Lei Wang

Shanghai Research Institute of Chemical Industry, Shanghai, Shanghai Shi, China

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Publications (227)527.67 Total impact

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    ABSTRACT: We isolated a novel defence gene (AsDef) cDNAs from Actias selene (Hübner 1806) (Lepidoptera: Saturniidae). It contained 691 nucleotides with a putative open reading frame of 498 bp encoding 165 amino acid residues with a reeler domain. It showed significant similarities with defence proteins from several other lepidopteran insect species including Samia ricini (Donovan 1798), Antheraea mylitta (Drury 1773), Bombyx mori (Linnaeus 1758), Lonomia oblique (Walker 1855), Hyphantria cunea (Drury 1773) and Manduca sexta (Linnaeus 1763). The recombinant protein of AsDef was expressed successfully in Escherichia coli (Migula 1895) cells, and the anti-AsDef antibody against rabbit was prepared. Results of real-time quantitative Polymerase Chain Reaction (PCR) and western blot showed that AsDef gene was detected at a particularly high levels in fat body, while AsDef protein can only be detected in haemolymph. For immune functions, AsDef gene can be upregulated by E. coli, Micrococcus luteus (Cohn 1872), Beauveria bassiana (Bals 1912) and nuclear polyhedrosis virus, and showed a stronger sensitivity for Gram-positive bacteria than fungi and virus, while the least sensitivity for Gram-negative bacteria. These data indicated that AsDef played an important role in innate immune responses of A. selene.
    Oriental insects 11/2015; DOI:10.1080/00305316.2015.1081648 · 0.27 Impact Factor
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    ABSTRACT: Perovskite bismuth ferrite-BFO (111) membranes, as a potential sensitive electrochemical sensor, are investigated for the detection of amino acids by molecular dynamics (MD) and density functional theory (DFT) techniques. For the detection mechanism of the ferromagnetic phase BFO (111) membrane, the cation bridge model indicates that there is a electronic signal amplification (0.01–0.09 V), due to the enhancement of Fe3+–COO− triple degeneracy orbit (t2g). It is an excellent detection sensitivity for various AAs that can be used to distinguish the surface charges. However, the Fe-d7/2 momentum changes its orientation from upward to downward, on the anti-ferromagnetic phase BFO (111) membrane. The empty d0 orbital degenerates to the O↓ orbital that weakens the Fe–O electron transfer rate, weakening the electronic signal (0.005–0.05 V).
  • Lei Wang · Lianrui Hu · Hezhong Zhang · Hui Chen · Liang Deng ·
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    ABSTRACT: High-valent iron imido species are implicated as reactive intermediates in many iron-catalyzed transformations. However, isolable complexes of this type are rare, and their reactivity is poorly understood. Herein, we report the synthesis, characterization, and reactivity studies on novel three-coordinate iron(IV) bisimido complexes with aminocarbene ligation. Using our recently reported synthetic method for [LFe(NDipp)2] (L = IMes, 1; Me2-cAAC, 2), four new iron(IV) imido complexes, [(IPr)Fe(NDipp)2] (3) and [(Me2-cAAC)Fe(NR)2] (R = Mes, 4; Ad, 5; CMe2CH2Ph, 6), were prepared from the reactions of three-coordinate iron(0) compounds with organic azides. Characterization data acquired from (1)H and (13)C NMR spectroscopy, (57)Fe Mössbauer spectroscopy, and X-ray diffraction studies suggest a low-spin singlet ground state for these iron(IV) complexes and the multiple-bond character of their Fe-N bonds. A reactivity study taking the reactions of 1 as representative revealed an intramolecular alkane dehydrogenation of 1 to produce the iron(II) complex [(IMes)Fe(NHDipp)(NHC6H3-2-Pr(i)-6-CMe═CH2)] (7), a Si-H bond activation reaction of 1 with PhSiH3 to produce the iron(II) complex [(IMes)Fe(NHDipp)(NDippSiPhH2)] (8), and a [2+2]-addition reaction of 1 with PhNCNPh and p-Pr(i)C6H4NCO to form the corresponding open-shell formal iron(IV) monoimido complexes [(IMes)Fe(NDipp)(N(Dipp)C(NPh)(═NPh))] (9) and [(IMes)Fe(NDipp)(N(Dipp)C(O)N(p-Pr(i)C6H4))] (10), as well as [NDipp]-group-transfer reactions with CO and Bu(t)NC. Density functional theory calculations suggested that the alkane chain dehydrogenation reaction starts with a hydrogen atom abstraction mechanism, whereas the Si-H activation reaction proceeds in a [2π+2σ]-addition manner. Both reactions have the pathways at the triplet potential energy surfaces being energetically preferred, and have formal iron(IV) hydride and iron(IV) silyl species as intermediates, respectively. The low-coordinate nature and low d-electron count (d(4)) of iron(IV) imido complexes are thought to be the key features endowing their unique reactivity.
    Journal of the American Chemical Society 10/2015; 137(44). DOI:10.1021/jacs.5b09579 · 12.11 Impact Factor
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    ABSTRACT: Dietary supplementation with N-acetylcysteine (NAC) has been reported to improve intestinal health and treat gastrointestinal diseases. However, the underlying mechanisms are not fully understood. According to previous reports, NAC was thought to exert its effect through glutathione synthesis. This study tested the hypothesis that NAC enhances enterocyte growth and protein synthesis independently of cellular glutathione synthesis. Intestinal porcine epithelial cells were cultured for 3 days in Dulbecco's modified Eagle medium containing 0 or 100 μM NAC. To determine a possible role for GSH (the reduced form of glutathione) in mediating the effect of NAC on cell growth and protein synthesis, additional experiments were conducted using culture medium containing 100 μM GSH, 100 μM GSH ethyl ester (GSHee), diethylmaleate (a GSH-depletion agent; 10 μM), or a GSH-synthesis inhibitor (buthionine sulfoximine, BSO; 20 μM). NAC increased cell proliferation, GSH concentration, and protein synthesis, while inhibiting proteolysis. GSHee enhanced cell proliferation and GSH concentration without affecting protein synthesis but inhibited proteolysis. Conversely, BSO or diethylmaleate reduced cell proliferation and GSH concentration without affecting protein synthesis, while promoting protein degradation. At the signaling level, NAC augmented the protein abundance of total mTOR, phosphorylated mTOR, and phosphorylated 70S6 kinase as well as mRNA levels for mTOR and p70S6 kinase in IPEC-1 cells. Collectively, these results indicate that NAC upregulates expression of mTOR signaling proteins to stimulate protein synthesis in enterocytes independently of GSH generation. Our findings provide a hitherto unrecognized biochemical mechanism for beneficial effects of NAC in intestinal cells.
    Amino Acids 10/2015; DOI:10.1007/s00726-015-2105-z · 3.29 Impact Factor
  • Yan Wang · Lei Wang · Yulan Liu · Pei Ding · Shiming Deng · Enshen Long ·

    Urban Climate 10/2015; DOI:10.1016/j.uclim.2015.09.008 · 0.36 Impact Factor
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    ABSTRACT: Three Keggin-type heteropoly catalysts with different vanadyl species, H4PMo11VO40 (V existing in the primary structure), HVOPMo12O40 (V existing as VO2+ in the secondary structure), and V2O5/H3PMo12O40 (V existing in V2O5 before calcination), were prepared and studied to identify the preferable vanadyl species for oxidation of methacrolein to methacrylic acid. The catalysts were characterized by FT-IR, Raman, XRD, UV–vis, EPR, and XPS before and after calcination at different temperatures. The calcined catalysts were applied in the selective oxidation of methacrolein. The chemical state and position of the vanadyl species varied with the treatment temperature. Compared with the VO2+ species in HVOPMo12O40, the VO2+ species generated in H4PMo11VO40 and V2O5/H3PMo12O40 during calcination processes showed very different promotional effects, and the VO2+ species that interact with the Keggin structure turned to be the main active vanadyl species in all the catalysts. The active vanadyl species changed from an independent ion form to a squashed square pyramidal on Keggin structure or defect Keggin structure during the oxidation reaction. The optimum conversion of methacrolein and selectivity to methacrylic acid were obtained on the V2O5/H3PMo12O40 catalyst calcined at 350 °C, so a new means of adding vanadium in the Keggin-type heteropoly catalysts to obtain high selectivity to methacrylic acid is proposed.
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    ABSTRACT: In this study, we investigated the role of karyopherin alpha 3 in the heat shock response in male silkworm pupae. Karyopherin alpha recognizes the classical nuclear location sequence on proteins and transports them into the nucleus by forming a trimetric complex with karyopherin beta. Three predicted karyopherin alphas (KPNA1, KPNA2 and KPNA3) have been identified from the silkworm Bombyx mori. Pull-down assay result showed that KPNA3 can pull down heat shock transcription factor (HSF) from proteins extracted from tissues using non-denature lysis buffer. After 45°C heat shock on male B. mori pupae for 30 min, we identified two heat shock protein (HSP) mRNA expression peaks correlating with HSP19.9, HSP20.4 and HSP25.4 at 4 h (peak 1) and 24 h (peak 2). The second peak was eliminated after knockdown of KPNA3. Similar results were obtained following knockdown of HSF, which is the trans-activating factor of heat shock. However, KPNA3 knockdown was not accompanied by the decreased HSF protein levels at 24 h after heat shock which were observed following HSF knockdown. We also expressed recombinant protein GST-KPNA3 and His-HSF in Escherichia coli to perform GST pull-down assay and the result confirmed the interaction between KPNA3 and HSF. We concluded that KPNA3 knockdown eliminates the second heat shock protein peak in the heat shock response of male silkworm pupae by reducing HSF transport into the nucleus.
    Gene 09/2015; 575(2P2). DOI:10.1016/j.gene.2015.09.018 · 2.14 Impact Factor
  • Cen Qian · Qi Fang · Lei Wang · Gong-Yin Ye ·

    Toxins 09/2015; 7(9):3636-3636. DOI:10.3390/toxins7093636 · 2.94 Impact Factor
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    ABSTRACT: This study was carried out to investigate the effects of tributyrin (TB) on the growth performance, pro-inflammatory cytokines, intestinal morphology, energy status, disaccharidase activity, and antioxidative capacity of broilers challenged with lipopolysaccharide (LPS). A total of 160 one-day-old Cobb broilers were allocated to 1 of 4 treatments, with 4 replicated pens per treatment and 10 birds per pen. The experiment consisted of a 2×2 factorial arrangements of treatments with TB supplementation (0 or 500 mg/kg) and LPS challenge (0 or 500 μg/kg body weight [BW]). On days 22, 24, and 26 of the trial, broilers received an intraperitoneal administration of 500 μg/kg BW LPS or saline. Dietary TB showed no effect on growth performance. However, LPS challenge decreased the average daily gain of broilers from day 22 to day 26 of the trial. Dietary TB supplementation inhibited the increase of interleukin-1β (in the jejunum and ileum), interleukin-6 (in the duodenum and jejunum), and prostaglandin E2 (in the duodenum) of LPS-challenged broilers. Similar inhibitory effects of TB in the activities of total nitric oxide synthase (in the ileum) and inducible nitric oxide synthase (in the jejunum) were also observed in birds challenged with LPS. Additionally, TB supplementation mitigated the decrease of ileal adenosine triphosphate, adenosine diphosphate and total adenine nucleotide and the reduction of jejunal catalase activity induced by LPS. Taken together, these results suggest that the TB supplementation was able to reduce the release of pro-inflammatory cytokines and improve the energy status and anti-oxidative capacity in the small intestine of LPS-challenged broilers.
    Asian Australasian Journal of Animal Sciences 09/2015; 28(12). DOI:10.5713/ajas.15.0286 · 0.54 Impact Factor
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    ABSTRACT: CH3NH3PbIxBr3-x thin films on FTO substrate were synthesized successfully. The crystal structure and optical properties of these films changed with different ratios of I-/Br- ions. The lattice parameters were reduced and the optical absorption edges were blue-shifted with the increasing ratio of Br- ions. The dielectric spectra have revealed that tetragonal CH3NH3PbIxBr3-x films at room temperature not only have a lower symmetry than cubic films, but also provide more electron transition energies. The mechanism is discussed correspondingly.
  • Yuesheng Liu · Lei Wang · Liang Deng ·
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    ABSTRACT: The reaction of [(IPr2Me2)2FePh2] with PhC≡CPh furnished a three-coordinate iron(II) dialkenyl complex, [(IPr2Me2)Fe(σ-CPh=CPh2)2] (1, IPr2Me2 = 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene), that represents a rare example of isolable low-coordinate iron alkenyl complexes with a high-spin ground state. Complex 1 was characterized by 1H NMR spectroscopy, solution magnetic susceptibility measurement, Mössbauer spectroscopy, single-crystal X-ray diffraction study, and elemental analyses. A reactivity study revealed the reactions of 1 with PhCH2Cl to produce cross-coupling product Ph2C=CPhCH2Ph (2), with [Cp2Fe][BArF4] to yield Ph2C=CPh-CPh=CPh2 (3), and with CO, 2,6-dimethylphenyl isocyanide, and phenyl azide to produce novel iron(0) and iron(II) complexes 4-6 bearing triphenylvinyl-derived ligands. These transformations demonstrated the high reactivity of the low-coordinate iron alkenyl complex.
    Organometallics 08/2015; 34(17):150827152819004. DOI:10.1021/acs.organomet.5b00632 · 4.13 Impact Factor
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    ABSTRACT: The complete mitochondrial genome (mitogenome) of Cerura menciana (Lepidoptera: Notodontidae) was sequenced and analyzed in this study. The mitogenome is a circular molecule of 15,369 bp, containing 13 protein-coding genes (PCGs), two ribosomal RNA (rRNA) genes, 22 transfer RNA (tRNA) genes and a A+T-rich region. The positive AT skew (0.031) indicated that more As than Ts were present. All PCGs were initiated by ATN codons, except for the cytochrome c oxidase subunit 1 (cox1) gene, which was initiated by CAG. Two of the 13 PCGs contained the incomplete termination codon T or TA, while the others were terminated with the stop codon TAA. The A+T-rich region was 372 bp in length and consisted of an 'ATAGA' motif followed by an 18 bp poly-T stretch, a microsatellite-like (AT)8 and a poly-A element upstream of the trnM gene. Results examining codon usage indicated that Asn, Ile, Leu2, Lys, Tyr and Phe were the six most frequently occurring amino acids, while Cys was the rarest. Phylogenetic relationships, analyzed based on the nucleotide sequences of the 13 PCGs from other insect mitogenomes, confirmed that C. menciana belongs to the Notodontidae family.
    PLoS ONE 08/2015; 10(8):e0132951. DOI:10.1371/journal.pone.0132951 · 3.23 Impact Factor
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    ABSTRACT: Several cyclized indole derivatives have been synthesized, and their structures been determined. The C3-symmetric single-chiral N-phenyltriindole (Tr-Ph3) crystallized in the P1 space group, and the S4-symmetric saddle-like tetraindole (TTr) crystallized in the I4̅ space group. The Tr-Ph3 and TTr crystals exhibit remarkable powder SHG intensities 5 and 11 times that of KH2PO4 (KDP), respectively. TTr is a useful octupolar core to build S4-symmetric molecules and crystals for second-NLO materials.
    Organic Letters 08/2015; 17(17):150825080049004. DOI:10.1021/acs.orglett.5b01912 · 6.36 Impact Factor
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    Chao Ma · Wei Ren · Lei Wang · Liang Bian · Jin Bao Xu · Ai Min Chang ·
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    ABSTRACT: The effects of cation distribution on optical properties of MnxCo2.52−xNi0.48O4 serial thin films are investigated by spectroscopic ellipsometry and Raman technique. The optical constants present a distinctive difference with the change of the cation distribution in the serial films. Three absorption structures are found in the dielectric constant spectra while their intensities strongly depend on the distribution of cations. Complementary Raman scattering measurements corroborate the varying absorptions are mainly contributed by Mn ions in high photon energy range but Co ions in low.
    Materials Letters 08/2015; 153. DOI:10.1016/j.matlet.2015.04.046 · 2.49 Impact Factor
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    ABSTRACT: The use of the N-heterocyclic carbene (NHC) ligands 1,3-bis(2',6'-diethylphenyl)-4,5-(CH2)4-imidazol-2-ylidene (cyIDep), 1,3-bis(2',6'-diethylphenyl)-imidazolin-2-ylidene (sIDep), and its N-mesityl analogue sIMes enables the preparation of the two-coordinate homoleptic iron(I)-NHC complexes [(cyIDep)2Fe][BAr(F)4] (3, Ar(F) denoted for 3,5-di(trifluoromethyl)phenyl) and [(sIDep)2Fe][BAr(F)4] (4) and the T-shaped iron(I)-NHC complex [(sIMes)2Fe(THF)][BPh4] (5, THF = tetrahydrofuran). Complexes 3-5 were prepared via the sequential protocol of control reduction of iron(II) dihalides by KC8 in the presence of the corresponding NHC ligands followed by halide-abstraction with NaBAr4. Spectroscopic characterization, including single-crystal X-ray diffraction studies and (57)Fe Mössbauer spectroscopy, in combination with density functional theory calculations, suggest their high-spin nature. Solution property study (absorption spectroscopy and cyclic voltammetry) indicates that 3 and 5 keep their corresponding two- and three-coordinate nature in THF solution, and 4 might reversibly coordinate a THF molecule to form, presumably, the T-shaped species [(sIDep)2Fe(THF)][BAr(F)4]. The isolation of 3 and 4 demonstrates the accessibility of homoleptic two-coordinate iron(I)-NHC complexes.
    Inorganic Chemistry 08/2015; 54(17). DOI:10.1021/acs.inorgchem.5b01522 · 4.76 Impact Factor
  • Cen Qian · Qi Fang · Lei Wang · Gong-Yin Ye ·
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    ABSTRACT: Two cDNA sequences of Kazal-type serine protease inhibitors (KSPIs) in Nasonia vitripennis, NvKSPI-1 and NvKSPI-2, were characterized and their open reading frames (ORFs) were 198 and 264 bp, respectively. Both NvKSPI-1 and NvKSPI-2 contained a typical Kazal-type domain. Real-time quantitative PCR (RT-qPCR) results revealed that NvKSPI-1 and NvKSPI-2 mRNAs were mostly detected specifically in the venom apparatus, while they were expressed at lower levels in the ovary and much lower levels in other tissues tested. In the venom apparatus, both NvKSPI-1 and NvKSPI-2 transcripts were highly expressed on the fourth day post eclosion and then declined gradually. The NvKSPI-1 and NvKSPI-2 genes were recombinantly expressed utilizing a pGEX-4T-2 vector, and the recombinant products fused with glutathione S-transferase were purified. Inhibition of recombinant GST-NvKSPI-1 and GST-NvKSPI-2 to three serine protease inhibitors (trypsin, chymotrypsin, and proteinase K) were tested and results showed that only NvKSPI-1 could inhibit the activity of trypsin. Meanwhile, we evaluated the influence of the recombinant GST-NvKSPI-1 and GST-NvKSPI-2 on the phenoloxidase (PO) activity and prophenoloxidase (PPO) activation of hemolymph from a host pupa, Musca domestica. Results showed PPO activation in host hemolymph was inhibited by both recombinant proteins; however, there was no significant inhibition on the PO activity. Our results suggested that NvKSPI-1 and NvKSPI-2 could inhibit PPO activation in host hemolymph and trypsin activity in vitro.
    Toxins 08/2015; 7(8):2888-2905. DOI:10.3390/toxins7082888 · 2.94 Impact Factor
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    ABSTRACT: The variations of work functions in Mn1.56Co0.96Ni0.48O4 (MCN) thin films are investigated in the temperature range from 30 to 80 [degree]C. The high resolution images of the contact potential difference (CPD) of MCN thin films were obtained through Kelvin probe force microscopy (KPFM) and the correlations between the work functions and temperatures were demonstrated through the imaginary part of the dielectric functions. The complex dielectric spectra are temperature dependent while their intensities have the inverse trend according to the work functions. The phenomenon can be interpreted by different chemical states that relate to the Mn3+ state.
    RSC Advances 08/2015; 5(83-83):67738-67741. DOI:10.1039/C5RA11628G · 3.84 Impact Factor
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    ABSTRACT: The Large sky Area Multi-Object Fiber Spectroscopic Telescope (LAMOST) general survey is a spectroscopic survey that will eventually cover approximately half of the celestial sphere and collect 10 million spectra of stars, galaxies and QSOs. Objects in both the pilot survey and the first year regular survey are included in the LAMOST DR1. The pilot survey started in October 2011 and ended in June 2012, and the data have been released to the public as the LAMOST Pilot Data Release in August 2012. The regular survey started in September 2012, and completed its first year of operation in June 2013. The LAMOST DR1 includes a total of 1202 plates containing 2 955 336 spectra, of which 1 790 879 spectra have observed signal-to-noise ratio (SNR) ≥ 10. All data with SNR ≥ 2 are formally released as LAMOST DR1 under the LAMOST data policy. This data release contains a total of 2 204 696 spectra, of which 1 944 329 are stellar spectra, 12 082 are galaxy spectra and 5017 are quasars. The DR1 not only includes spectra, but also three stellar catalogs with measured parameters: late A,FGK-type stars with high quality spectra (1061 918 entries), A-type stars (100 073 entries), and M-type stars (121 522 entries). This paper introduces the survey design, the observational and instrumental limitations, data reduction and analysis, and some caveats. A description of the FITS structure of spectral files and parameter catalogs is also provided. © 2015 National Astronomical Observatories, Chinese Academy of Sciences and IOP Publishing Ltd.
    Research in Astronomy and Astrophysics 08/2015; 15(8):1095-1124. DOI:10.1088/1674-4527/15/8/002 · 1.64 Impact Factor
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  • Xiaojie Wang · Jia Zhang · Lei Wang · Liang Deng ·
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    ABSTRACT: High-spin iron(II) alkynyl complexes [(IPr2Me2)2Fe(C≡CBut)2] (1) and [(IPr2Me2)2Fe(C≡CR)(NHMes)] (R = But 2, SiMe3 3) bearing a monodentate N-heterocyclic carbene ligand IPr2Me2 (1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene) have been prepared by salt metathesis and/or amine elimination methods and characterized by various spectroscopic methods. Complex 1 reacts with PMe3 (4 equiv) and ButNC (4 equiv) to form trans-[(PMe3)4Fe(C≡CBut)2] (4) and [η3-{(ButC≡C)(But)CC(IPr2Me2)C(NBut)}Fe(NCBut)3] (5), respectively. In contrast, the reactions of 1 with 4-Pri-C6H4NCO and PriNCNPri lead to the formation of the zwitterionic salts 4-Pri-C6H4NC(O)(IPr2Me2) and (PriN)2C(IPr2Me2), respectively. The interaction of 1 with I2 gives ButC≡CC≡CBut and (IPr2Me2)2FeI2. The C(sp)–C(sp3) cross-coupling products n-C8H17C≡CBut and c-C6H11C≡CBut are formed in high yields when 1 is treated with the corresponding alkyl halides n-C8H17X and c-C6H11X (X = Br, Cl). The formation of the ring-opening product 7,7-dimethyloct-1-en-5-yne in the reaction of 1 with cyclopropylmethyl bromide supports the radical character of the cross-coupling reaction.
    Organometallics 06/2015; 34(12):2775-2782. DOI:10.1021/acs.organomet.5b00028 · 4.13 Impact Factor

Publication Stats

2k Citations
527.67 Total Impact Points


  • 2014-2015
    • Shanghai Research Institute of Chemical Industry
      Shanghai, Shanghai Shi, China
    • Dalian Institute of Chemical Physics
      Lü-ta-shih, Liaoning, China
    • Jiangsu Provincial Center for Disease Control and Prevention
      Chiang-tu, Jiangsu Sheng, China
    • Hebei Medical University
      Chentow, Hebei, China
  • 2013-2015
    • Dalian University of Technology
      • DUT-KTH Joint Education and Research Center on Molecular Devices
      Lü-ta-shih, Liaoning, China
    • China Academy of Chinese Medical Sciences
      Peping, Beijing, China
    • 307 Hospital of the Chinese People's Liberation Army
      Peping, Beijing, China
    • National Space Science
      Peping, Beijing, China
  • 2010-2015
    • Anhui Agricultural University (AHAU)
      Luchow, Anhui Sheng, China
    • Wuhan Polytechnic University
      Wu-han-shih, Hubei, China
    • Zhejiang University
      • • State Key Lab of Rice Biology
      • • Department of Chemistry
      • • Institute of Insect Sciences
      Hang-hsien, Zhejiang Sheng, China
    • Shenyang University of Technology
      Feng-t’ien, Liaoning, China
    • China University of Petroleum
      • Department of Chemical Engineering
      Ch’ang-p’ing-ch’ü, Beijing, China
  • 2009-2015
    • Shandong University
      • Department of Chemical Engineering
      Chi-nan-shih, Shandong Sheng, China
  • 2006-2015
    • Chinese Academy of Sciences
      • • Shenzhen Institutes of Advanced Technology
      • • State Key Laboratory of Catalysis
      • • Key Laboratory of Applied Superconductivity
      • • Laboratory of Photosynthesis and Environmental Biology
      Peping, Beijing, China
  • 2011-2013
    • University Town of Shenzhen
      Shen-ch’üan-shih, Zhejiang Sheng, China
    • University of California, Berkeley
      • Department of Environmental Science, Policy, and Management
      Berkeley, California, United States
  • 2010-2013
    • Beijing Genomics Institute
      Bao'an, Guangdong, China
  • 2008-2013
    • East China Institute of Technology
      Yangkü, Shanxi Sheng, China
    • Beijing Normal University
      • State Key Laboratory of Remote Sensing Sciences
      Peping, Beijing, China
  • 2012
    • Saudi Academy
      Ar Riyāḑ, Ar Riyāḑ, Saudi Arabia
    • Nanfang Hospital
      Shengcheng, Guangdong, China
  • 2009-2010
    • Shenyang Institute of Technology
      Feng-t’ien, Liaoning, China
  • 2007
    • Technical Institute of Physics and Chemistry
      Peping, Beijing, China