红参加工中皂苷的脱羧降解反应及其产物的研究

从鲜人参中提取分离出天然皂苷,模拟红参加工工艺过程,探讨红参加工中天然皂苷成分转化过程,以揭示出皂苷成分转化机理。方法：将红参粉以甲醇提取,乙醚脱脂,正丁醇萃取;水层通过大孔树脂（Ｄ１０１型）吸附,水洗除去水溶性发质和糖分。再经过硅胶柱层析和阳离子交换树脂柱层析,获得丙二酸单酰基人参皂苷。模拟红参加工工艺过程得转化物,对该转化物进行分离鉴定,诸如化学试验、ＩＲ、ＦＤ－ＭＳ等仪器分析。结果表明：从鲜人参中分离出丙二酸单酰基人参皂苷－Ｒｂ２和－Ｒｂ２等皂苷,通过模拟红参加工试验发现在７５℃烘干过程,丙二酸单酰基人参皂苷－Ｒｂ２转化为乙酰基人参皂苷－Ｒｂ２,即人参皂苷Ｒｓ１。结论：人参皂苷Ｒｓ１是红参加工烘干阶段产生的,对其分解产物的分析有二氧化碳放出,说明该反应是丙二酸单酰基人参皂苷上的丙二元到遇热发生脱羧降解反应     

Evaluation of rice allelopathy in hydroponics

The inhibitory activity of water extracts from the shoots and roots of three rice cultivars, Taichung native 1 (TN1) and IAC165 (both allelopathic rice) and AUS196 (non-allelopathic rice), grown in hydroponics was evaluated. The release of germination inhibitors by allelopathic rice plants into hydroponic solution was also determined with freshly collected solution and XAD-4 resin desorbate. The degree of the inhibition was quantified in terms of root growth in Echinochloa colona, Echinochloa crus-galli, Echinochloa crus-galli var. oryzicola, Triantema portulacastrum and Lactuca sativa. The allelopathic activity of rice was species specific, and depended on source and concentration. Root length of all test species was inhibited by the different concentrations of shoot extract of allelopathic and non-allelopathic rice. However, of the three cultivars, TN1 showed higher inhibition than IAC165 and AUS196 in all test species. Water extracts of shoots and roots significantly inhibited root growth in E. crus-galli but the shoot extract gave a greater inhibitory effect on E. crus-galli than the root extract. Root exudate of TN1 inhibited root elongation of E. crus-galli from 2 weeks after transplanting (WAT) and the inhibition continued for 4 WAT. The results confirmed the previous finding of a laboratory bioassay that the TN1 had allelopathic activity and produced allelochemicals that inhibit growth of some weed species.     

Genetic variation detected with random amplified polymorphicDNA markers among isolates of the red rot disease fungus Pythiumporphyrae isolated from Porphyra yezoensis from Koreaand Japan

ABSTRACT:   Genetic variation of the fungal parasite Pythium porphyrae ,causative organism of red rot disease of Porphyra , isolatedfrom Asan, Mokpo, Pusan and Wando in Korea, and from Aichi, Fukuokaand Miyagi in Japan was investigated by random amplified polymorphicDNA (RAPD) cluster analysis. The total 67 RAPD markers were generatedfrom 38 isolates by RAPD-polymerase chain reaction (PCR) using arbitraryprimers consisting of 10 nucleotide sequences and 33 of them indicatedpolymorphisms. The dissimilarity coefficients calculated from theRAPD banding patterns ranged from 0.0010 to 0.6983. The dendrogramgenerated by the unweighted pair-group method using arithmetic averagesshowed that the 38 isolates were classified into three clusters(Groups 1, 2 and 3). Group 1 consisting of two isolates from Miyagiwas separated from all other isolates by a genetic distance of 0.6983.Groups 2 and 3 containing the majority of the isolates were branchedon genetic distance of 0.3957. These two clusters subdivided intofour and three subclusters, respectively, which were apparentlyassociated with geographic origins of the isolates. Interestingly,the isolates from Asan of Korea were close to Japanese isolatesrather than Korean isolates on genetic diversity. In addition, thegenetic distances of intra-isolates from Japan were higher thanthose from Korea.     

COMPUTED TOMOGRAPHIC APPEARANCE OF PRIMARY LUNG TUMORS IN DOGS

Canine primary lung tumors typically appear radiographically as a well‐circumscribed solitary mass in the periphery of a caudal lung lobe. Consolidated and diffuse forms of primary lung tumors have also been described. Nineteen dogs with computed tomographic (CT) images of the thorax and a histological diagnosis of primary lung tumor (17 primary carcinomas and two primary sarcomas) were evaluated retrospectively to characterize the CT findings. All primary lung tumors were bronchocentric in origin with internal air bronchograms. The bronchi were typically narrowed, displaced, and often obstructed by the tumor. Eighteen of 19 (95%) of the tumors were solitary and there was one pneumonic/alveolar form. Most solitary tumors were well circumscribed (17/18), located in the central to periphery of the lung (14/18), and in a cranial or caudal lobe (16/19). Most primary lung tumors (11/17) had mild to moderate heterogeneous contrast enhancement. Five of 19 dogs (26%) had evidence of pulmonary metastasis. Internal mineralization (3/19) and tracheobronchial lymphadenopathy (4/19) were also identified. On CT examination, solitary, well circumscribed, bronchocentric masses with internal air bronchograms are consistent with a primary pulmonary tumor in dogs.     

SLA typing using the PCR‐SSP method and establishment of the SLA homozygote line in pedigreed SNU miniature pigs

Seoul National University (SNU) miniature pigs represent a closed colony with 24 founder pigs and a well preserved pedigree. Characterization using mRNA sequence analysis was conducted for 6 swine leukocyte antigen (SLA) loci in parental or founder pigs, and 17 defined alleles were detected. Based on these complete coding sequences, 17 sequence specific primers (SSPs) were designed for polymorphic sites. To validate the specificity of each allele SSP, the PCR‐SSP was conducted with defined allele clones as templates. PCR‐SSP was conducted with the hot start polymerase and touch‐down PCR. The parental or found SNU miniature pigs showed overall SLA class I and II heterozygotes. Using the established PCR‐SSP method, we conducted SLA typing for breeding stock including 2 pedigreed pigs and identified the novel SLA class II homozygote haplotye (DRA*0201, DRB1*0403, DQA*0102 and DQB1*0701) and 2 SLA homozygote pig lines: SLA class I Hp‐3.0 and class II Hp‐0.3, and SLA class I Hp‐2.0 and class II Hp‐0.2. We thought that our PCR‐SSP SLA typing method could be applicable for new SLA homozygote line establishment by assignment and scheduled breeding.