and CRISPR-Cas9. Notably, the CRISPR-Cas9 system combined with degenerate primers enabled the construction of an RBS library with 87.5% of the theoretical coverage in single editing, which is more convenient and efficient than the use of a base editor. The expression level of a target gene in the variant strain library ranged from 28 to 220% of the parental strain. Furthermore, a high-throughput host-screening platform for recombinant protein production was constructed, which enabled us to obtain the best expression host for certain target proteins in only 3 days. As a proof of concept, the production of all eight difficult-to-express proteins was greatly improved, including autolytic protein, membrane proteins, antimicrobial peptides, and hardly soluble proteins. Among them, the expression of glucose dehydrogenase in the best host exhibited a 298-fold increase compared to the parental strain. This strategy is simple and effective, requires no advanced equipment, and can be carried out in any laboratory.

The sesquiterpene α-humulene has been shown to have anti-inflammatory and anticancer activities, which has led to its vast application potential in medicine. However, α-humulene production methods including phytoextraction and chemical synthesis currently were limited to low yield, high costs, and expensive catalysts, which cannot meet the increasing market demand. In this study, Yarrowia lipolytica was developed as a robust cell factory for α-humulene production. The peroxisome in Y. lipolytica was first engineered to boost the synthesis of the sesquiterpene α-humulene. By compartmentalization of the α-humulene biosynthesis pathway, improving ATP and acetyl-CoA supply, and optimizing the gene copy numbers of rate-limiting enzymes, the engineered strain GQ2012 could produce 3.2 g/L α-humulene in a 5 L bioreactor, the highest α-humulene titer reported so far. Our study provides a valuable reference for highly sustainable production of terpenoids by peroxisome engineering in Y. lipolytica .

The filamentous fungus Fusarium fujikuroi is well-known for its production of natural plant growth hormones: a series of gibberellic acids (GAs). Some GAs, including GA1, GA3, GA4, and GA7, are biologically active and have been widely applied in agriculture. However, the low efficiency of traditional genetic tools limits the further research toward making this fungus more efficient and able to produce tailor-made GAs. Here, we established an efficient CRISPR/Cas9-based genome editing tool for F. fujikuroi. First, we compared three different nuclear localization signals (NLS) and selected an efficient NLS from histone H2B (HTB NLS ) to enable the import of the Cas9 protein into the fungal nucleus. Then, different sgRNA expression strategies, both in vitro and different promoter-based in vivo strategies, were explored. The promoters of the U6 small nuclear RNA and 5S rRNA, which were identified in F. fujikuroi, had the highest editing efficiency. The 5S rRNA-promoter-driven genome editing efficiency reached up to 79.2%. What's more, multigene editing was also explored and showed good results. Finally, we used the developed genome editing tool to engineer the metabolic pathways responsible for the accumulation of a series GAs in the filamentous fungus F. fujikuroi, and successfully changed its GA product profile, from GA3 to tailor-made GA4 and GA7 mixtures. Since these mixtures are more efficient for agricultural use, especially for fruit growth, the developed strains will greatly improve industrial GA production.

As compared to the traditional solid Janus particles, the hollow Janus particles have inspired growing interests due to their diverse potential applications. Herein, the novel hollow Janus particles with elephant trunk-like and acorn-like shapes were prepared by seed emulsion polymerization. In contrast to traditional template methods, the hollow structure was obtained during the preparation by one-step swelling method. The shapes and internal structures of hollow Janus particles were confirmed, and the compositions were identified too. Some critical influences on the morphology control were investigated, that is, the surface modification, the amount of surfactant, and cross-linking agent concentrations. It was inferred that the balance of hydrophilicity and hydrophobicity and the effective phase separation were important for preparing the hollow Janus particles with tailored shapes. Finally, amphiphilic properties of hollow Janus particles were demonstrated by emulsifying oil-water mixture.