This paper presents a very simple method to derive the explicit transformations of the optimal economical 1 to M phase-covariant cloning. The fidelity of clones reaches the theoretic bound [D＇Ar]ano G M and Macchiave...This paper presents a very simple method to derive the explicit transformations of the optimal economical 1 to M phase-covariant cloning. The fidelity of clones reaches the theoretic bound [D＇Ar]ano G M and Macchiavello C 2003 Phys. Rev. A 67 042306]. The derived transformations cover the previous contributions [Delgado Y, Lamata Let al, 2007 Phys. Rev. Lett. 98 150502] in which M must be odd.展开更多
In this paper, we derive the explicit transformations of the optimal 1→3, 4, 5 phase-covariant cloning in three dimensions, and then generalize them to the cases of 1 → M = 3n, 3n ＋ 1, 3n ＋ 2 （n ≥ 1 integer） cl...In this paper, we derive the explicit transformations of the optimal 1→3, 4, 5 phase-covariant cloning in three dimensions, and then generalize them to the cases of 1 → M = 3n, 3n ＋ 1, 3n ＋ 2 （n ≥ 1 integer） cloning. The clone fidelities are coincident with the theoretical bounds found.展开更多
We review the basic theory of approximate quantum cloning for discrete variables and some schemes for implementing quantum cloning machines. Several types of approximate quantum clones and their expansive quantum clon...We review the basic theory of approximate quantum cloning for discrete variables and some schemes for implementing quantum cloning machines. Several types of approximate quantum clones and their expansive quantum clones are intro- duced. As for the implementation of quantum cloning machines, we review some design methods and recent experimental results.展开更多
This paper proposes a scheme where one can realize quantum cloning of an unknown two-atom entangled state with assistance of a state preparer in cavity QED. The first stage of the scheme requires usual teleportation. ...This paper proposes a scheme where one can realize quantum cloning of an unknown two-atom entangled state with assistance of a state preparer in cavity QED. The first stage of the scheme requires usual teleportation. In the second stage of the scheme, with the assistance of the preparer, the perfect copies of an unknown atomic entangled state can be produced.展开更多
This paper proposes a scheme for the implementation of 1→ 3 optimal phase-covariant quantum cloning with trapped ions. In the present protocol, the required time for the whole procedure is short due to the resonant i...This paper proposes a scheme for the implementation of 1→ 3 optimal phase-covariant quantum cloning with trapped ions. In the present protocol, the required time for the whole procedure is short due to the resonant interaction, which is important in view of decoherence. Furthermore, the scheme is feasible based on current technologies.展开更多
Two quantum logic networks are proposed to simulate a cloning machine that copies the states near a given one. Probabilistie cloning based on the first network is realized and the cloning probability of success based ...Two quantum logic networks are proposed to simulate a cloning machine that copies the states near a given one. Probabilistie cloning based on the first network is realized and the cloning probability of success based on the second network is lOOe/0. Therefore, the second network is more motivative than the first one.展开更多
This paper presents a quantum network to implement the optimal 1→2 quantum cloning in 2 dimensions, including the optimal asymmetric universal, the optimal symmetric phase-covariant, and the asymmetric real state clo...This paper presents a quantum network to implement the optimal 1→2 quantum cloning in 2 dimensions, including the optimal asymmetric universal, the optimal symmetric phase-covariant, and the asymmetric real state cloning. By only choosing different angles of the single-qubit rotations, the quantum network can implement three optimal quantum cloning.展开更多
Quantum steering in a global state allows an observer to remotely steer a subsystem into different ensembles by performing different local measurements on the other part. We show that, in general, this property cannot...Quantum steering in a global state allows an observer to remotely steer a subsystem into different ensembles by performing different local measurements on the other part. We show that, in general, this property cannot be perfectly cloned by any joint operation between a steered subsystem and a third system. Perfect cloning is viable if and only if the initial state is of zero discord. We also investigate the process of cloning the steered qubit of a Bell state using a universal cloning machine. Einstein–Podolsky–Rosen(EPR) steering, which is a type of quantum correlation existing in the states without a local-hidden-state model, is observed in the two copy subsystems. This contradicts the conclusion of no-cloning of quantum steering(EPR steering) [C. Y. Chiu et al.,npj Quantum Inf. 2, 16020(2016)] based on a mutual information criterion for EPR steering.展开更多
A scheme for implementing nonlocal quantum cloning via quantum dots trapped in cavities is proposed.By modulating the parameters of the system,the optimal 1 → 2 universal quantum cloning machine,1 → 2 phase-covarian...A scheme for implementing nonlocal quantum cloning via quantum dots trapped in cavities is proposed.By modulating the parameters of the system,the optimal 1 → 2 universal quantum cloning machine,1 → 2 phase-covariant cloning machine,and 1 → 3 economical phase-covariant cloning machine are constructed.The present scheme,which is attainable with current technology,saves two qubits compared with previous cloning machines.展开更多
Probabilistic quantum cloning（PQC） cannot copy a set of linearly dependent quantum states.In this paper,we show that if incorrect copies are allowed to be produced,linearly dependent quantum states may also be clone...Probabilistic quantum cloning（PQC） cannot copy a set of linearly dependent quantum states.In this paper,we show that if incorrect copies are allowed to be produced,linearly dependent quantum states may also be cloned by the PQC.By exploiting this kind of PQC to clone a special set of three linearly dependent quantum states,we derive the upper bound of the maximum confidence measure of a set.An explicit transformation of the maximum confidence measure is presented.展开更多
We propose a method to improve the secret key rate of an eight-state continuous-variable quantum key distribution（CVQKD） by using a linear optics cloning machine（LOCM）. In the proposed scheme, an LOCM is exploited...We propose a method to improve the secret key rate of an eight-state continuous-variable quantum key distribution（CVQKD） by using a linear optics cloning machine（LOCM）. In the proposed scheme, an LOCM is exploited to compensate for the imperfections of Bob＇s apparatus, so that the generated secret key rate of the eight-state protocol could be well enhanced. We investigate the security of our proposed protocol in a finite-size scenario so as to further approach the practical value of a secret key rate. Numeric simulation shows that the LOCM with reasonable tuning gain λ and transmittance τcan effectively improve the secret key rate of eight-state CVQKD in both an asymptotic limit and a finite-size regime.Furthermore, we obtain the tightest bound of the secure distance by taking the finite-size effect into account, which is more practical than that obtained in the asymptotic limit.展开更多
By means of cavity-assisted photon interference, a simple scheme is proposed to implement a symmetric economical phase-covariant quantum cloning machine of two remote qubits, with each in a separate cavity. With our p...By means of cavity-assisted photon interference, a simple scheme is proposed to implement a symmetric economical phase-covariant quantum cloning machine of two remote qubits, with each in a separate cavity. With our present scheme, a high-fidelity cloning machine is realized. Our scheme may be quite useful in terms of distributed quantum information processing.展开更多
Background:Tumor cell heterogeneity mediated drug resistance has been recognized as the stumbling block of cancer treatment.Elucidating the cytotoxicity of anticancer drugs at single-cell level in a high-throughput wa...Background:Tumor cell heterogeneity mediated drug resistance has been recognized as the stumbling block of cancer treatment.Elucidating the cytotoxicity of anticancer drugs at single-cell level in a high-throughput way is thus of great value for developing precision therapy.However,current techniques suffer from limitations in dynamically characterizing the responses of thousands of single cells or cell clones presented to multiple drug conditions.Methods:We developed a new microfluidics-based“SMART”platform that is Simple to operate,able to generate a Massive single-cell array and Multiplex drug concentrations,capable of keeping cells Alive,Retainable and Trackable in the microchambers.These features are achieved by integrating a Microfluidic chamber Array(4320 units)and a sixConcentration gradient generator(MAC),which enables highly efficient analysis of leukemia drug effects on single cells and cell clones in a high-throughput way.Results:A simple procedure produces 6 on-chip drug gradients to treat more than 3000 single cells or single-cell derived clones and thus allows an efficient and precise analysis of cell heterogeneity.The statistic results reveal that Imatinib(Ima)and Resveratrol(Res)combination treatment on single cells or clones is much more efficient than Ima or Res single drug treatment,indicated by the markedly reduced half maximal inhibitory concentration(IC50).Additionally,single-cell derived clones demonstrate a higher IC_(50) in each drug treatment compared to single cells.Moreover,primary cells isolated from two leukemia patients are also found with apparent heterogeneity upon drug treatment on MAC.Conclusions:This microfluidics-based“SMART”platform allows high-throughput single-cell capture and culture,dynamic drug-gradient treatment and cell response monitoring,which represents a new approach to efficiently investigate anticancer drug effects and should benefit drug discovery for leukemia and other cancers.展开更多
We show that the secret key generation rate can be balanced with the maximum secure distance of four-state continuous-variable quantum key distribution（CV-QKD） by using the linear optics cloning machine（LOCM）. Ben...We show that the secret key generation rate can be balanced with the maximum secure distance of four-state continuous-variable quantum key distribution（CV-QKD） by using the linear optics cloning machine（LOCM）. Benefiting from the LOCM operation, the LOCM-tuned noise can be employed by the reference partner of reconciliation to achieve higher secret key generation rates over a long distance. Simulation results show that the LOCM operation can flexibly regulate the secret key generation rate and the maximum secure distance and improve the performance of four-state CV-QKD protocol by dynamically tuning parameters in an appropriate range.展开更多
The critical antioxidant catalase(CAT)breaks down hydrogen peroxide induced by environmental stresses.Here we cloned full length catalase cDNA from Lymantria dispar asiatic(LdCAT).Bioinformatic analyses showed that op...The critical antioxidant catalase(CAT)breaks down hydrogen peroxide induced by environmental stresses.Here we cloned full length catalase cDNA from Lymantria dispar asiatic(LdCAT).Bioinformatic analyses showed that open reading frames of LdCAT contains 1524 bp,encoding 507 amino acids with molecular weight of 126.99 kDa,theoretical pI of 5.00,aliphatic index of 29.92,grand average of hydropathicity of 0.764,and instability index(II)of 46.56.Protein BLAST and multiple sequence alignment indicated that LdCAT had high identity with CAT from other insects,especially lepidopterans.In a phylogenetic analysis,LdCAT was most similar to CAT from Spodoptera litura and S.exigua.Quantitative realtime polymerase chain reaction showed that LdCAT transcripts in all instar larvae and the five tissues tested,verifying the ubiquity of LdCAT in L.disapr.Moreover,LdCAT of third instar larvae was significantly upregulated after they fed on avermectin at sublethal and LC10 doses.The highest relative transcript levels were found 2 h after an avermectin spray at LC90,and in the cuticula,rather than heads,fat bodies,malpighian tubes,and midguts after a spray avermectin at a sublethal concentration.The expression level of LdCAT under pesticide stresses here suggested that CAT is an important antioxidant enzyme of L.disapr defensing against pesticide stress and may be a good target for controlling this pest.展开更多
Studies on the cold-responsive genes and cold signaling of woody species drop far behind in comparison to herbaceous plants.Due to similar lignified structure,perennial characteristic,and enhanced tolerance,it seems m...Studies on the cold-responsive genes and cold signaling of woody species drop far behind in comparison to herbaceous plants.Due to similar lignified structure,perennial characteristic,and enhanced tolerance,it seems much easier to find strongly antifreeze genes and obtain effective results in transgenic woody plants.In this study,Ammopiptanthus mongolicus,an evergreen,broadleaf and cold-resist leguminous shrub growing in the desert of Inner Mongolia,was used as a material for low-temperature induced gene isolation.Through differential expression analysis induced by low-temperature,thirteen up-regulated cDNAs were identified.One of them,AmEBP1,(accession number:DQ519359)confers enhanced cold-tolerance to both transgenic E.coli and transgenic Arabidopsis.Results suggest that AmEBP1 can stimulate the synthesis of ribosome and the dephosphyration of the α-subunit of initiation factor 2(eIF2α),and subsequently promote the translation process.By which the transgenic plants obtained increased cold-resistant ability.展开更多
RELATED TO AP2.12(RAP2.12)is one of the Ethylene Response Factors(ERF)transcription factor and plays a key role in controlling plant root bending and responding to multiple abiotic stresses including hypoxia stress.In...RELATED TO AP2.12(RAP2.12)is one of the Ethylene Response Factors(ERF)transcription factor and plays a key role in controlling plant root bending and responding to multiple abiotic stresses including hypoxia stress.In this study,FmRAP2.12 gene was isolated and characterized from Fraxinus mandshurica Rupr.The open reading frame(ORF)of FmRAP2.12 was 1170 bp and encoded a protein of 389 amino acids.The conserved domains,three-dimensional phylogenetic relationship of FmRAP2.12 was also investigated.Quantitative real-time(qRT-PCR)analyzed the expression of FmRAP2.12 in different tissues.The expression level of FmRAP2.12 was highest in roots followed by leaves,and lowest in male flowers.Abiotic stress and hormone signal-induced expression was established using qRT-PCR.Salt stress induced FmRAP2.12 to a double peak pattern:the first peak value was at 6 h and the second at 72 h.Drought stress also induced FmRAP2.12 to a double peak pattern:the first at6 h and the second at 48 h.FmRAP2.12 was up-regulated after initiation of gibberellic acid(GA3)treatment,with a one peak pattern at 24 h.FmRAP2.12 may not respond to cold stress and Abscisic acid(ABA)treatment.The transient overexpression of FmRAP2.12 caused the up-expression of downstream key genes of abiotic stress response and gibberellin pathway.Our research reveals the molecular characteristic and expression patterns under abiotic stress and hormone condition of FmRAP2.12,providing support for the genetic improvement of F.mandshurica at a molecular level.展开更多
One oligonueleotide probe,HIV env 101-1,and two oligonucleotide primers,HIV env125-1 and HIV env 125-2,were designed with the aid of a computer and synthesized by a DNAsynthesizer.The env 125 peptide gene was amplifie...One oligonueleotide probe,HIV env 101-1,and two oligonucleotide primers,HIV env125-1 and HIV env 125-2,were designed with the aid of a computer and synthesized by a DNAsynthesizer.The env 125 peptide gene was amplified by polymerase chain reaetion(PCR).Beingidentified by electrophoresis and Southern blotting,the PCR product was cloned into plasmidpUC 19.The recombinant pENV 125,identified with X-gal selection and restriction mapping, wassequenced.The results showed that the cloned env 125 peptide gene contained the inserted EcoRⅠ site and ATG at the 5’end,Hind Ⅲ site and TAG at the 3’end.The sequence and readingframe were proved to be correct.展开更多
Plant nonspecific lipid transfer proteins (nsLTPs) are widely distributed through plant kingdom and are characterized by the presence of a central hydrophobic cavity, suitable for binding various hydrophobic molecules...Plant nonspecific lipid transfer proteins (nsLTPs) are widely distributed through plant kingdom and are characterized by the presence of a central hydrophobic cavity, suitable for binding various hydrophobic molecules. Despite extensive research on nsLTP in different plant species, mostly angiosperm, and the great diversity of physiological processes in which they seem to be involved, their exact functions still remain unclear. Also, very limited experimental data are available on nsLTP in gymnosperm. In this study, we report for the first time on the molecular cloning of nsLTP, from Pinus sylvestris L.(PsLTP1, GenBank accession JN980402.1) and the expression pattern of PsLTP1 during ontogenesis and in response to environmental stress conditions. Total RNA from roots of 7-day old pine seedlings was used to isolate the cDNA clone, corresponding to Scots pine lipid transfer protein. The open reading frame of PsLTP1 consists of 372 bp encoding a protein of 123 amino acids. Amino acid sequence alignment revealed that mature PsLTP1 shares high level of similarity with nsLTP from other conifers and with well-studied nsLTPs from angiosperms. The PsLTP1 contains a 27-amino-acid N-terminal signal sequence and presents all the features of a plant nsLTP. Amino acid comparison analysis and 3D structure prediction showed that PsLTP1 is a type 1 nsLTP. The results of the expression analysis of Scots pine PsLTP1 gene revealed that its transcripts accumulate in actively growing tissues. Furthermore, transcription of PsLTP1 was upregulated in response to cold and salt treatments, and downregulated during acidic, osmotic and water stresses.展开更多
基金supported by the National Natural Science Foundation of China (Grant No 10674001)the Program of the Education Department of Anhui Province of China (Grant No KJ2007A002)
文摘This paper presents a very simple method to derive the explicit transformations of the optimal economical 1 to M phase-covariant cloning. The fidelity of clones reaches the theoretic bound [D＇Ar]ano G M and Macchiavello C 2003 Phys. Rev. A 67 042306]. The derived transformations cover the previous contributions [Delgado Y, Lamata Let al, 2007 Phys. Rev. Lett. 98 150502] in which M must be odd.
基金supported by the National Natural Science Foundation of China(Grant Nos.11074002,61073048,and 11104057)the Natural Science Foundationof the Education Department of Anhui Province,China(Grant Nos.KJ2010ZD08 and KJ2012A245)the Postgraduate Program of Huainan NormalUniversity of China
文摘In this paper, we derive the explicit transformations of the optimal 1→3, 4, 5 phase-covariant cloning in three dimensions, and then generalize them to the cases of 1 → M = 3n, 3n ＋ 1, 3n ＋ 2 （n ≥ 1 integer） cloning. The clone fidelities are coincident with the theoretical bounds found.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.11074002,61275119,and 11247009)the Doctoral Foundation of the Ministry of Education of China(Grant No.20103401110003)
文摘We review the basic theory of approximate quantum cloning for discrete variables and some schemes for implementing quantum cloning machines. Several types of approximate quantum clones and their expansive quantum clones are intro- duced. As for the implementation of quantum cloning machines, we review some design methods and recent experimental results.
文摘This paper proposes a scheme where one can realize quantum cloning of an unknown two-atom entangled state with assistance of a state preparer in cavity QED. The first stage of the scheme requires usual teleportation. In the second stage of the scheme, with the assistance of the preparer, the perfect copies of an unknown atomic entangled state can be produced.
基金Project supported by the National Natural Science Foundation of China(Grant Nos10574022 and 10575022)the Funds of the Natural Science of Fujian Province,China(Grant Nos Z0512006 and A0210014)
文摘This paper proposes a scheme for the implementation of 1→ 3 optimal phase-covariant quantum cloning with trapped ions. In the present protocol, the required time for the whole procedure is short due to the resonant interaction, which is important in view of decoherence. Furthermore, the scheme is feasible based on current technologies.
文摘Two quantum logic networks are proposed to simulate a cloning machine that copies the states near a given one. Probabilistie cloning based on the first network is realized and the cloning probability of success based on the second network is lOOe/0. Therefore, the second network is more motivative than the first one.
基金supported by the National Natural Science Foundation of China (Grant No 10674001)also by the Program of the Education Department of Anhui Province (Grant No KJ2007A002)
文摘This paper presents a quantum network to implement the optimal 1→2 quantum cloning in 2 dimensions, including the optimal asymmetric universal, the optimal symmetric phase-covariant, and the asymmetric real state cloning. By only choosing different angles of the single-qubit rotations, the quantum network can implement three optimal quantum cloning.
基金supported by the National Natural Science Foundation of China (Grant Nos. 11675119, 11575125, and 11105097)。
文摘Quantum steering in a global state allows an observer to remotely steer a subsystem into different ensembles by performing different local measurements on the other part. We show that, in general, this property cannot be perfectly cloned by any joint operation between a steered subsystem and a third system. Perfect cloning is viable if and only if the initial state is of zero discord. We also investigate the process of cloning the steered qubit of a Bell state using a universal cloning machine. Einstein–Podolsky–Rosen(EPR) steering, which is a type of quantum correlation existing in the states without a local-hidden-state model, is observed in the two copy subsystems. This contradicts the conclusion of no-cloning of quantum steering(EPR steering) [C. Y. Chiu et al.,npj Quantum Inf. 2, 16020(2016)] based on a mutual information criterion for EPR steering.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. 61068001 and 11165015)the Nature Science Foundation of Jilin Province,China (Grant No. 201115226)
文摘A scheme for implementing nonlocal quantum cloning via quantum dots trapped in cavities is proposed.By modulating the parameters of the system,the optimal 1 → 2 universal quantum cloning machine,1 → 2 phase-covariant cloning machine,and 1 → 3 economical phase-covariant cloning machine are constructed.The present scheme,which is attainable with current technology,saves two qubits compared with previous cloning machines.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. 11074002,61073048,and 11104057)the Natural Science Foundation of the Education Department of Anhui Province,China (Grant Nos. KJ2010ZD08 and KJ2012A245)the Postgraduate Program of Huainan Normal University of China
文摘Probabilistic quantum cloning（PQC） cannot copy a set of linearly dependent quantum states.In this paper,we show that if incorrect copies are allowed to be produced,linearly dependent quantum states may also be cloned by the PQC.By exploiting this kind of PQC to clone a special set of three linearly dependent quantum states,we derive the upper bound of the maximum confidence measure of a set.An explicit transformation of the maximum confidence measure is presented.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.61379153 and 61572529)
文摘We propose a method to improve the secret key rate of an eight-state continuous-variable quantum key distribution（CVQKD） by using a linear optics cloning machine（LOCM）. In the proposed scheme, an LOCM is exploited to compensate for the imperfections of Bob＇s apparatus, so that the generated secret key rate of the eight-state protocol could be well enhanced. We investigate the security of our proposed protocol in a finite-size scenario so as to further approach the practical value of a secret key rate. Numeric simulation shows that the LOCM with reasonable tuning gain λ and transmittance τcan effectively improve the secret key rate of eight-state CVQKD in both an asymptotic limit and a finite-size regime.Furthermore, we obtain the tightest bound of the secure distance by taking the finite-size effect into account, which is more practical than that obtained in the asymptotic limit.
文摘By means of cavity-assisted photon interference, a simple scheme is proposed to implement a symmetric economical phase-covariant quantum cloning machine of two remote qubits, with each in a separate cavity. With our present scheme, a high-fidelity cloning machine is realized. Our scheme may be quite useful in terms of distributed quantum information processing.
基金funded by the National Natural Science Foundation of China(21904139)。
文摘Background:Tumor cell heterogeneity mediated drug resistance has been recognized as the stumbling block of cancer treatment.Elucidating the cytotoxicity of anticancer drugs at single-cell level in a high-throughput way is thus of great value for developing precision therapy.However,current techniques suffer from limitations in dynamically characterizing the responses of thousands of single cells or cell clones presented to multiple drug conditions.Methods:We developed a new microfluidics-based“SMART”platform that is Simple to operate,able to generate a Massive single-cell array and Multiplex drug concentrations,capable of keeping cells Alive,Retainable and Trackable in the microchambers.These features are achieved by integrating a Microfluidic chamber Array(4320 units)and a sixConcentration gradient generator(MAC),which enables highly efficient analysis of leukemia drug effects on single cells and cell clones in a high-throughput way.Results:A simple procedure produces 6 on-chip drug gradients to treat more than 3000 single cells or single-cell derived clones and thus allows an efficient and precise analysis of cell heterogeneity.The statistic results reveal that Imatinib(Ima)and Resveratrol(Res)combination treatment on single cells or clones is much more efficient than Ima or Res single drug treatment,indicated by the markedly reduced half maximal inhibitory concentration(IC50).Additionally,single-cell derived clones demonstrate a higher IC_(50) in each drug treatment compared to single cells.Moreover,primary cells isolated from two leukemia patients are also found with apparent heterogeneity upon drug treatment on MAC.Conclusions:This microfluidics-based“SMART”platform allows high-throughput single-cell capture and culture,dynamic drug-gradient treatment and cell response monitoring,which represents a new approach to efficiently investigate anticancer drug effects and should benefit drug discovery for leukemia and other cancers.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.61379153 and 61572529)
文摘We show that the secret key generation rate can be balanced with the maximum secure distance of four-state continuous-variable quantum key distribution（CV-QKD） by using the linear optics cloning machine（LOCM）. Benefiting from the LOCM operation, the LOCM-tuned noise can be employed by the reference partner of reconciliation to achieve higher secret key generation rates over a long distance. Simulation results show that the LOCM operation can flexibly regulate the secret key generation rate and the maximum secure distance and improve the performance of four-state CV-QKD protocol by dynamically tuning parameters in an appropriate range.
文摘The critical antioxidant catalase(CAT)breaks down hydrogen peroxide induced by environmental stresses.Here we cloned full length catalase cDNA from Lymantria dispar asiatic(LdCAT).Bioinformatic analyses showed that open reading frames of LdCAT contains 1524 bp,encoding 507 amino acids with molecular weight of 126.99 kDa,theoretical pI of 5.00,aliphatic index of 29.92,grand average of hydropathicity of 0.764,and instability index(II)of 46.56.Protein BLAST and multiple sequence alignment indicated that LdCAT had high identity with CAT from other insects,especially lepidopterans.In a phylogenetic analysis,LdCAT was most similar to CAT from Spodoptera litura and S.exigua.Quantitative realtime polymerase chain reaction showed that LdCAT transcripts in all instar larvae and the five tissues tested,verifying the ubiquity of LdCAT in L.disapr.Moreover,LdCAT of third instar larvae was significantly upregulated after they fed on avermectin at sublethal and LC10 doses.The highest relative transcript levels were found 2 h after an avermectin spray at LC90,and in the cuticula,rather than heads,fat bodies,malpighian tubes,and midguts after a spray avermectin at a sublethal concentration.The expression level of LdCAT under pesticide stresses here suggested that CAT is an important antioxidant enzyme of L.disapr defensing against pesticide stress and may be a good target for controlling this pest.
文摘Studies on the cold-responsive genes and cold signaling of woody species drop far behind in comparison to herbaceous plants.Due to similar lignified structure,perennial characteristic,and enhanced tolerance,it seems much easier to find strongly antifreeze genes and obtain effective results in transgenic woody plants.In this study,Ammopiptanthus mongolicus,an evergreen,broadleaf and cold-resist leguminous shrub growing in the desert of Inner Mongolia,was used as a material for low-temperature induced gene isolation.Through differential expression analysis induced by low-temperature,thirteen up-regulated cDNAs were identified.One of them,AmEBP1,(accession number:DQ519359)confers enhanced cold-tolerance to both transgenic E.coli and transgenic Arabidopsis.Results suggest that AmEBP1 can stimulate the synthesis of ribosome and the dephosphyration of the α-subunit of initiation factor 2(eIF2α),and subsequently promote the translation process.By which the transgenic plants obtained increased cold-resistant ability.
基金supported by the National Key Research and Development Project of China(No.2017YFD0600605-01)the National Natural Science Foundation of China(NSFC)(No.31270697)
文摘RELATED TO AP2.12(RAP2.12)is one of the Ethylene Response Factors(ERF)transcription factor and plays a key role in controlling plant root bending and responding to multiple abiotic stresses including hypoxia stress.In this study,FmRAP2.12 gene was isolated and characterized from Fraxinus mandshurica Rupr.The open reading frame(ORF)of FmRAP2.12 was 1170 bp and encoded a protein of 389 amino acids.The conserved domains,three-dimensional phylogenetic relationship of FmRAP2.12 was also investigated.Quantitative real-time(qRT-PCR)analyzed the expression of FmRAP2.12 in different tissues.The expression level of FmRAP2.12 was highest in roots followed by leaves,and lowest in male flowers.Abiotic stress and hormone signal-induced expression was established using qRT-PCR.Salt stress induced FmRAP2.12 to a double peak pattern:the first peak value was at 6 h and the second at 72 h.Drought stress also induced FmRAP2.12 to a double peak pattern:the first at6 h and the second at 48 h.FmRAP2.12 was up-regulated after initiation of gibberellic acid(GA3)treatment,with a one peak pattern at 24 h.FmRAP2.12 may not respond to cold stress and Abscisic acid(ABA)treatment.The transient overexpression of FmRAP2.12 caused the up-expression of downstream key genes of abiotic stress response and gibberellin pathway.Our research reveals the molecular characteristic and expression patterns under abiotic stress and hormone condition of FmRAP2.12,providing support for the genetic improvement of F.mandshurica at a molecular level.
文摘One oligonueleotide probe,HIV env 101-1,and two oligonucleotide primers,HIV env125-1 and HIV env 125-2,were designed with the aid of a computer and synthesized by a DNAsynthesizer.The env 125 peptide gene was amplified by polymerase chain reaetion(PCR).Beingidentified by electrophoresis and Southern blotting,the PCR product was cloned into plasmidpUC 19.The recombinant pENV 125,identified with X-gal selection and restriction mapping, wassequenced.The results showed that the cloned env 125 peptide gene contained the inserted EcoRⅠ site and ATG at the 5’end,Hind Ⅲ site and TAG at the 3’end.The sequence and readingframe were proved to be correct.
基金supported by grants from the Ministry of Education and Science of Ukraine(0116U003593)grant from cieA3(Campus de Excelencia Internacional Agroalimentario)-UCO,Spain
文摘Plant nonspecific lipid transfer proteins (nsLTPs) are widely distributed through plant kingdom and are characterized by the presence of a central hydrophobic cavity, suitable for binding various hydrophobic molecules. Despite extensive research on nsLTP in different plant species, mostly angiosperm, and the great diversity of physiological processes in which they seem to be involved, their exact functions still remain unclear. Also, very limited experimental data are available on nsLTP in gymnosperm. In this study, we report for the first time on the molecular cloning of nsLTP, from Pinus sylvestris L.(PsLTP1, GenBank accession JN980402.1) and the expression pattern of PsLTP1 during ontogenesis and in response to environmental stress conditions. Total RNA from roots of 7-day old pine seedlings was used to isolate the cDNA clone, corresponding to Scots pine lipid transfer protein. The open reading frame of PsLTP1 consists of 372 bp encoding a protein of 123 amino acids. Amino acid sequence alignment revealed that mature PsLTP1 shares high level of similarity with nsLTP from other conifers and with well-studied nsLTPs from angiosperms. The PsLTP1 contains a 27-amino-acid N-terminal signal sequence and presents all the features of a plant nsLTP. Amino acid comparison analysis and 3D structure prediction showed that PsLTP1 is a type 1 nsLTP. The results of the expression analysis of Scots pine PsLTP1 gene revealed that its transcripts accumulate in actively growing tissues. Furthermore, transcription of PsLTP1 was upregulated in response to cold and salt treatments, and downregulated during acidic, osmotic and water stresses.
