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Identification of a self-regulatory pheromone system that controls nymph aggregation behavior of rice spittlebug Callitettix versicolor.

Frontiers in zoology

Chen X, Liang AP.
PMID: 25987889
Front Zool. 2015 May 17;12:10. doi: 10.1186/s12983-015-0102-4. eCollection 2015.

BACKGROUND: Nymphs of many spittlebug species are known to aggregate in one spittle mass, a behavior which greatly benefits the survival of the developing nymphs. Little is known, however, about the precise mechanisms that induce and regulate aggregation. Here,...

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Chen X, Liang AP. Identification of a self-regulatory pheromone system that controls nymph aggregation behavior of rice spittlebug Callitettix versicolor. Front Zool. 2015;12:10doi: 10.1186/s12983-015-0102-4.
Chen, X., & Liang, A. P. (2015). Identification of a self-regulatory pheromone system that controls nymph aggregation behavior of rice spittlebug Callitettix versicolor. Frontiers in zoology, 1210. https://doi.org/10.1186/s12983-015-0102-4
Chen, Xu, and Liang, Ai-Ping. "Identification of a self-regulatory pheromone system that controls nymph aggregation behavior of rice spittlebug Callitettix versicolor." Frontiers in zoology vol. 12 (2015): 10. doi: https://doi.org/10.1186/s12983-015-0102-4
Chen X, Liang AP. Identification of a self-regulatory pheromone system that controls nymph aggregation behavior of rice spittlebug Callitettix versicolor. Front Zool. 2015 May 17;12:10. doi: 10.1186/s12983-015-0102-4. eCollection 2015. PMID: 25987889; PMCID: PMC4435853.
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Evidence for stereoelectronic effects in the N-C-N group of 8,10,12-triaza-1-azoniatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane 4-nitrophenolate 4-nitrophenol monosolvate from the protonation of aminal (2R,7R)-1,8,10,12-tetraazatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane: X-ray and natural bond orbital analysis.

Acta crystallographica. Section C, Structural chemistry

Rivera A, Uribe JM, Ríos-Motta J, Osorio HJ, Bolte M.
PMID: 25836286
Acta Crystallogr C Struct Chem. 2015 Apr;71:284-8. doi: 10.1107/S2053229615004829. Epub 2015 Mar 14.

The title molecular salt, C11H21N4(+)·C6H4NO3(-)·C6H5NO3, (II), crystallizes with two independent three-component aggregates in the asymmetric unit. In the cations, the cyclohexane rings fused to the cage azaadamantane systems both adopt a chair conformation. In the crystal structure, the aggregates...

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Rivera A, Uribe JM, Ríos-Motta J, et al. Evidence for stereoelectronic effects in the N-C-N group of 8,10,12-triaza-1-azoniatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane 4-nitrophenolate 4-nitrophenol monosolvate from the protonation of aminal (2R,7R)-1,8,10,12-tetraazatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane: X-ray and natural bond orbital analysis. Acta Crystallogr C Struct Chem. 2015;71:284-8doi: 10.1107/S2053229615004829.
Rivera, A., Uribe, J. M., Ríos-Motta, J., Osorio, H. J., & Bolte, M. (2015). Evidence for stereoelectronic effects in the N-C-N group of 8,10,12-triaza-1-azoniatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane 4-nitrophenolate 4-nitrophenol monosolvate from the protonation of aminal (2R,7R)-1,8,10,12-tetraazatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane: X-ray and natural bond orbital analysis. Acta crystallographica. Section C, Structural chemistry, 71284-8. https://doi.org/10.1107/S2053229615004829
Rivera, Augusto, et al. "Evidence for stereoelectronic effects in the N-C-N group of 8,10,12-triaza-1-azoniatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane 4-nitrophenolate 4-nitrophenol monosolvate from the protonation of aminal (2R,7R)-1,8,10,12-tetraazatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane: X-ray and natural bond orbital analysis." Acta crystallographica. Section C, Structural chemistry vol. 71 (2015): 284-8. doi: https://doi.org/10.1107/S2053229615004829
Rivera A, Uribe JM, Ríos-Motta J, Osorio HJ, Bolte M. Evidence for stereoelectronic effects in the N-C-N group of 8,10,12-triaza-1-azoniatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane 4-nitrophenolate 4-nitrophenol monosolvate from the protonation of aminal (2R,7R)-1,8,10,12-tetraazatetracyclo[8.3.1.1(8,12).0(2,7)]pentadecane: X-ray and natural bond orbital analysis. Acta Crystallogr C Struct Chem. 2015 Apr;71:284-8. doi: 10.1107/S2053229615004829. Epub 2015 Mar 14. PMID: 25836286.
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[Raman spectroscopic studies of n-pentadecane under high temperature].

Guang pu xue yu guang pu fen xi = Guang pu

Qiao EW, Zheng HF.
PMID: 17390654
Guang Pu Xue Yu Guang Pu Fen Xi. 2007 Jan;27(1):78-80.

The present paper investigates the Raman spectrum of n-pentadecane in diamond anvil cell under a temperature up to 350 degrees C. The result shows that the pressure increases at elevated temperature, but the effect of pressure on the stretching...

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Qiao EW, Zheng HF. [Raman spectroscopic studies of n-pentadecane under high temperature]. Guang Pu Xue Yu Guang Pu Fen Xi. 2007;27(1):78-80
Qiao, E. W., & Zheng, H. F. (2007). [Raman spectroscopic studies of n-pentadecane under high temperature]. Guang pu xue yu guang pu fen xi = Guang pu, 27(1), 78-80.
Qiao, Er-wei, and Zheng, Hai-fei. "[Raman spectroscopic studies of n-pentadecane under high temperature]." Guang pu xue yu guang pu fen xi = Guang pu vol. 27,1 (2007): 78-80.
Qiao EW, Zheng HF. [Raman spectroscopic studies of n-pentadecane under high temperature]. Guang Pu Xue Yu Guang Pu Fen Xi. 2007 Jan;27(1):78-80. Chinese. PMID: 17390654.
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Ultrafast shock compression of self-assembled monolayers: a molecular picture.

The journal of physical chemistry. B

Patterson JE, Dlott DD.
PMID: 16863164
J Phys Chem B. 2005 Mar 24;109(11):5045-54. doi: 10.1021/jp045075u.

Simulations of self-assembled monolayers (SAMs) are performed to interpret experimental measurements of ultrafast approximately 1 GPa (volume compression deltaV approximately 0.1) planar shock compression dynamics probed by vibrational sum-frequency generation (SFG) spectroscopy (Lagutchev, A. S.; Patterson, J. E.; Huang,...

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Patterson JE, Dlott DD. Ultrafast shock compression of self-assembled monolayers: a molecular picture. J Phys Chem B. 2005;109(11):5045-54doi: 10.1021/jp045075u.
Patterson, J. E., & Dlott, D. D. (2005). Ultrafast shock compression of self-assembled monolayers: a molecular picture. The journal of physical chemistry. B, 109(11), 5045-54. https://doi.org/10.1021/jp045075u
Patterson, James E, and Dlott, Dana D. "Ultrafast shock compression of self-assembled monolayers: a molecular picture." The journal of physical chemistry. B vol. 109,11 (2005): 5045-54. doi: https://doi.org/10.1021/jp045075u
Patterson JE, Dlott DD. Ultrafast shock compression of self-assembled monolayers: a molecular picture. J Phys Chem B. 2005 Mar 24;109(11):5045-54. doi: 10.1021/jp045075u. PMID: 16863164.
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cis-Dichlorido(3,6,9-trithiabicyclo[9.3.1]pentadecane-κ2S3,S6)palladium(II) acetonitrile 0.8-solvate.

Acta crystallographica. Section C, Crystal structure communications

Dawe LN, Penney L, Black DA, Miller DO, Lucas CR.
PMID: 23832030
Acta Crystallogr C. 2013 Jul;69:727-9. doi: 10.1107/S0108270113015060. Epub 2013 Jun 14.

In the title complex, [PdCl2(C12H22S3)]·0.8CH3CN, a potentially tridentate thioether ligand coordinates in a cis-bidentate manner to yield a square-planar environment for the Pd(II) cation [mean deviation of the Pd from the Cl2S2 plane = 0.0406 (7) Å]. Each square-planar...

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Dawe LN, Penney L, Black DA, et al. cis-Dichlorido(3,6,9-trithiabicyclo[9.3.1]pentadecane-κ2S3,S6)palladium(II) acetonitrile 0.8-solvate. Acta Crystallogr C. 2013;69:727-9doi: 10.1107/S0108270113015060.
Dawe, L. N., Penney, L., Black, D. A., Miller, D. O., & Lucas, C. R. (2013). cis-Dichlorido(3,6,9-trithiabicyclo[9.3.1]pentadecane-κ2S3,S6)palladium(II) acetonitrile 0.8-solvate. Acta crystallographica. Section C, Crystal structure communications, 69727-9. https://doi.org/10.1107/S0108270113015060
Dawe, Louise Nicole, et al. "cis-Dichlorido(3,6,9-trithiabicyclo[9.3.1]pentadecane-κ2S3,S6)palladium(II) acetonitrile 0.8-solvate." Acta crystallographica. Section C, Crystal structure communications vol. 69 (2013): 727-9. doi: https://doi.org/10.1107/S0108270113015060
Dawe LN, Penney L, Black DA, Miller DO, Lucas CR. cis-Dichlorido(3,6,9-trithiabicyclo[9.3.1]pentadecane-κ2S3,S6)palladium(II) acetonitrile 0.8-solvate. Acta Crystallogr C. 2013 Jul;69:727-9. doi: 10.1107/S0108270113015060. Epub 2013 Jun 14. PMID: 23832030.
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Identification of major components of larviposition pheromone from larvae of tsetse fliesGlossina morsitans morsitans Westwood andGlossina morsitans centralis Machado.

Journal of chemical ecology

Saini RK, Hassanali A, Andoke J, Ahuya P, Ouma WP.
PMID: 24226080
J Chem Ecol. 1996 Jul;22(7):1211-20. doi: 10.1007/BF02266961.

The presence of pheromones produced by larvae ofGlossina morsitans morsitans andG. m. centralis, respectively, which attract gravid females and result in aggregation of pupae, is confirmed. Behavioral experiments indicated that females preferred to larviposit over moist sand conditioned by...

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Saini RK, Hassanali A, Andoke J, et al. Identification of major components of larviposition pheromone from larvae of tsetse fliesGlossina morsitans morsitans Westwood andGlossina morsitans centralis Machado. J Chem Ecol. 1996;22(7):1211-20doi: 10.1007/BF02266961.
Saini, R. K., Hassanali, A., Andoke, J., Ahuya, P., & Ouma, W. P. (1996). Identification of major components of larviposition pheromone from larvae of tsetse fliesGlossina morsitans morsitans Westwood andGlossina morsitans centralis Machado. Journal of chemical ecology, 22(7), 1211-20. https://doi.org/10.1007/BF02266961
Saini, R K, et al. "Identification of major components of larviposition pheromone from larvae of tsetse fliesGlossina morsitans morsitans Westwood andGlossina morsitans centralis Machado." Journal of chemical ecology vol. 22,7 (1996): 1211-20. doi: https://doi.org/10.1007/BF02266961
Saini RK, Hassanali A, Andoke J, Ahuya P, Ouma WP. Identification of major components of larviposition pheromone from larvae of tsetse fliesGlossina morsitans morsitans Westwood andGlossina morsitans centralis Machado. J Chem Ecol. 1996 Jul;22(7):1211-20. doi: 10.1007/BF02266961. PMID: 24226080.
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Dufour's gland and poison gland chemistry of the myrmicine ant,Messor capensis (Mayr).

Journal of chemical ecology

Brand JM, Mpuru SP.
PMID: 24249164
J Chem Ecol. 1993 Jul;19(7):1315-21. doi: 10.1007/BF00984878.

The Cape harvester ant,Messor capensis (Mayr), is widespread in the more arid regions of southern Africa, where it forms trails many meters long and harvests considerable quantities of seeds. The poison gland contains primarily the alkaloid, anabaseine, with minor...

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Brand JM, Mpuru SP. Dufour's gland and poison gland chemistry of the myrmicine ant,Messor capensis (Mayr). J Chem Ecol. 1993;19(7):1315-21doi: 10.1007/BF00984878.
Brand, J. M., & Mpuru, S. P. (1993). Dufour's gland and poison gland chemistry of the myrmicine ant,Messor capensis (Mayr). Journal of chemical ecology, 19(7), 1315-21. https://doi.org/10.1007/BF00984878
Brand, J M, and Mpuru, S P. "Dufour's gland and poison gland chemistry of the myrmicine ant,Messor capensis (Mayr)." Journal of chemical ecology vol. 19,7 (1993): 1315-21. doi: https://doi.org/10.1007/BF00984878
Brand JM, Mpuru SP. Dufour's gland and poison gland chemistry of the myrmicine ant,Messor capensis (Mayr). J Chem Ecol. 1993 Jul;19(7):1315-21. doi: 10.1007/BF00984878. PMID: 24249164.
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Alkane biosynthesis by Aspergillus carbonarius ITEM 5010 through heterologous expression of Synechococcus elongatus acyl-ACP/CoA reductase and aldehyde deformylating oxygenase genes.

AMB Express

Sinha M, Weyda I, Sørensen A, Bruno KS, Ahring BK.
PMID: 28058634
AMB Express. 2017 Dec;7(1):18. doi: 10.1186/s13568-016-0321-x. Epub 2017 Jan 05.

In this study we describe the heterologous expression of the recently identified cyanobacterial pathway for long chain alkane biosynthesis, involving the reduction of fatty acyl-ACP to fatty aldehyde and the subsequent conversion of this into alkanes, in the filamentous...

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Sinha M, Weyda I, Sørensen A, et al. Alkane biosynthesis by Aspergillus carbonarius ITEM 5010 through heterologous expression of Synechococcus elongatus acyl-ACP/CoA reductase and aldehyde deformylating oxygenase genes. AMB Express. 2017;7(1):18doi: 10.1186/s13568-016-0321-x.
Sinha, M., Weyda, I., Sørensen, A., Bruno, K. S., & Ahring, B. K. (2017). Alkane biosynthesis by Aspergillus carbonarius ITEM 5010 through heterologous expression of Synechococcus elongatus acyl-ACP/CoA reductase and aldehyde deformylating oxygenase genes. AMB Express, 7(1), 18. https://doi.org/10.1186/s13568-016-0321-x
Sinha, Malavika, et al. "Alkane biosynthesis by Aspergillus carbonarius ITEM 5010 through heterologous expression of Synechococcus elongatus acyl-ACP/CoA reductase and aldehyde deformylating oxygenase genes." AMB Express vol. 7,1 (2017): 18. doi: https://doi.org/10.1186/s13568-016-0321-x
Sinha M, Weyda I, Sørensen A, Bruno KS, Ahring BK. Alkane biosynthesis by Aspergillus carbonarius ITEM 5010 through heterologous expression of Synechococcus elongatus acyl-ACP/CoA reductase and aldehyde deformylating oxygenase genes. AMB Express. 2017 Dec;7(1):18. doi: 10.1186/s13568-016-0321-x. Epub 2017 Jan 05. PMID: 28058634; PMCID: PMC5216010.
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Microextraction of polycyclic aromatic hydrocarbons by using a stainless steel fiber coated with nanoparticles made from a porous aromatic framework.

Mikrochimica acta

Wang W, Li Z, Wang W, Zhang L, Zhang S, Wang C, Wang Z.
PMID: 29594554
Mikrochim Acta. 2017 Dec 05;185(1):20. doi: 10.1007/s00604-017-2577-5.

A porous aromatic framework of type PAF-6 was synthesized and explored as a coating onto a steel wire for using in solid-phase microextraction of polycyclic aromatic hydrocarbons (PAHs), phthalate plasticizers, and n-alkanes. The extraction temperature, extraction time, salt concentration,...

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Wang W, Li Z, Wang W, et al. Microextraction of polycyclic aromatic hydrocarbons by using a stainless steel fiber coated with nanoparticles made from a porous aromatic framework. Mikrochim Acta. 2017;185(1):20doi: 10.1007/s00604-017-2577-5.
Wang, W., Li, Z., Wang, W., Zhang, L., Zhang, S., Wang, C., & Wang, Z. (2017). Microextraction of polycyclic aromatic hydrocarbons by using a stainless steel fiber coated with nanoparticles made from a porous aromatic framework. Mikrochimica acta, 185(1), 20. https://doi.org/10.1007/s00604-017-2577-5
Wang, Wenchang, et al. "Microextraction of polycyclic aromatic hydrocarbons by using a stainless steel fiber coated with nanoparticles made from a porous aromatic framework." Mikrochimica acta vol. 185,1 (2017): 20. doi: https://doi.org/10.1007/s00604-017-2577-5
Wang W, Li Z, Wang W, Zhang L, Zhang S, Wang C, Wang Z. Microextraction of polycyclic aromatic hydrocarbons by using a stainless steel fiber coated with nanoparticles made from a porous aromatic framework. Mikrochim Acta. 2017 Dec 05;185(1):20. doi: 10.1007/s00604-017-2577-5. PMID: 29594554.
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Acetylenes in the Superbase-Promoted Assembly of Carbocycles and Heterocycles.

Accounts of chemical research

Trofimov BA, Schmidt EY.
PMID: 29668261
Acc Chem Res. 2018 May 15;51(5):1117-1130. doi: 10.1021/acs.accounts.7b00618. Epub 2018 Apr 18.

In this Account, we briefly discuss the recently discovered and rapidly developing superbase-promoted self-organization reactions of several equivalents of acetylenes and ketones to afford complex compounds that represent promising synthetic building blocks common in natural products. Notably, acetylenes play...

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Trofimov BA, Schmidt EY. Acetylenes in the Superbase-Promoted Assembly of Carbocycles and Heterocycles. Acc Chem Res. 2018;51(5):1117-1130doi: 10.1021/acs.accounts.7b00618.
Trofimov, B. A., & Schmidt, E. Y. (2018). Acetylenes in the Superbase-Promoted Assembly of Carbocycles and Heterocycles. Accounts of chemical research, 51(5), 1117-1130. https://doi.org/10.1021/acs.accounts.7b00618
Trofimov, Boris A, and Schmidt, Elena Yu. "Acetylenes in the Superbase-Promoted Assembly of Carbocycles and Heterocycles." Accounts of chemical research vol. 51,5 (2018): 1117-1130. doi: https://doi.org/10.1021/acs.accounts.7b00618
Trofimov BA, Schmidt EY. Acetylenes in the Superbase-Promoted Assembly of Carbocycles and Heterocycles. Acc Chem Res. 2018 May 15;51(5):1117-1130. doi: 10.1021/acs.accounts.7b00618. Epub 2018 Apr 18. PMID: 29668261.
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Populusene A, an Anti-inflammatory Diterpenoid with a Bicyclo[8,4,1]pentadecane Scaffold from .

Organic letters

Liu YY, Yan YM, Wang DW, Cheng YX.
PMID: 34794314
Org Lett. 2021 Nov 19;23(22):8657-8661. doi: 10.1021/acs.orglett.1c02378. Epub 2021 Aug 15.

Populusene A (

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Liu YY, Yan YM, Wang DW, et al. Populusene A, an Anti-inflammatory Diterpenoid with a Bicyclo[8,4,1]pentadecane Scaffold from . Org Lett. 2021;23(22):8657-8661doi: 10.1021/acs.orglett.1c02378.
Liu, Y. Y., Yan, Y. M., Wang, D. W., & Cheng, Y. X. (2021). Populusene A, an Anti-inflammatory Diterpenoid with a Bicyclo[8,4,1]pentadecane Scaffold from . Organic letters, 23(22), 8657-8661. https://doi.org/10.1021/acs.orglett.1c02378
Liu, Yun-Yun, et al. "Populusene A, an Anti-inflammatory Diterpenoid with a Bicyclo[8,4,1]pentadecane Scaffold from ." Organic letters vol. 23,22 (2021): 8657-8661. doi: https://doi.org/10.1021/acs.orglett.1c02378
Liu YY, Yan YM, Wang DW, Cheng YX. Populusene A, an Anti-inflammatory Diterpenoid with a Bicyclo[8,4,1]pentadecane Scaffold from . Org Lett. 2021 Nov 19;23(22):8657-8661. doi: 10.1021/acs.orglett.1c02378. Epub 2021 Aug 15. PMID: 34794314.
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Alkane-priming of Beauveria bassiana strains to improve biocontrol of the redbanded stink bug Piezodorus guildinii and the bronze bug Thaumastocoris peregrinus.

Journal of invertebrate pathology

Sessa L, Pedrini N, Altier N, Abreo E.
PMID: 34838792
J Invertebr Pathol. 2021 Nov 26;187:107700. doi: 10.1016/j.jip.2021.107700. Epub 2021 Nov 26.

Insect epicuticle hydrocarbons (CHC) are known to be important determinants in the susceptibility degree of insects to fungal entomopathogens. Five Beauveria bassiana (Balsamo) Vuillemin (Hypocreales; Clavicipitaceae) strains were phenotypically analyzed regarding their response to CHC nutrition and their pathogenicity...

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Sessa L, Pedrini N, Altier N, et al. Alkane-priming of Beauveria bassiana strains to improve biocontrol of the redbanded stink bug Piezodorus guildinii and the bronze bug Thaumastocoris peregrinus. J Invertebr Pathol. 2021;187:107700doi: 10.1016/j.jip.2021.107700.
Sessa, L., Pedrini, N., Altier, N., & Abreo, E. (2021). Alkane-priming of Beauveria bassiana strains to improve biocontrol of the redbanded stink bug Piezodorus guildinii and the bronze bug Thaumastocoris peregrinus. Journal of invertebrate pathology, 187107700. https://doi.org/10.1016/j.jip.2021.107700
Sessa, Lucía, et al. "Alkane-priming of Beauveria bassiana strains to improve biocontrol of the redbanded stink bug Piezodorus guildinii and the bronze bug Thaumastocoris peregrinus." Journal of invertebrate pathology vol. 187 (2021): 107700. doi: https://doi.org/10.1016/j.jip.2021.107700
Sessa L, Pedrini N, Altier N, Abreo E. Alkane-priming of Beauveria bassiana strains to improve biocontrol of the redbanded stink bug Piezodorus guildinii and the bronze bug Thaumastocoris peregrinus. J Invertebr Pathol. 2021 Nov 26;187:107700. doi: 10.1016/j.jip.2021.107700. Epub 2021 Nov 26. PMID: 34838792.
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