Cis Form Research Articles

1,2-BF2 Shift and Photoisomerization Induced Multichromatic Response.

Adaptive materials that exhibit a multichromatic response as a function of applied stimulus are highly desirable, as they can result in applications ranging from smart surfaces to anticounterfeit devices. Here we report on such a system based on an intriguing thermal 1,2-BF2 shift that transforms a visible-light-activated azo-BF2 photoswitch into a BF2-hydrazone fluorophore (BODIHY) in both solution and the solid-state. Structure-property analysis, in conjunction with DFT calculations, reveals that the shift is catalyzed by the spatial proximity of an oxygen atom next to the BF2 group and that the activation originates from an electronic and not steric effect. Theoretical calculations also show that while the energy barrier for the trans → BODIHY transformation is accessible at room temperature (thermal half-life of 30 h), the cis → BODIHY transformation has a much higher barrier, which is why the 1,2-BF2 shift is not observed for the cis form. The photoswitching of the azo-BF2, in conjunction with the 1,2-BF2 shift, was then used in the multicolor modulation of a switch-containing cross-linked polydimethylsiloxane film using light and/or heat stimuli, elaborating the usefulness of the sophisticated reaction cascade that can be accessed from this simple system.

Experimentally Histological Assessment for the Effect of Resveratrol in the Liver of Mice

Resveratrol a major Polyphenolic compound is a non-flavonoid stilbene, was isolated and purified as a first time in Iraq from the skin of black grape had grown in this country. Many studies confirmed the biological importance of this substance in different disorders, beside the protective properties specially towered the hepatic cells against free radicals and drugs toxic effects as histological level. In this study the purified resveratrol from Iraqi black grape was administered to groups of normal mice in three doses to investigate if there is any unwanted or harmful effects which may appear on the mice liver after fifteen days and thirty days administrated as intrapretoneal single dose a day Results showed that the extraction method estimated resveratrol in two stereo isomer mixture cis and trance forms. The different doses within two intervals affected the hepatocytes in different manner. The harmful properties of this substance appeared to be more potent in relation with dose and exposure time increasing. The study concluded that there must be an extensive studies that bridge the gap of available information with what is required regarding the Iraqi purified resveratrol as a safe therapeutic substance, not only for treating liver disorders, but in all it's therapeutic purposes

Evaluation of Plant Essential Oils as Natural Alternatives for Alcohol-based Mouthwashes: Spotlight—Lemongrass and Citronella Java

Abstract Objective The purpose of our study was to evaluate plant-derived essential oils (EOs) as natural alternatives to commercial alcohol-based mouthwashes in the prevention of dental caries since several recent studies have linked high incidence of oral cancer among users with a history of prolonged use of alcohol-based mouthwashes. Materials and Methods Lemongrass, Citronella Java, Gingergrass, and Caraway seed EOs were tested against commonly occurring multidrug-resistant (MDR) oral bacteria namely Micrococcus luteus, Enterococcus faecalis, Streptococcus oralis, and Streptococcus salivarius. Agar well diffusion method was used to determine the antibacterial effectiveness of these EOs. Samples of Citronella Java and Lemongrass EO were also analyzed by gas chromatography (GC). Results Lemongrass and Citronella Java exhibited the highest antibacterial activity against all four bacterial strains. Inhibition zones of Lemongrass were 12, 21.3, 28.3, and 32 mm in diameter against E. faecalis, M. luteus, S. oralis, and S. salivarius, respectively. In comparison, inhibition zones of Citronella Java were 11.5, 17, 20.7, and 20.2 mm in diameter against E. faecalis, M. luteus, S. oralis, and S. salivarius, respectively. A significant finding in our study was that antibacterial activity of Lemongrass was much higher than that of tetracycline, a broad-spectrum antibiotic, against S. oralis and S. salivarius, while the inhibitory effects of Citronella Java against these two oral streptococci were comparable to tetracycline. The major components of Citronella Java identified by GC were citronellal, citronellol, and geraniol, whereas Lemongrass was primarily composed of cis and trans forms of citral. Conclusion Our results suggest that Lemongrass and Citronella Java could be promising natural alternatives to alcohol-based mouthwashes against MDR oral bacteria in the prevention of dental caries.

Sequence effects on the thermal cis–trans isomerization of side‐chain stearate‐containing azobenzene polymers

AbstractPhotochromic azobenzenes undergo light‐mediated trans–cis isomerization. The cis isomer reverts to the trans isomer thermally. To investigate the effect of different monomer sequences on the thermal stability of cis‐azobenzene, a series of copolymers, namely, block, and random structures containing stearic acid and azobenzene moieties as their side chains have been synthesized through reversible addition–fragmentation chain transfer (RAFT) polymerization. In this study, we investigate the photoisomerization of the trans and cis forms of the polymers and also the thermal reversal of the cis‐azobenzene photochromic systems. The isomerization data revealed significant differences in the isomerization timescales between the polymers and the corresponding monomer. It was observed that the local polarity around the azobenzene units within a polymer was significantly influenced by the chain segment depending on whether it was in the vicinity of the hydrophobic alkyl chains or other azobenzene units. This local environment of the azobenzene units regulates the stabilization of the transition states during the cis–trans thermal isomerization, consequently affecting the half‐life of the cis isomer.

Ultrafast Raman observation of the perpendicular intermediate phantom state of stilbene photoisomerization.

Trans-cis photoisomerization is generally described by a model in which the reaction proceeds via a common intermediate having a perpendicular conformation around the rotating bond, irrespective of from which isomer the reaction starts. Nevertheless, such an intermediate has yet to be identified unambiguously, and it is often called the 'phantom' state. Here we present the structural identification of the common, perpendicular intermediate of stilbene photoisomerization using ultrafast Raman spectroscopy. Our results reveal ultrafast birth and decay of an identical, short-lived transient that exhibits a vibrational signature characteristic of the perpendicular state upon photoexcitation of the trans and cis forms. In combination with ab initio molecular dynamics simulations, it is shown that the photoexcited trans and cis forms are funnelled off to the ground state through the same, perpendicular intermediate.

On the third-order nonlinear optical responses of cis and trans stilbenes - a quantum chemistry investigation.

The second hyperpolarizabilities (γ) of the stilbene molecular switch in its trans and cis forms have been calculated using quantum chemistry methods to address their third-order nonlinear optical contrasts, to assess the reliability of lower-cost DFT methods, and to make comparisons with experiments. First, the reference CCSD(T) method shows that trans-stilbene presents a γ‖ value twice larger than its cis isomer (its γTHS value is 2.7 times larger). Among more cost-effective methods, reliable results are obtained at MP2 as well as with DFT, provided the CAM-B3LYP or ωB97X-D XCFs are employed. Supplementary DFT calculations have investigated the relationships between the accuracy of the exchange-correlation functionals, the fulfillment of Koopmans' theorem, and the delocalization error, and they demonstrated that satisfying Koopmans' theorem is not the condition for the best accuracy but that functionals with small delocalization errors are generally efficient. Using the selected CAM-B3LYP, large γ enhancements by about 70% (trans-stilbene) and 50% (cis-stilbene) have been evidenced when accounting for solvent effects using an implicit solvation model (IEFPCM), even for apolar solvents. Then, the frequency dispersion of the γ responses has been described using Bishop polynomial expansions, allowing comparisons with a broad set of experimental data. To a certain extent, no systematic agreement between the calculations and the measured values was found. On the one hand, the agreement is satisfactory for the γ(-ω;ω,-ω,ω) quantities, provided that the dominant vibrational contribution is taken into account. On the other hand, the agreement is poor for the γ(-2ω;ω,ω,0) and γ(-3ω;ω,ω,ω) quantities, while some inconsistencies between experimental values are also highlighted.

Searching low-energy conformers of neutral and protonated di-, tri-, and tetra-glycine using first-principles accuracy assisted by the use of neural network potentials.

In the last ten years, combinations of state-of-the-art gas-phase spectroscopies and quantum chemistry calculations have suggested several intuitive trends in the structure of small polypeptides that may not hold true. For example, the preference for the cis form of the peptide bond and multiple protonated sites was proposed by comparing experimental spectra with low-energy minima obtained from limited structural sampling using various density functional theory methods. For understanding the structures of polypeptides, extensive sampling of their configurational space with high-accuracy computational methods is required. In this work, we demonstrated the use of deep-learning neural network potential (DL-NNP) to assist in exploring the structure and energy landscape of di-, tri-, and tetra-glycine with the accuracy of high-level quantum chemistry methods, and low-energy conformers of small polypeptides can be efficiently located. We hope that the structures of these polypeptides we found and our preliminary analysis will stimulate further experimental investigations.

Solvent-polarity dependence of ultrafast excited-state dynamics of trans-4-nitrostilbene.

Ultrafast excited-state dynamics of the simplest nitrostilbenes, namely trans-4-nitrostilbene (t-NSB), was studied in solvents of various polarities with ultrafast broadband time-resolved fluorescence and transient absorption spectroscopies, and by quantum-chemical computations. The results revealed that the initially excited S1(ππ*) state deactivation dynamics is strongly influenced by the solvent polarity. Specifically, the t-NSB S1-state lifetime decreases by three orders of magnitude from ∼60 ps in high-polarity solvents to ∼60 fs in nonpolar solvents. The strong solvent-polarity dependence arises from the differences in dipole moments among the S1 and relevant states, including the major intersystem crossing (ISC) receiver triplet states, and therefore, the solvent polarity can modulate their relative energies and ISC rates. In nonpolar solvents, the sub-100 fs lifetime is due to a combination of efficient ISC and internal conversion. In medium-polarity solvents, the S1-state population decays via a competing ISC relaxation mechanism in a biphasic manner, and the ISC rates are found to obey the inverse energy gap law of the strong coupling case. In high-polarity solvents, the S1 state is stabilized to a much lower energy such that ISC becomes energetically infeasible, and the S1 state decays via barrier crossing along the torsion angle of the central ethylenic bond to the nonfluorescent perpendicular configuration. Regardless of the initial S1-state deactivation pathways in various solvents, the excited-state population is ultimately trapped in the metastable T1-state perpendicular configuration, at which a slower ISC occurs to bring the system to the ground state and bifurcate into either trans or cis form of NSB.

Isomerism of : Accurate structural, energetic, and spectroscopic characterization.

A recent work [Ye et al. Mon. Not. R. Astron. Soc. 2023, 525, 1158] on the gas-phase formation of t-HC(O)SH, already detected in the interstellar medium, pointed out that the trans form of HC(S)OH is a potential candidate for astronomical observations. Prompted by these results, the family of isomers has been investigated from an energetic point of view using a double-hybrid density functional in combination with a partially augmented triple-zeta basis set. This preliminary study showed that the most stable species of the family are the cis and trans forms of HC(O)SH and HC(S)OH. For their structural and spectroscopic characterization, a composite scheme based on coupled cluster (CC) calculations that incorporates up to the quadruple excitations and accounts for the extrapolation to the complete basis set limit and core correlation effects has been employed. This approach opens to the prediction of rotational constants with an accuracy of 0.1%. A hybrid scheme, based on harmonic frequencies computed using the CC singles, doubles and a perturbative treatment of triples method (CCSD(T)) in conjunction with a quadruple-zeta basis set, allowed us to obtain fundamental vibrational frequencies with a mean absolute error of about 1%.

Study of structural characteristics and charge distribution in pyranocoumarins: A computational approach

Fourteen pyranocoumarin (PC) molecules having cis and trans conformations are studied for charge distribution patterns with the help of computational study. To understand the structural characteristics of these molecules, global molecular descriptors, TD-DFT, and NLO studies are employed. On the basis of charge symmetry and MEP plots, it was predicted that trans PC would produce better outcomes. From the findings, it is evident that cis PC had less charge symmetry than trans PC. Although the electrophilicity index suggested the opposite pattern, the values for chemical potential, chemical hardness, and hyperhardness were higher for cis conformation than for trans conformation. Based on the data, it can be concluded that PC with a benzimidazole group exhibits higher intramolecular charge transfer in both its cis and trans forms. Compared to other pyranocoumarins, PC with no substituent clearly displayed weak inference.

Light responsive microstructural transitions in photo-responsive wormlike micelle mediated viscoelastic material based on cationic surfactant and photo-responsive organic acids

Designing smart materials with fine-tunable structures and stimuli-tunable characteristics within a single molecule is a challenging task for the scientific community. This kind of materials circumvent limitations of conventional materials and are applicable in the formation of soft robotics, actuators, tissue engineering, optical devices, molecular switches and biosensors. In our efforts to design photo-responsive materials, herein we have designed photo-responsive wormlike micelle mediated viscoelastic materials (WMMVMs) through the synergistic interactions between the cetyltrimethylammonium bromide (CTAB) with photo-responsive organic acids (P-OA), i.e.,trans-cinnamic acid (t-CA) and p-coumaric acid (p-CA). Upon exposing the WMMVMs to UV light of 270 nm, drastic drop in viscoelasticity was observed because of the conversation of wormlike micelles in to rodlike micelles as the P-OAs are transformed from its trans form to cis form, confirmed through rheology and SANS. Further, the morphology of the system before and after UV irradiation was confirmed through SEM and TEM images. The irreversible photo-responsive character of the P-OA contributed to the irreversible photo-responsive behavior of the investigated systems. These systems bear good rheological behavior; specifically, Maxwell behavior. Additionally, these viscoelastic materials are also having excellent stretchability (20 times than its original length), self-healing (2 min) ability and higher thermal stability (>262 0C). WMMVMs also exhibited pH (below pKa) and temperature induced (CTAB/t-CA and CTAB/p-CA at 42 °C and 40 °C, respectively) reversible change in viscoelastic properties. We believe that the studied WMMVMs can serve as a useful model in understanding the process of photo-responsiveness and in various applications.

Investigation of ultrafast photoisomerization dynamics of azobenzene derivative (E)-1-phenyl-2-((triisopropylsilyl)ethynyl)diazene

When exposed to light at a specific wavelength, azobenzene and its derivatives experience a transformation from trans form to cis form through isomerization. Due to its ability to change color upon illumination, azobenzene finds extensive use in various molecular devices and functional materials. However, despite significant researches focused on practical applications, there are still ongoing investigations into the underlying mechanisms governing azobenzene’s photochemical reactions and isomerization. In this study, we employ femtosecond stimulated Raman spectroscopy (FSRS), and transient absorption spectroscopy, in conjunction with quantum chemical calculations, to elucidate the ultrafast isomerization dynamics of an azobenzene derivative known as trans-AZOTIPS ((E)-1-phenyl-2-((triisopropylsilyl)ethynyl)diazene). The results demonstrate that upon photoexcitation, rapid isomerization occurs along the C−N=N bonds via the singlet excited state S1 to hot ground state (S0*) state transition. Additionally, we explore the impact of solvent viscosity on the isomerization process and find that the duration of isomerization remains unaffected by variations in solvent viscosity. These results suggest that the isomerization pathway involves a volume-conserving motion known as “hula twist”. After that, the vibrational cooling process is obtained in S0 state.

Photo-Controlled Gating of Selective Bacterial Membrane Interaction and Enhanced Antibacterial Activity for Wound Healing.

Reversible biointerfaces are essential for on-demand molecular recognition to regulate stimuli-responsive bioactivity such as specific interactions with cell membranes. The reversibility on a single platform allows the smart material to kill pathogens or attach/detach cells. Herein, we introduce a 2D-MoS2 functionalized with cationic azobenzene that interacts selectively with either Gram-positive or Gram-negative bacteria in a light-gated fashion. The trans conformation (trans-Azo-MoS2 ) selectively kills Gram-negative bacteria, whereas the cis form (cis-Azo-MoS2 ), under UV light, exhibits antibacterial activity against Gram-positive strains. The mechanistic investigation indicates that the cis-Azo-MoS2 exhibits higher affinity towards the membrane of Gram-positive bacteria compared to trans-Azo-MoS2 . In case of Gram-negative bacteria, trans-Azo-MoS2 internalizes more efficiently than cis-Azo-MoS2 and generates intracellular ROS to kill the bacteria. While the trans-Azo-MoS2 exhibits strong electrostatic interactions and internalizes faster into Gram-negative bacterial cells, cis-Azo-MoS2 primarily interacts with Gram-positive bacteria through hydrophobic and H-bonding interactions. The difference in molecular mechanism leads to photo-controlled Gram-selectivity and enhanced antibacterial activity. We found strain-specific and high bactericidal activity (minimal bactericidal concentration, 0.65 μg/ml) with low cytotoxicity, which we extended to wound healing applications. This methodology provides a single platform for efficiently switching between conformers to reversibly control the strain-selective bactericidal activity regulated by light.

Photo‐Controlled Gating of Selective Bacterial Membrane Interaction and Enhanced Antibacterial Activity for Wound Healing

AbstractReversible biointerfaces are essential for on‐demand molecular recognition to regulate stimuli‐responsive bioactivity such as specific interactions with cell membranes. The reversibility on a single platform allows the smart material to kill pathogens or attach/detach cells. Herein, we introduce a 2D‐MoS2 functionalized with cationic azobenzene that interacts selectively with either Gram‐positive or Gram‐negative bacteria in a light‐gated fashion. The trans conformation (trans‐Azo‐MoS2) selectively kills Gram‐negative bacteria, whereas the cis form (cis‐Azo‐MoS2), under UV light, exhibits antibacterial activity against Gram‐positive strains. The mechanistic investigation indicates that the cis‐Azo‐MoS2 exhibits higher affinity towards the membrane of Gram‐positive bacteria compared to trans‐Azo‐MoS2. In case of Gram‐negative bacteria, trans‐Azo‐MoS2 internalizes more efficiently than cis‐Azo‐MoS2 and generates intracellular ROS to kill the bacteria. While the trans‐Azo‐MoS2 exhibits strong electrostatic interactions and internalizes faster into Gram‐negative bacterial cells, cis‐Azo‐MoS2 primarily interacts with Gram‐positive bacteria through hydrophobic and H‐bonding interactions. The difference in molecular mechanism leads to photo‐controlled Gram‐selectivity and enhanced antibacterial activity. We found strain‐specific and high bactericidal activity (minimal bactericidal concentration, 0.65 μg/ml) with low cytotoxicity, which we extended to wound healing applications. This methodology provides a single platform for efficiently switching between conformers to reversibly control the strain‐selective bactericidal activity regulated by light.

Investigation of production mechanism, structure, and formulation of Se-methyl methaneselenoate and its halogen derivatives by density functional theory (DFT)

In this study, the production mechanism of Se-methyl methaneselenoate in the presence of carbon monoxide against copper oxide nanoparticles simulation and investigated its most stable structure have been. Configurational properties of Se-methyl methaneselenoate and its halogen derivatives are evaluated and investigated using density function theory (DFT).The calculation method results of LC-WPBE/6–311 + G** show that the stereoisomerism cis form of these compounds is more stable than their trans form. IRC calculations are used to determine the path of the reaction. The frequency calculations, thermodynamic and structure parameters, force and equilibrium constants are calculated for confirm the transition state and the most stability configuration. The anomeric property and electron transfer increase with the replacement of halogen instead of 5H. The highest amount of E(2)/kcal.mol−1 is for [Lp(2) O1 → π*(C2-Se3)] of cis form, in its halogenated compounds, it increases with the reduction in the electronegativity and increasing in the atomic radius of the halogen.

Determination of saturated fat, unsaturated fat, and trans fat in commercial instant noodles based on the analysis of fatty acid composition by gas chromatography

AbstractIn the food processing sector, it is crucial to identify the composition and fat content of items that have undergone heat‐processing. The total fat content is the primary factor used to determine the fat content of instant noodle products. As a result, a technique must be developed to identify fat content by determination of fatty acid composition, particularly trans fatty acids. In this study, we used the reliable GC‐FID/MS technique to analyze the methyl ester derivatives of 37 different kinds of fatty acids. The results showed that high saturated fat concentration in all samples was mostly palmitic acid, whereas the low unsaturated fatty acid content in the cis form was primarily oleic acid and linoleic acid. The amount of monounsaturated and polyunsaturated fats is quite low. Trans fat level was almost non‐existent in all samples. The amounts of palmitic acid and oleic acid in the samples ranged from 4.10% to 12.84% and 2.62% to 7.65%, respectively, as did linoleic acid and stearic acid. Monounsaturated and polyunsaturated fatty acid concentration ranged from 2.62% to 7.82% and 0.52 to 1.81%, respectively. The proportion of polyunsaturated fat to saturated fat was quite low. Therefore, it is essential to have procedures in place to keep an eye on the saturated fatty acid level, which has a negative impact on consumers' health. The findings of experimental research demonstrated that trans fatty acids were not present in instant noodle products. It revealed that the food processing sector has advanced favorably and catered to the demands of both the domestic and international markets.

Photochemistry of the Retinal Chromophore in Microbial Rhodopsins.

Microbial rhodopsins are photoreceptive membrane proteins of microorganisms that express diverse photobiological functions. All-trans-retinylidene Schiff base, the so-called all-trans-retinal, is a chromophore of microbial rhodopsins, which captures photons. It isomerizes into the 13-cis form upon photoexcitation. Isomerization of retinal leads to sequential conformational changes in the protein, giving rise to active states that exhibit biological functions. Despite the rapidly expanding diversity of microbial rhodopsin functions, the photochemical behaviors of retinal were considered to be common among them. However, the retinal of many recently discovered rhodopsins was found to exhibit new photochemical characteristics, such as highly red-shifted absorption, isomerization to 7-cis and 11-cis forms, and energy transfer from a secondary carotenoid chromophore to the retinal, which is markedly different from that established in canonical microbial rhodopsins. Here, I review new aspects of retinal found in novel microbial rhodopsins and highlight the emerging problems that need to be addressed to understand noncanonical retinal photochemistry.

Amide isomerization pathways: Electronic and structural background of protonation- and deprotonation-mediated cis-trans interconversions.

The cis-trans isomerization of amide bonds leads to wide range of structural and functional changes in proteins and can easily be the rate-limiting step in folding. The trans isomer is thermodynamically more stable than the cis, nevertheless the cis form can play a role in biopolymers' function. The molecular system of N-methylacetamide · 2H2O is complex enough to reveal energetics of the cis-trans isomerization at coupled cluster single-double and coupled cluster single-double and perturbative triple [CCSD(T)] levels of theory. The cis-trans isomerization cannot be oversimplified by a rotation along ω, since this rotation is coupled with the N-atom pyramidal inversion, requesting the introduction of a second dihedral angle "α." Full f(ω,α) potential energy surfaces of the different amide protonation states, critical points and isomerization reaction paths were determined, and the barriers of the neutral, O-protonated and N-deprotonated amides were found too high to allow cis-trans interconversion at room temperature: ∼85, ∼140, and ∼110 kJ mol-1, respectively. For the N-protonated amide bond, the cis form (ω = 0°) is a maximum rather than a minimum, and each ω state is accessible for less than ∼10 kJ mol-1. Here we outline a cis-trans isomerization pathway with a previously undescribed low energy transition state, which suggests that the proton is transferred from the more favorable O- to the N-protonation site with the aid of nearby water molecules, allowing the trans → cis transition to occur at an energy cost of ≤11.6 kJ mol-1. Our results help to explain why isomerase enzymes operate via protonated amide bonds and how N-protonation of the peptide bond occurs via O-protonation.

Conformational analysis of carboxylic acid anhydrides: A microwave and computational study

The microwave spectra of four carboxylic acid anhydrides, RCOOCOR′, (R,R′) = (CH3,CF3), (C(CH3)3,CF3), (C6H5, CF3) and (CH3, C(CH3)3), have been observed in a supersonic jet. Calculations at the M06-2X/6-311++G(d,p) and MP2/6-311++G(d,p) levels of theory predict the lowest energy conformations for all four species to be nonplanar cis structures, i.e., conformations in which the C=O groups point in approximately the same direction, but are twisted out of a coplanar orientation. The observed spectra are consistent with these predictions. In addition, for all but the (R,R′) = (CH3, C(CH3)3) species, higher energy nonplanar trans conformers are also predicted, typically within 1–2 kcal/mole the nonplanar cis form. For (R,R′)= (C(CH3)3, CF3), extensive isotopic substitution has enabled a determination of most of the (non-fluorine) heavy atom structural parameters. Excellent agreement with the DFT and MP2 structures was obtained, thus validating the theoretical methods used. A strong correlation is found between the calculated O=C⋯C=O dihedral angle and the average of the vapor phase C=O stretching frequencies of RCOOH and R′COOH.

Unveiling the Latest Breakthroughs in Menaquinone-7 Research through Fermentation-Based Production

MK-7, like other biological molecules, exists in geometric isomers, including cis and trans forms, among which only the all-trans form holds biological significance. Recent studies have drawn attention to the manifold health advantages linked to the consumption of menaquinone-7 (MK-7). Nonetheless, the scarcity of MK-7 in natural dietary sources underscores the necessity for creating dietary supplements to fulfil daily intake requisites. Obtaining MK-7 involves employing production techniques encompassing solid- or liquid-state fermentation. However, upscaling this process becomes intricate in static fermentation due to challenges in heat and mass transfer. Consequently, the bulk of research on MK-7 synthesis via fermentation has concentrated on the liquid-state approach. To this end, endeavors have been dedicated to refining MK-7 biosynthesis by exploring diverse fermentation media compositions, optimal growth conditions, and even integrating nanobiotechnology methodologies. Innovative biofilm reactors, capable of facilitating biofilm attachment on plastic composite substrates, have also emerged as a promising solution, particularly when utilizing B. subtilis cells. The biofilm reactors exhibit robust extracellular MK-7 secretion, effectively surmounting the hurdles posed by high aeration and agitation rates. However, a demonstration of the scalability of this technology to pilot and industrial scales is still pending. This work offers an outline of the latest advancements in MK-7 research, with a specific focus on the strides made in MK-7 production through fermentation techniques. The paramount importance of the all-trans form of MK-7 is underscored, accentuating its role in enhancing human well-being. The ramifications of this work hold the potential to pave the way for novel strategies to amplify MK-7 production and formulate products with an optimized MK-7 profile, thereby promising avenues for enhancing human health and nutrition.