罗平产生姜的化学成分

从生姜(Zingiber officinaleRosc.)的根茎中分离得一个骨架新颖的天然产物,经波谱鉴定为一个新的生姜内酯(1),同时分离得到7个已知化合物,分别为6-姜烯酚(2),1-去氢姜二酮(3),6-姜磺酸(4),3,5-二酮-1,7-二-{(3-甲氧基-4-羟基)-苯基}-庚烷(5),姜酮A(6),β-谷甾醇(7)和豆甾醇(8)。     

Onset of in vitro rhizogenesis response and peroxidase activity in Zingiber officinale (Zingiberaceae)

The induction of rooting in microshoots of Zingiber officinale cvs. Suprava, Turia local, Suruchi and V3S18 was achieved on half-strength basal Murashige and Skoog's medium supplemented with 0.5-1.0 mg/l either indole-3-acetic acid (IAA) or indole-3-butyric acid (IBA) and 2% (w/v) sucrose within 7-9 days of culture. Rooting was inhibited when the microshoots were cultured under higher concentration of auxins. The microshoots cultured on medium supplemented with NAA induced large number of thin root hairs with friable calluses within 6-7 days. Peroxidase activity was determined during root induction (0-day to the 10th day at every 2 day interval) from microshoots derived in vitro. The activity was minimum in the inductive phase (primary) and at the maximum level during the root initiative phase. These finding may be useful in monitoring the rooting behaviour in microshoots derived from different subculture and peroxidase activity as a marker for root initiation.     

Zingiber nanlingensis sp. nov. (Zingiberaceae) from Guangdong,China

Zingiber nanlingensis L. Chen, A. Q. Dong & F. W. Xing sp. nov. (Zingiberaceae) from northern Guangdong, China is described, illustrated, and compared with the morphologically similar species Z. mioga (Thunb.) Rosc.     

Pollen morphology and structure of Zingiber (Zingiberaceae)

The aim of the present study is to describe the morphology and internal wall structure of Zingiber pollen. The pollen of 18 species of Zingiber was examined by light, scanning and transmission electron microscopy. In the sections Zingiber and Dymczewiczia (Horan.) Benth. the pollen grains are spherical with cerebroid sculpturing while in the section Cryptanthium Horan. the pollen is ellipsoid with spira-striate sculpturing. All species have a thin coherent exine and an intine consisting of a thick, radially channeled outer layer and a thin, finely granular inner layer. On the basis of pollen morphology it is proposed that the section Dymczeniczia is included in the section Zingiber. The structure of the pollen wall in Zingiber resembles that of Canna and Strelitzia in having a pollen wall offering an infinite number of germination sites.     

Validation of Zingiber collinsii (Zingiberaceae) from Vietnam

The name Zingiber collinsii is validated and some corrections to an ealier publication are given.     

Characterization of polymorphic microsatellite markers,isolated from ginger (Zingiber officinale Rosc.)

The present study reports isolation and characterization of eight polymorphic microsatellite markers for Zingiber officinale Rosc. (Ginger). A total of 34 alleles were detected across the 20 accessions, with an average of 4.3 alleles per locus. Values for observed and expected heterozygosities ranged from 0 to 1.0 and from 0.23 to 0.67, respectively. The heterozygote deficits were observed at three loci. At the significance threshold (P < 0.05) of the eight loci, seven were found to have deviated from Hardy–Weinberg equilibrium, whereas significant linkage disequilibria were observed between 10 pairs of loci. Our data indicate the existence of moderate level of genetic diversity among the ginger accessions genotyped with eight markers.     

Five new species of Zingiber (Zingiberaceae) from Borneo

Recent collections from Sabah and Sarawak have revealed a wide species diversity among the Bornean members of the genus Zingiber. Four previously unknown and one incompletely known species of the genus are presented. Z. vinosum is a lowland species characterized by its burgundy colour of the lower surface of the leaves. Z. lambii was collected in primary lowland forest on ultramafic soil while Z. argenteum was collected in primary lowland forest on limestone. Both are characterized by their silvery leaves and orange inflorescences. Z. pendulum, found in primary mountain forest, has pending leafy stems and a deeply split labellum with very well developed side-lobes. Z. latifolium, found in secondary mountain forest, is vegetatively distinct by its broad leaves with a densely pubescent margin Z. vinosum, Z. Iambii, Z. pendulum and Z. latifolium are from Sabah and Z. argenteum is from Sarawak.     

Six new species of Zingiber (Zingiberaceae) from Borneo

Six new species of the genus Zingiber from Borneo are presented. Z viridiflavum was collected in primary lowland forest, while Z chlorobracteatum was collected in hilly secondary forest. Both are characterized by their slender fusiform inflorescences with yellow-green bracts. Z. flagelliforme found in primary lowland forest displays a peculiar reproduction habit in its tapering leafy shoots which bend over to trail on the ground where plantlets produced in the leaf-axis take root. Z velutinum was found in mid-elevation secondary forest. It is a tall plant with large ovate inflorescences and bright red, densely hairy bracts. Z phillippsii was found in a gulley in montane primary forest. It is vegetatively characterized by its purple stems and glabrous leaves while the inflorescence has a similarity to the common Bornean species Z. coloratum. Z. georgeii is distinct by its procumbent inflorescences with orange bracts. Z viridiflavum, Z. chlorobracteatum, Z. flagelliforme, Z. phillippsii and Z velutinum are from Sabah and Z georgeii is from Sarawak.     

A new species of Zingiber (Zingiberaceae) from Vietnam

Zingiber collinsii , a new species from Vietnam is described and illustrated. It is placed in section Zingiber having the inflorescence on a radical, short erect scape.     

Two new species of Zingiber (Zingiberaceae) from the Philippines

Zingiber banahaoense and Z. matutumense from the Philippines are described and illustrated.     

In vitro propagation of ginger (Zingiber officinale Rosco)

An efficient and promising protocol for in vitro propagation of Zingiber officinale Rosco using sprouting buds was established. Sprouting buds were sterilized and cultured onto MS medium supplemented with different growth regulators. Augmentation of MS-medium with 4.5 mg/l BAP recorded the highest percentage of shootlets multiplication. Shootlets were highly rooted on half strength of B₅ medium supplemented with 1.0 mg/l NAA. The maximum percentage of acclimatization, hardening and rhizomes production of in vitro derived plants in greenhouse was 80–100%.     

Taxonomic changes regarding three species of Zingiber (Zingiberaceae) from Thailand

Zingiber teres S. Q. Tong & Y. M. Xia and Z. xishuangbannaense S. Q. Tong are reduced to be synonyms of Z. smilesianum Craib and Z. thorelii Gagnep.,respectively. Z. cochinchinense Gagnep. is changed to be a subspecies of Z. zerumbet (L.) Sm.     

Volatile Flavor Components of ZINGIBERIS RHIZOMA (Zingiber officinale Roscoe)

The toxicity of dimethyl sulfoxide (Me₂SO) was examined in HeLa cells cultured at 37°C for up to 72 hr. The growth of the cells was measured by a colorimetric method with the use of 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), which gave good correlation between the cell number and the color development from the reduction of MTT under suitable conditions. When the initial number of cells was 3 × 10⁴/ml, Me₂SO at 1% or less had no apparent effect on prolifiration for up to 48 hr of incubation, but in longer incubations, cell growth was repressed. When the initial number of cells was 3 × 10⁵/ml, the effect of Me₂SO was similar.     

Metabolic profiling and phylogenetic analysis of medicinal Zingiber species: Tools for authentication of ginger (Zingiber officinale Rosc)

Phylogenetic analysis and metabolic profiling were used to investigate the diversity of plant material within the ginger species and between ginger and closely related species in the genus Zingiber (Zingiberaceae). In addition, anti-inflammatory data were obtained for the investigated species. Phylogenetic analysis demonstrated that all Zingiber officinale samples from different geographical origins were genetically indistinguishable. In contrast, other Zingiber species were significantly divergent, allowing all species to be clearly distinguished using this analysis. In the metabolic profiling analysis, the Z. officinale samples derived from different origins showed no qualitative differences in major volatile compounds, although they did show some significant quantitative differences in non-volatile composition, particularly regarding the content of [6]-, [8]-, and [10]-gingerols, the most active anti-inflammatory components in this species. The differences in gingerol content were verified by HPLC. The metabolic profiles of other Zingiber species were very different, both qualitatively and quantitatively, when compared to Z. officinale and to each other. Comparative DNA sequence/chemotaxonomic phylogenetic trees showed that the chemical characters of the investigated species were able to generate essentially the same phylogenetic relationships as the DNA sequences. This supports the contention that chemical characters can be used effectively to identify relationships between plant species. Anti-inflammatory in vitro assays to evaluate the ability of all extracts from the Zingiber species examined to inhibit LPS-induced PGE(2) and TNF-alpha production suggested that bioactivity may not be easily predicted by either phylogenetic analysis or gross metabolic profiling. Therefore, identification and quantification of the actual bioactive compounds are required to guarantee the bioactivity of a particular Zingiber sample even after performing authentication by molecular and/or chemical markers.     

Increasing in vitro microrhizome production of ginger (Zingiber officinale Roscoe)

In this study, using the quadratic saturation 310 D-optimal design method, we examined the effect of kinetin (KT), gibberellic acid (GA), and naphthalene acetic acid (NAA) on microrhizome production in ginger. The effect of GA on rhizome induction was larger than that of KT or NAA. Using simulation and optimality selection for tissue culture, we found that concentrations of GA, KT, and NAA of 1.33–2.35, 0.49–0.66, and 0.62 g/l, respectively, gave a microrhizome weight of over 0.25 g. The optimal conditions for microrhizome production were 80 g/l sucrose, 2 × MS macro-elements, and 1 × MS micro-elements, with a photoperiod of 24L:0D (light/dark). At the same time, 100% survival could be achieved on transfer of the in vitro ginger plantlets with microrhizomes to soil.     

A new species of Zingiber (Zingiberaceae) from Taiwan, China, based on morphological and molecular data

Zingiber shuanglongensis sp.nov.is a species endemic to Taiwan,China,that has been found in Nantou and Kaohsiung.In this study,the new Zingiber species is illustrated and the results of morphological a...     

Biosynthesis of curcuminoids and gingerols in turmeric (Curcuma longa) and ginger (Zingiber officinale): identification of curcuminoid synthase and hydroxycinnamoyl-CoA thioesterases

Members of the Zingiberaceae such as turmeric (Curcuma longa L.) and ginger (Zingiber officinale Rosc.) accumulate at high levels in their rhizomes important pharmacologically active metabolites that appear to be derived from the phenylpropanoid pathway. In ginger, these compounds are the gingerols; in turmeric these are the curcuminoids. Despite their importance, little is known about the biosynthesis of these compounds. This investigation describes the identification of enzymes in the biosynthetic pathway leading to the production of these bioactive natural products. Assays for enzymes in the phenylpropanoid pathway identified the corresponding enzyme activities in protein crude extracts from leaf, shoot and rhizome tissues from ginger and turmeric. These enzymes included phenylalanine ammonia lyase, polyketide synthases, p-coumaroyl shikimate transferase, p-coumaroyl quinate transferase, caffeic acid O-methyltransferase, and caffeoyl-CoA O-methyltransferase, which were evaluated because of their potential roles in controlling production of certain classes of gingerols and curcuminoids. All crude extracts possessed activity for all of these enzymes, with the exception of polyketide synthases. The results of polyketide synthase assays showed detectable curcuminoid synthase activity in the extracts from turmeric with the highest activity found in extracts from leaves. However, no gingerol synthase activity could be identified. This result was explained by the identification of thioesterase activities that cleaved phenylpropanoid pathway CoA esters, and which were found to be present at high levels in all tissues, especially in ginger tissues. These activities may shunt phenylpropanoid pathway intermediates away from the production of curcuminoids and gingerols, thereby potentially playing a regulatory role in the biosynthesis of these compounds.