[ Objective] Effects of sub-chronic intoxication of 1,8-cineole on body weights, routine blood indexes and biochemical indexes of mice were investigated. [Method] One hundred and sixty mice with body weights of 15 -17...[ Objective] Effects of sub-chronic intoxication of 1,8-cineole on body weights, routine blood indexes and biochemical indexes of mice were investigated. [Method] One hundred and sixty mice with body weights of 15 -17 g were randomly divided into four groups （forty mice per group）. Mice were injected to 1, 8 - cineole with doses of 192.45,64. 15 and 21.38 mg/kg body weight （ test groups） and the water solution of tween-80 with a volume fraction of 0.5% （ control group） respectively. Each mouse was administered orally at the dose of 0.2 mL per 10 g body weight once a day consecutively for 90 d. The body weight, routine blood indexes and serum biochemical indexes of mice were determined on the 30^th d, 60^th d, 90^th d and the 30^th d after stopping the administration of 1,8-cineole. [ Result] The effects of 1, 8-cineole on the body weight, routine blood indexes and serum biochemical indexes of mice with the doses of 64.15 and 21.38 mg/kg body weight had no statistically significant difference compared with the control group （P 〉0.05 ）. 1, 8-cineole with the dose of 192.45 mg/kg body weight exhibited different influences on routine blood indexes and serum biochemical indexes of mice after the oral administration of 1,8-cineole for 60 d and 90 d, and statistically significant differences in many blood biochemical indexes were observed （P 〈 0.05 ）. However, the differences in routine blood indexes and serum biochemical indexes were not statistically significant between the test groups and the control group at the 30＇h d after stopping the administration of 1, 8-cineole （ P 〉 0.05）. [Condusion] 1,8-cineole had sub-chronic oral toxicity to mice. The no observed adverse effect level （NOAEL） of 1,8-cineolc was 64.15 mg/kg body weight and the lowest observed adverse effect level （LOAEL） of 1,8-cineole was 192.45 mg/kg body weight. Effects of 1, 8-cineole on blood biochemical indexes of mice were in short term and reversible.展开更多
An endophytic fungus producing 1,8-cineole from Neolitsea pulchella (Meissn.) Merr. was identified as Annulohypoxylon sp. by phylogenetic analyses of the sequence alignments of ITS rDNA, β-tubulin, Actin and EF1-α. ...An endophytic fungus producing 1,8-cineole from Neolitsea pulchella (Meissn.) Merr. was identified as Annulohypoxylon sp. by phylogenetic analyses of the sequence alignments of ITS rDNA, β-tubulin, Actin and EF1-α. This isolate produces an attractive spectrum of volatile organic compounds (VOCs) with only one dominant component, 1,8-cineole, as identified by gas chromatography-mass spectrometry (GC-MS). The fungus was able to grow in seven media with different carbon sources, and five raw agro-forest residues. The content of 1,8-cineole in the mixed VOCs via fungus reached up to 94.95% and 91.25% relative area in PDA and raw poplar sawdust, respectively. Under optimum test conditions, the fungus produced 1,8-cineole at the 0.764 ppmv in 50 mL head spaces in PDA. Interestingly, 1,8-cineole is an ideal fuel additive for both diesel and gasoline engines. Also, this is the first isolate, in this group of fungi, making cineole, which produces as its primary VOC product which makes it an ideal organism for strain improvement. Such as step will be critical for its ultimate use in biofuel production.展开更多
Nicotiana species of the section Alatae characteristically emit the floral scent compounds of the ＇cineole cassette＇ comprising 1,8-cineole, limonene, myrcene, α-pinene, β-pinene, sabinene, and α-terpineol. We su...Nicotiana species of the section Alatae characteristically emit the floral scent compounds of the ＇cineole cassette＇ comprising 1,8-cineole, limonene, myrcene, α-pinene, β-pinene, sabinene, and α-terpineol. We successfully isolated genes of Nicotiana alata and Nicotiana langsdorfii that encoded enzymes, which produced the characteristic monoter- penes of this ＇cineole cassette＇ with α-terpineol being most abundant in the volatile spectra. The amino acid sequences of both terpineol synthases were 99% identical. The enzymes cluster in a monophyletic branch together with the closely related cineole synthase of Nicotiana suaveolens and monoterpene synthase 1 of Solanum lycopersicum. The cyclization reactions （α-terpineol to 1,8-cineole） of the terpineol synthases of N. alata and N. langsdorfii were less efficient compared to the ＇cineole cassette＇ monoterpene synthases of Arabidopsis thaliana, N. suaveolens, Salvia fruticosa, Salvia officinalis, and Citrus unshiu. The terpineol synthases of IV. alata and N. langsdorfii were localized in pistils and in the adaxial and abaxial epidermis of the petals. The enzyme activities reached their maxima at the second day after anthesis when flowers were fully opened and the enzyme activity in N. alata was highest at the transition from day to night （diurnal rhythm）.展开更多
We used 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol（A） as the host molecule to selectively recognize the component 1,8-cineole（B） in the volatile oil of Flos Magnoliae（Xin Yi）. The inclusion compound（A+B） was f...We used 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol（A） as the host molecule to selectively recognize the component 1,8-cineole（B） in the volatile oil of Flos Magnoliae（Xin Yi）. The inclusion compound（A+B） was formed as crystalline, and the structure was confirmed by means of IR, （（）1H NMR）, and single crystal X-ray diffraction, with the 1∶2 molar ratios of the host to the guest. The component 1,8-cineole（B） was selectively isolated from the inclusion compound（A+B） by Kugelrohr vaccum technology, and then further characterized by IR, （）1H NMR and （）13C NMR. The whole components in the volatile oil of Flos Magnoliae（Xin Yi） and the isolation effect of 1,8-cineole isolated from inclusion crystals were analyzed by GC and GC-MS, respectively. The result indicate that the good isolation effect is given by the inclusion method, with purity and yield of the component 1,8-cineole（B） separated from the volatile oil of Flos Magnoliae are 100% and 85%, respectively.展开更多
基金Supported by the Incubation Program for Science and Technology Innovative Research Team in Sichuan Province of China(2011-JTD0035)Program of Department of Education in Sichuan Province of China(10ZB050)the Program of Department of Education in Sichuan Province of China(11ZZ022)
文摘[ Objective] Effects of sub-chronic intoxication of 1,8-cineole on body weights, routine blood indexes and biochemical indexes of mice were investigated. [Method] One hundred and sixty mice with body weights of 15 -17 g were randomly divided into four groups （forty mice per group）. Mice were injected to 1, 8 - cineole with doses of 192.45,64. 15 and 21.38 mg/kg body weight （ test groups） and the water solution of tween-80 with a volume fraction of 0.5% （ control group） respectively. Each mouse was administered orally at the dose of 0.2 mL per 10 g body weight once a day consecutively for 90 d. The body weight, routine blood indexes and serum biochemical indexes of mice were determined on the 30^th d, 60^th d, 90^th d and the 30^th d after stopping the administration of 1,8-cineole. [ Result] The effects of 1, 8-cineole on the body weight, routine blood indexes and serum biochemical indexes of mice with the doses of 64.15 and 21.38 mg/kg body weight had no statistically significant difference compared with the control group （P 〉0.05 ）. 1, 8-cineole with the dose of 192.45 mg/kg body weight exhibited different influences on routine blood indexes and serum biochemical indexes of mice after the oral administration of 1,8-cineole for 60 d and 90 d, and statistically significant differences in many blood biochemical indexes were observed （P 〈 0.05 ）. However, the differences in routine blood indexes and serum biochemical indexes were not statistically significant between the test groups and the control group at the 30＇h d after stopping the administration of 1, 8-cineole （ P 〉 0.05）. [Condusion] 1,8-cineole had sub-chronic oral toxicity to mice. The no observed adverse effect level （NOAEL） of 1,8-cineolc was 64.15 mg/kg body weight and the lowest observed adverse effect level （LOAEL） of 1,8-cineole was 192.45 mg/kg body weight. Effects of 1, 8-cineole on blood biochemical indexes of mice were in short term and reversible.
文摘An endophytic fungus producing 1,8-cineole from Neolitsea pulchella (Meissn.) Merr. was identified as Annulohypoxylon sp. by phylogenetic analyses of the sequence alignments of ITS rDNA, β-tubulin, Actin and EF1-α. This isolate produces an attractive spectrum of volatile organic compounds (VOCs) with only one dominant component, 1,8-cineole, as identified by gas chromatography-mass spectrometry (GC-MS). The fungus was able to grow in seven media with different carbon sources, and five raw agro-forest residues. The content of 1,8-cineole in the mixed VOCs via fungus reached up to 94.95% and 91.25% relative area in PDA and raw poplar sawdust, respectively. Under optimum test conditions, the fungus produced 1,8-cineole at the 0.764 ppmv in 50 mL head spaces in PDA. Interestingly, 1,8-cineole is an ideal fuel additive for both diesel and gasoline engines. Also, this is the first isolate, in this group of fungi, making cineole, which produces as its primary VOC product which makes it an ideal organism for strain improvement. Such as step will be critical for its ultimate use in biofuel production.
文摘Nicotiana species of the section Alatae characteristically emit the floral scent compounds of the ＇cineole cassette＇ comprising 1,8-cineole, limonene, myrcene, α-pinene, β-pinene, sabinene, and α-terpineol. We successfully isolated genes of Nicotiana alata and Nicotiana langsdorfii that encoded enzymes, which produced the characteristic monoter- penes of this ＇cineole cassette＇ with α-terpineol being most abundant in the volatile spectra. The amino acid sequences of both terpineol synthases were 99% identical. The enzymes cluster in a monophyletic branch together with the closely related cineole synthase of Nicotiana suaveolens and monoterpene synthase 1 of Solanum lycopersicum. The cyclization reactions （α-terpineol to 1,8-cineole） of the terpineol synthases of N. alata and N. langsdorfii were less efficient compared to the ＇cineole cassette＇ monoterpene synthases of Arabidopsis thaliana, N. suaveolens, Salvia fruticosa, Salvia officinalis, and Citrus unshiu. The terpineol synthases of IV. alata and N. langsdorfii were localized in pistils and in the adaxial and abaxial epidermis of the petals. The enzyme activities reached their maxima at the second day after anthesis when flowers were fully opened and the enzyme activity in N. alata was highest at the transition from day to night （diurnal rhythm）.
文摘We used 1,1,6,6-tetraphenylhexa-2,4-diyne-1,6-diol（A） as the host molecule to selectively recognize the component 1,8-cineole（B） in the volatile oil of Flos Magnoliae（Xin Yi）. The inclusion compound（A+B） was formed as crystalline, and the structure was confirmed by means of IR, （（）1H NMR）, and single crystal X-ray diffraction, with the 1∶2 molar ratios of the host to the guest. The component 1,8-cineole（B） was selectively isolated from the inclusion compound（A+B） by Kugelrohr vaccum technology, and then further characterized by IR, （）1H NMR and （）13C NMR. The whole components in the volatile oil of Flos Magnoliae（Xin Yi） and the isolation effect of 1,8-cineole isolated from inclusion crystals were analyzed by GC and GC-MS, respectively. The result indicate that the good isolation effect is given by the inclusion method, with purity and yield of the component 1,8-cineole（B） separated from the volatile oil of Flos Magnoliae are 100% and 85%, respectively.
