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We propose a bidirectional controlled teleportation scheme using two pairs of Bell states as quantum channels. This solution uses Charlie as the controlled party. After two Bell state measurements, while Alice sends any single particle state to Bob, Bob can also send any single particle state to Alice, thus successfully completing the bidirectional controlled teleportation. Our plan is also compared with several other protocols from five aspects to illustrate that the plan has certain advantages. This makes our scheme relatively simpler and easier to implement and more maneuverable.

Comparative plastomics approaches have been used to identify available molecular markers for different taxonomic level studies of orchid species. However, the adoption of such methods has been largely limited in phylogeographic studies. Therefore, in this study, Dendrobium huoshanense, an endangered species with extremely small populations, was used as a model system to test whether the comparative plastomic approaches could screen available molecular markers for the phylogeographic study. We sequenced two more plastomes of D. huoshanense and compared them with our previously published one. A total of 27 mutational hotspot regions and six polymorphic cpSSRs have been screened for the phylogeographic studies of D. huoshanense. The cpDNA haplotype data revealed that the existence of haplotype distribution center was located in Dabieshan Mts. (Huoshan). The genetic diversity and phylogenetic analyses showed that the populations of D. huoshanense have been isolated and evolved independently for long period. On the contrary, based on cpSSR data, the genetic structure analysis revealed a mixed structure among the populations in Anhui and Jiangxi province, which suggested that the hybridization or introgression events have occurred among the populations of D. huoshanense. These results indicated that human activities have played key roles in shaping the genetic diversity and distributional patterns of D. huoshanense. According to our results, both two markers showed a high resolution for the phylogeographic studies of D. huoshanense. Therefore, we put forth that comparative plastomic approaches could revealed available molecular markers for phylogeographic study, especially for the species with extremely small populations.

La0.8Ce0.2Mn0.6Ni0.4O3 with (LCMN@CuO) and without (LCMN) CuO addition are prepared by solution methods, followed by reduction in 5% H2–N2 stream at 650 °C to form Ni exsolved and CuO reduced catalysts, LCMN@Ni and LCMN@Ni/Cu, for ethanol (EtOH) steam reforming (ESR). The catalysts are characterized by X-ray diffraction (XRD), scanning and transmission electron microscopies (SEM and TEM), temperature programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy etc., and are evaluated for ESR with a steam/carbon ratio of 3 and a weight hourly space velocity (WHSV) of 4 h−1 at temperatures between 500 and 700 °C. Ni exsolution and CuO reduction are confirmed on the substrates in LCMN@Ni and LCMN@Ni/Cu. Both the catalysts demonstrate a complete conversion of EtOH, forming mainly H2, CO2, CO and CH4. And increasing temperature to 700 °C increases the yields of H2 and CO to the levels about 90% and 40%, respectively, at the cost of CH4; and such performance remains unchanged for 30 h. These results indicate that both LCMN@Ni and LCMN@Ni/Cu are promising catalysts for ESR, the main difference between them is that the latter is more chemically stable and more resistant to carbon deposition under ESR conditions.

Most landslides induced by reservoir impoundment and rainfall in the Three Gorges Reservoir area of China are usually characterized by bedding-plane shear zones. This paper presents an experimental study of the interaction between water and shear-zone materials. A series of tests, including wetting-drying cycles and soaking tests, were carried out. The results show that the fluid-solid interaction not only reduces the shear strength of shear-zone soil but also accelerates the disintegration process of clastic rock from shear zone. After the fluid-solid interaction at different pH values, the clastic rock samples produce the most clay minerals in acidic solution. Similarly, the clay minerals of shear-zone soil samples increase dramatically after 45 days of soaking in acidic environment. According to the tests, it is found that the shear-zone soil in eluvium may originate from the weathered clastic rock near the shear zones under long-term fluid-solid interaction.

Introduction The Epimedium herb, Yinyanghuo in Chinese, is a famous Chinese herbal medicine. In this study, an efficient extraction method was developed for the extraction of major bioactive constituent epimedin A, epimedin B, epimedin C and icariin from E. pubescens Maxim. using deep eutectic solvents (DESs). Methodology A series of choline chloride-based DESs were synthesised for the extraction of four target compounds. DES composed of lactic acid and choline chloride with the ratio of 2:1 was selected as the most promising. Three vital factors affecting the extraction yields including water content, volume of DES aqueous solution and extraction time were optimised systematically by Box-Behnken experimental design in combination with response surface methodology. A high-performance liquid chromatography ultraviolet (HPLC-UV) method was developed for the sensitive and accurate quantification. Results The optimal extraction conditions were obtained as follows: water content of 17.5% (v/v), volume of DES aqueous solution 3.14 ml, and extraction time of 21 min. Under the optimal extraction conditions, the developed DES method could supply almost the same extraction yield as 50% ethanol, which were 98%, 99%, 97%, 96% for epimedin A, epimedin B, epimedin C and icariin, respectively. Conclusion The present study exhibited high efficiency in extraction of prenylflavonol glycosides in E. pubescens Maxim. Thus, DESs could be used as an alternative for efficient extraction and quantification of biologically active components from natural medical plants.

Although numerous in vitro studies have shown that osmolytes are capable of stabilizing proteins, their effect on protein folding in vivo has been less understood. In this work, we investigated the effect of osmolytes, including glycerol, sorbitol, betaine, and taurine, on the folding of a protein GB3 variant in E. coli cells using NMR spectroscopy. 400 mM osmolytes were added to E. coli cells; only glycerol stabilizes the folded protein, whereas betaine and taurine considerably destabilize the protein through modulating folding and unfolding rates. Further investigation indicates that betaine and taurine can enhance the quinary interaction between the protein and cellular environment and manifestly weaken the electrostatic attraction in protein salt bridges. The combination of the two factors causes destabilization of the protein in E. coli cells. These factors counteract the preferential exclusion mechanism that is adopted by osmolytes to stabilize proteins.

We have determined the interaction strengths of the common naturally occurring amino acids using a complete binding affinity matrix of 20 × 20 pairs of homo-octapeptides consisting of the 20 common amino acids between stationary and mobile states. We used a bead-based fluorescence assay for these measurements. The results provide a basis for analyzing specificity, polymorphisms, and selectivity of inter-amino-acid interactions. Comparative analyses of the binding energies, i.e., the free energies of association (ΔGA), reveal contributions assignable to both main-chain-related and side-chain-related interactions originating from the chemical structures of these 20 common amino acids. Side-chain–side-chain and side-chain–main-chain interactions are found to be pronounced in an identified set of amino acid pairs that determine the basis of inter-amino-acid recognition., Interaction strengths between common amino acids were measured with a bead-based fluorescence assay. The results provide a basis for analyzing specificity and selectivity of inter-amino-acid recognition.

In this study, a covalent organic framework designated as TpPaNO2 was synthesized by a mechanochemical grinding method and then coated on stainless steel wire by a sol-gel technique to prepare a solid-phase microextraction fiber. The TpPaNO2 fiber based solid-phase microextraction coupled with gas chromatography-electron capture detection was applied to determine the residues of 11 pesticides (trlfuralln, dicofol, α-endosulfan, 1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene, nitrofen, β-endosulfan, 1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethyl]benzene, 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane, bifenthrin, permethrin and fenvalerate) in vegetable and fruit samples. The effects of extraction time, extraction temperature, sample pH, stirring rate and desorption temperature on the extraction efficiency were investigated. Under the optimized conditions, the limits of detection for the eleven pesticides were in the range of 0.04-0.25 μg/kg. The recoveries of the eleven pesticides in the vegetable and fruit samples were 81.5-111% with the relative standard deviations less than 11.2%.

Headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry was adopted for the simultaneous determination of seven chlorophenols (CPs) from honey and canned-yellow-peach samples. A covalent organic framework made of 1,3,5-triformylphloroglucinol (Tp) and benzidine (BD) was used as the SPME fiber coating to preconcentrate the acetylation derivatives of the CPs. The main experimental parameters including derivatization conditions, extraction temperature and time, headspace volume, salt concentration, and desorption temperature were investigated. The fiber showed a high extraction capability for the CPs. The limits of detection (LODs) for the analytes were 0.3-0.7 μg kg

Inclined pile foundations are widely used in civil engineering by virtue of sufficient horizontal stiffness, but few studies have touched upon the seismic performance of inclined piles in liquefiable soil. To better understand the performance of the inclined piles in liquefiable soil under earthquake conditions, a series of 1 g shaking table tests of inclined and vertical piles in liquefiable soil were performed. Superstructure-pile-soil dynamic interaction was considered while three types of earthquake waves with different characteristics were selected as the applied earthquake motions. The horizontal acceleration of the superstructure and the pile cap, the rotational acceleration of the pile cap, the total base shear force, and the bending moment of two types of physical models were monitored and analyzed. The results show that inclined piles in liquefiable soil can effectively reduce the horizontal vibration of the superstructure and the pile cap, and the acceleration reduction of the pile cap is about 2.5 times larger than that of the superstructure. Meanwhile, inclined piles can also reduce the total base shear force, and the extent of reduction depends on the input earthquake wave. Besides, the results suggest that the maximum bending moment of inclined piles is located at the pile head, and its value is positively correlated with the amplitude of the earthquake wave, and is affected by the type of the input earthquake wave. Overall, inclined pile foundations show satisfactory seismic performance for a superstructure-foundation-liquefiable soil system, and this study, with a rich amount of data, can serve as an important reference for the seismic design of inclined piles in liquefiable soil.

Chinese bayberry leaves proanthocyanidins (BLPs) belongs to the prodelphinidin category with potent EGCG unit, whose inhibition effect on α-amylase and their interaction were investigated by in vitro digestion and enzyme kinetic analysis, multi fluorescence spectroscopies (fluorescence quenching, synchronous fluorescence, and three-dimensional fluorescence), circular dichroism spectra, Fourier transform infrared spectroscopy and in silico modelling. The results revealed that BLPs was a mixed inhibitor to α-amylase with the IC50 value of 3.075 ± 0.073 μg/mL. BLPs could lead to a static fluorescence quenching of α-amylase, mainly by means of interacting with amino acids (mainly Try and Tyr residues) in one site on α-amylase molecule under the action of hydrogen bonding and/or Van der Waals force. This interaction further induced the change of secondary conformational structure, functional group structure and hydrophobicity of α-amylase, thus resulting in lowering activity. Molecular docking simulated that this binding occurred in a cavity on the surface of the α-amylase molecule, and BLPs trimer showed a relatively high binding energy. The present study provided a new insight of BLPs as an α-amylase inhibitor, which could be considered in anti-diabetic therapy.

A solid-phase microextraction with carbon nanospheres coated fiber coupled with gas chromatographic detection was established for the determination of eight polycyclic aromatic hydrocarbons (naphthalene, biphenyl, acenaphthene, fluorine, phenanthrene, anthracene, fluoranthene, and pyrene) in water and soil samples. The experimental parameters (extraction temperature, extraction time, stirring rate, headspace volume, salt content, and desorption temperature) which affect the extraction efficiency were studied. Under the optimized conditions, good linearity between the peak areas and the concentrations of the analytes was achieved in the concentration range of 0.5-300 ng/mL for water samples, and in the concentration range of 6.0-2700 ng/g for soil samples. The detection limits for the analytes were in the range of 0.12-0.45 ng/mL for water samples, and in the range of 1.53-2.70 ng/g for soil samples. The method recoveries of the polycyclic aromatic hydrocarbons for spiked water samples were 80.10-120.1% with relative standard deviations less than 13.9%. The method recoveries of the analytes for spiked soil samples were 80.40-119.6% with relative standard deviations less than 14.4%. The fiber was reused over 100 times without a significant loss of extraction efficiency.

The metal detoxification mechanism is essential for the accumulation activity of some polychaetes. In order to investigate the detoxification function of metalloprotein II in polychaete Perinereis aibuhitensis, a recombinant fusion protein of MP II was successfully expressed in vitro and an anti-MP II polyclonal antibody was got. The tissue distribution of MP II in P. aibuhitensis and the protein expression under Cd, Pb and Zn exposure were detected by ELISA with this antibody. The results showed that MP II was higher in the intestine of P. aibuhitensis, followed by the body wall and parapodium. Cd, Zn and Pb exposure can induced MP II expression, but the change trend of MP II under various heavy metal exposure was different. The amount of MP II induced in P. aibuhitensis increased with the rises of Cd concentration, but there is no significant relationship between Zn and Pb concentration and MP II level.

A functionalized covalent organic framework (COF) was synthesized via room-temperature solvent-free mechano-chemical grinding method and used as a solid-phase extraction adsorbent for the extraction of eight biogenic amines (tryptamine, n-butylamine, phenylethylamine, cadaverine, putrescine, tyramine, spermine, and spermidine) in diverse meat samples. The target biogenic amines were derived with dansyl chloride to form stable fluorogenic derivatives for their high-performance liquid chromatography–fluorescence detection. The main important experimental parameters were investigated and optimized by both one-factor-at-a-time and response surface methodologies. Under the optimum conditions, a linear response for the biogenic amines was observed in the concentration range of 5.0–800.0 μg L−1 with the coefficients of determination (r2) ranging from 0.9944 to 0.9981. The limits of detection of this method (at a signal-to-noise ratio of 3) for the analytes ranged from 0.92 to 2.57 μg L−1. The method recoveries of the target biogenic amines for five meat samples ranged from 80.3 to 115%, with relative standard deviations lower than 12%. The results indicate that the prepared COF is an effective adsorbent for the enrichment of biogenic amines.

Lotus leaf flavonoids (LLF) are a group of bioactive natural substances. In this study, the structure, thermal properties, rheology behaviors and in vitro digestibility of cooked LLF-starch complex were investigated. Differential scanning calorimetry (DSC) analysis showed the shift in gelatinization peak to a higher temperature and the decrease in gelatinization enthalpies in the complexes significantly. The short-term retrogradation was retarded either. The flow behaviors of starch pastes changed with adding LLF. Scanning electron microscope (SEM) images showed a less compact structure in LLF-starch complex and laser confocal scanning microscope (CLSM) images detected that LLF mostly distributed around starch granules, which further prove the binding between LLF and starch. Moreover, fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) elucidated LLF probably interacted with starch by non-covalent bond especially hydrogen bond. In addition, LLF-starch complex exhibited inhibitory effect on starch digestion compared to pregelatinized starch, and the reasonable content of LLF-starch complex was (0.7 g/100 g). Thus, LLF-starch complex can be potentially used as a functional additive for high resistant starch (RS) and low glycemic index (GI) diets.

Multifunctional nanoplatforms for imaging‐guided synergistic antitumor treatment are highly desirable in biomedical applications. However, anticancer treatment is largely affected by the pre‐existing hypoxic tumor microenvironment (TME), which not only causes the resistance of the tumors to photodynamic therapy (PDT), but also promotes tumorigenesis and tumor progression. Here, a continuous O2 self‐enriched nanoplatform is constructed for multimodal imaging‐guided synergistic phototherapy based on octahedral gold nanoshells (GNSs), which are constructed by a more facile and straightforward one‐step method using platinum (Pt) nanozyme‐decorated metal–organic frameworks (MOF) as the inner template. The Pt‐decorated MOF@GNSs (PtMGs) are further functionalized with human serum albumin‐chelated gadolinium (HSA‐Gd, HGd) and loaded with indocyanine green (ICG) (ICG‐PtMGs@HGd) to achieve a synergistic PDT/PTT effect and fluorescence (FL)/multispectral optoacoustic tomography (MSOT)/X‐ray computed tomography (CT)/magnetic resonance (MR) imaging. The Pt‐decorated nanoplatform endows remarkable catalase‐like behavior and facilitates the continuous decomposition of the endogenous H2O2 into O2 to enhance the PDT effect under hypoxic TME. HSA modification enhances the biocompatibility and tumor‐targeting ability of the nanocomposites. This TME‐responsive and O2 self‐supplement nanoparticle holds great potential as a multifunctional theranostic nanoplatform for the multimodal imaging‐guided synergistic phototherapy of solid tumors., In this research, a tumor environment (TEM)‐responsive and continuous O2 self‐enriched drug delivery platform based on octahedral gold nanoshells (GNSs) using Pt‐decorated metal–organic frameworks (MOF) as inner template is constructed. The obtained nanostructures are further functionalized with human serum albumin‐gadolinium hybrid (HSA‐Gd, HGd) and loaded with indocyanine green (ICG) (ICG‐PtMGs@HGd) to achieve a multimodal imaging guided enhanced photodynamic therapy/photothermal therapy PDT/PTT effect.

A series of Cu x O self-assembled mesoporous microspheres (SMMs), with different and controlled morphology (virus-like, urchin-like, spherical), were synthesized by facile liquid phase approach. The morphology of the as-prepared Cu x O SMMs was evolved from spherical to virus-like shape by controlling the ratio of DI water in solution. It can also realize the transformation from loose assembly to dense assembly by extending the reaction time. These Cu x O SMMs exhibited good response to NO2 gas at room temperature, benefiting from their 3D self-assembly structure. Among these the resulting virus-like CuxO SNMMs-based sensor exhibits largely enhanced response to 1 ppm NO2 gas at room temperature. The enhanced response of the virus-like Cu2O SMMsbased sensor can be ascribed to the high surface area, hierarchical 3D nanostructures, micropores for effective gas diffusion, the heterojunctions formed between CuO and Cu2O, and the existence of abundant surface oxygen vacancies.

Due to the misuse of hormones and antibiotics resulting in drug residues in meat products, serious concerns have arisen regarding to the potential risks for human health. In this paper, a simple and efficient method was developed to simultaneously quantify six steroid hormones and six antibiotics in fatty foods by combining pressurized liquid extraction (PLE) with ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Adsorbents, extraction temperature, extraction time, recycle time and several other parameters were optimized in current investigation. The optimized PLE method was employed by using n-hexane-methanol-acetonitrile (2:1:1, v/v/v) as extraction solvent, silica gel as lipid sorbent, and the optimum parameters were 60 °C, 1500 psi and 10 min, respectively. Under the optimal conditions, the recoveries of spiked samples ranged from 82.2% to 115.0%. The limits of quantifications (LODs) were from 0.4 to 25.0 μg/kg. The developed PLE method was successfully applied to analyze steroid hormones and antibiotics in 27 fatty foods of hotpot ingredients without any additional clean-up steps. The results showed that the residues of estradiol benzoate (EB) and enrofloxacin (EN) in some matrices were much higher than maximum residue limits (MRLs) value, especially EB in fish, which exceeded 176.7 μg/kg. The results demonstrated that the developed method was sensitive and efficient in testing hotpot ingredients, and was an excellent analytical tool for monitoring residues of steroid hormones and antibiotics in fatty foods.

A fibrous magnetic boron nitride nanocomposite was synthesized and is shown to be a viable adsorbent for the magnetic solid phase extraction of pesticides prior to their quantitation by gas chromatography with electron capture detection. The optimum conditions were obtained by both single factor optimization and response surface analysis (Box-Behnken design). Under the optimized conditions, the response to the ten pesticides (dicofol, α-endosulfan, p,p’-DDE, nitrofen, β-endosulfan, p,p’-DDD, p,p’-DDT, bifenthrin, permethrin and fenvalerate) is linear in the 0.03–40 ng·mL−1 concentration range with the coefficients of determination ranging from 0.9970 to 0.9992. The relative standard deviations at concentration levels of 0.5 ng·mL−1, 20 ng·mL−1 and 40 ng·mL−1 were below 8.7%. The recoveries of the analytes from spiked tea water and tea beverage samples varied between 84.5% and 122%, with relative standard deviations ranging from 4.8 to 12%. The limits of detection are between 0.01 and 0.05 ng·mL−1. The adsorbent can be reused over 50 times without significant loss of extraction efficiency.

Understanding the hydration behavior of cereals during cooking is industrially important in order to optimize processing conditions. In this study, barley porridge was cooked in a sealed tin can at 100, 115, and 121 &deg, C, respectively, and changes in water uptake and hygroscopic swelling in dehulled barley grains were measured during the cooking of canned porridge. In order to describe and better understand the hydration behaviors of barley grains during the cooking process, a three-dimensional (3D) numerical model was developed and validated. The proposed model was found to be adequate for representing the moisture absorption characteristics with a mean relative deviation modulus (P) ranging from 4.325% to 5.058%. The analysis of the 3D simulation of hygroscopic swelling was satisfactory for describing the expansion in the geometry of barley. Given that the model represented the experimental values adequately, it can be applied to the simulation and design of cooking processes of cereals grains, allowing for saving in both time and costs.

The inhibition effect of three common proanthocyanidins (PA) on the retrogradation properties of maize starch was investigated (including grape seed proanthocyanidins (GSPA), peanut skin proanthocyanidins (PSPA), and pine bark proanthocyanidins (PBPA)). Differential scanning calorimetry (DSC) and X-ray diffraction (XRD) analysis showed that PA could significantly decrease the values of melting enthalpy of retrogradation (ΔHr) and the degree of relative crystallinity, suggesting that the starch re-crystallization was retarded by PA. Scanning electron microscope (SEM) characterizations illustrated that retrograded PA-starch samples formed a looser matrix with less appearance of continuous flakes during storage. Overall, 0.5 %-2.0 % of three PAs exhibited suppression of starch retrogradation after 21-day cooling storage, mainly resulting from the PA-starch interaction. Among them, PSPA showed the most substantial inhibition effect on starch retrogradation, which might be attributed to its structural features. This study suggested that PA could be a new type of inhibitor to suppress starch retrogradation.

Small molecular gels (SMGs) have drawn much attention due to their unique properties which can be used in wide range of applications. In this work, the two-component hydrogels based on intermolecular interaction were prepared by the mixing appropriate ratios of melamine (M) and nitrilotriacetic acid (N) in pure water. These obtained hydrogels, which own a three-dimensional (3D) supramolecular structure, responded to several external stimuli such as temperature, pH and halogen ions. Otherwise, the two-component hydrogels mixed with M and N in organic-water mixtures were studied by calculating the Hansen Solubility Parameters of the solvents, a gelation range of the known two-component could be defined. The untested solvent lied in this known range might be gelled by M and N, which is a useful model to identify the gelation and the particular application of a suitable two-component hydrogels.

A novel multi-residue method was developed for the simultaneous analysis of tetracyclines and β-receptor agonists in chicken by coupling pressurized liquid extraction (PLE) with ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The parameters of PLE method was optimised, such as extraction solvents, extraction temperature and several other parameters. The performance of the method was assessed and compared to QuEChERS extraction and ultrasound assisted extraction, which were widely used for the chicken extraction. PLE method proved to be suitable for the determination of tetracycline and β-receptor agonists, showing high recoveries, in the range of 84.1–107.9% with relative standard deviation less than 20%. PLE provided low LODs for CHL, OX and TE which were 18.0, 42.0 and 54.0 ng/kg respectively. Additionally, matrix effect of the PLE method exhibited slight effect on all target drugs. However, both ultrasound assisted extraction and QuEChERS extraction exhibited low recoveries and high LODs. The results showed that the established PLE method could be applied to the multiresidue analysis of tetracyclines and β-receptor agonists in chicken to ensure the safety of our daily food supply.

In this study, we modeled the water absorption, softening and shear viscosity change kinetics of canned rice porridge during cooking as well as estimated the thermodynamic properties involved in hydration. Moreover, the internal microstructure of rice kernels was observed under different hydrothermal conditions. During cooking, the water absorption and shear viscosity alteration rate increased with temperature, whereas the softening rate decreased. However, the temperature did not significantly affect the equilibrium value of the physical properties. The variation tendencies of the moisture content and hardness of the kernels could be expressed satisfactorily by the exponential and the generalized exponential models. The porridge shear viscosity variations fitted the sigmoidal and its generalized models. Thermodynamic parameters (enthalpy, entropy and Gibbs free energy) revealed that the hydration process was non-spontaneous and exothermic. Furthermore, scanning electron microscopy images and the results of the X-ray diffraction analysis showed the microstructure of the kernels during cooking, and the kernels formed a homogeneous mesh structure at earlier times during the initial stage at higher temperatures. These findings would provide valuable information for the optimization of canned rice porridge production.

Background G-protein-coupled receptors (GPCRs) are one of the most important molecules that transfer signals across the plasma membrane, and play central roles in physiological systems. The molecular architecture of GPCRs allows them to bind to diverse chemicals, including environmental contaminants. Methods To investigate the effects of benzo(a)pyrene (B(a)P) on GPCR signaling, GPCR and the protein kinase A (PKA) catalytic subunit of Perinereis aibuhitensis were cloned. The expression patterns of these two genes during B(a)P exposure were determined with real-time fluorescence quantitative PCR. The PKA content in P. aibuhitensis under B(a)P exposure was examined. Results The full-length cDNAs of PaGPCR and the PaPKA catalytic subunit were 1,514 and 2,662 nucleotides, respectively, encoding 338 and 350 amino acids, respectively. Multiple sequence alignments indicated that the deduced amino acid sequence of PaGPCR shared a low level of similarity with the orphan GPCRs of polychaetes and echinoderms, whereas PaPKA shared a high level of identify with the PKA catalytic subunits of other invertebrates. B(a)P exposure time-dependently elevated the expression of PaGPCR and PaPKA. The expression of both PaGPCR and PaPKA was also dose-dependent, except at a dose of 10 μg/L B(a)P. The PKA content in concentration group was elevated on day 4, with time prolonging the PKA content was down-regulated to control level. Discussion These results suggested that GPCR signaling in P. aibuhitensis was involved in the polychaete’s response to environmental contaminants.