吉林省人参种植产业发展对策分析

随着人参种植产业链的不断延展,人参种植业最终将形成融合了先进现代技术和设备 的产业集群。传统生产技术和加工技术形成的产业链系统由于生产管理方法分散,技术水平 低,人参质量低,规模小,产品经济特性不断追求微薄的利润,存在着诸多的发展问题,因此需要 按照现代产业链发展模式进行改造。本研究综合吉林省人参种植产业发展的现状,对于吉林省 人参种植产业未来的发展对策进行了简要的分析。研究结论对于改善吉林省人参种植产业发 展现状具有重要意义。     

胍盐聚合物添加量对抗菌食品包装膜抗菌性及物理性能的影响

为了开发出一种安全高效的抗菌食品包装材料,添加不同质量分数(0～7%)的聚六亚甲基双胍盐酸盐(polyhexamethylene biguanidine hydrochloride,PHMB)抗菌母粒到聚乙烯基材中,制成PHMB抗菌膜,比较PHMB母粒添加量对抗菌食品包装薄膜的抗菌性和性能的影响。结果表明,随着PHMB母粒添加量的增大,薄膜抗菌性增强。PHMB母粒添加量为4%时,薄膜对大肠杆菌、金黄色葡萄球菌和杂菌样品的抗菌率分别为99.1%、99.2%和83.4%,且存放6个月后薄膜仍保持较强的抗菌作用;添加PHMB母粒后,薄膜的透光率、水蒸气透过率影响较小;薄膜的力学性能在PHMB母粒添加量为4%时最优;PHMB(4%)抗菌膜对实际试样(鳕鱼干)表现出良好的微生物抑制作用。因此,确定抗菌薄膜中PHMB母粒最佳添加量为4%,薄膜具备强抗菌作用和良好的性能。该研究为抗菌材料的研制提供了参考。     

Identification of a novel variant lacking group A soyasaponin in a Chinese wild soybean (Glycine soja Sieb. & Zucc.): implications for breeding significance

Group A saponins are the principal factors underlying the undesirable bitter and astringent tastes in soybean food products. Therefore, the genetic reduction or elimination of the undesirable tastes is of great significance in soybean taste breeding. Using thin‐layer chromatography and liquid chromatography–mass spectrometry, we identified a novel mutant lacking group A saponins in a wild soybean (Glycine soja Sieb. & Zucc.), reflecting the failed arabinose binding of arabinosyltransferase to the C‐22 hydroxyl group, consequently leading to a lack of group A saponins and the concomitance expression of two new components A‐αg and KA‐αg in seeds. The C‐3 glycosylated soyasapogenol A (SS‐A), A‐αg, is a steady precursor compound in biosynthesis of Aa and Ab types in the seeds of soybean plants and exhibits stable inheritance. In this study, we observed a critical step necessary for arabinose binding to the C‐22 hydroxyl group in the biosynthetic pathway of group A saponins and identified an important germplasm accession for the genetic improvement in the tastes of soybean milk and processed soybean foods.     

Effect of intramammary infusion of recombinant bovine GM-CSF and IL-8 on CMT score,somatic cell count,and milk mononuclear cell populations in Holstein cows with <Emphasis Type="Italic">Staphylococcus aureus</Emphasis> subclinical mastitis

The effect of intramammary infusion of recombinant bovine granulocyte-macrophage colony-stimulating factor (rbGM-CSF) and interleukin-8 (rbIL-8) on mononuclear cell populations in quarters, somatic cell count (SCC) and the California Mastitis Test (CMT) score were investigated. From the selected cows with naturally occurring Staphylococcus aureus subclinical mastitis, one quarter of each cow were selected for the infusions of rbGM-CSF (400 μg/5 mL/quarter, n = 9), rbIL-8 (1 mg/5 mL/quarter, n = 9), and phosphate-buffered saline (5 mL/quarter, n = 7). The CMT score of both cytokines post infusion temporarily increased between days 0 and 1 and significantly decreased between days 7 and 14 compared to the preinfusion level. The SCC on day 14 after infusions of rbGM-CSF tended to be lower than that of the control group. The percentage of CD14+ cells increased on days 1 and 2 post infusion of rbGM-CSF. The percentage of CD4+ and CD8+ cells also increased on days 2 and 3, suggesting that the infusion of rbGM-CSF enhanced cellular immunity in the mammary gland. In contrast, the percentage of CD14+ cells decreased on days 0.25 and 1 post infusion of rbIL-8. No significant changes in the percentages of CD4+ and CD8+ cells in milk after infusion of rbIL-8 were evident during the experimental period, which suggested that rbIL-8 had little effect on the function of T cells in the mammary gland. These results indicated that rbGM-CSF and rbIL-8 decreased the CMT score by a different mechanism and may have a potential as therapeutic agents for subclinical mastitis.     

Dietary supplement of G-rutin reduces oxidative damage in the rodent model.

Dietary supplement of bioflavonoid rutin and calorie restriction were examined to investigate possible reduction in oxidative DNA damage, protein oxidation, and lipid peroxidation in animals. Rats were fed ad libitum 20% casein semipurified diet or a diet that was supplemented by 2.5% water soluble rutin derivative, 4(G)-alpha-glucopyranosylrutin (G-rutin) for 18 days. Two other groups of rats were fed the respective diets at 60% of the mean food intake of the ad libitum fed animals for the same period. Urinary excretion of thymine glycol and thymidine glycol, indices of DNA base damage in the whole body, were significantly low in the G-rutin-supplemented groups. The protein carbonyl contents, a measure of protein oxidation, were significantly low in the liver of G-rutin-supplemented groups and calorie-restricted groups. The data indicate that G-rutin provides an antioxidant defense in rodents against free radical-caused oxidative damage of DNA and proteins.     

Long-term Pulmonary Responses to Quadweekly Intermittent Intratracheal Spray Instillations of Magnetite (Fe3O4) Nanoparticles for 52 Weeks in Fischer 344 Rats

Information about potential risks of iron nanomaterials is still limited, while a wide variety of applications are expected. We recently reported acute phase responses of male and female Fischer 344 rats after a single intratracheal spray instillation of Fe₃O₄ nanoparticles (magnetite), clearly showing dose-dependent pulmonary inflammatory changes (Tada et al., J Toxicol Pathol 25, 233–239, 2012). The present study assessed long-term responses of male and female Fischer 344 rats to multiple administrations of magnetite. Ten-week-old male and female Fischer 344 rats (n=20/group) were exposed to a total of 13 quadweekly intermittent intratracheal spray instillations of magnetite during the experimental period of 52 weeks, at doses of 0, 0.2 (low), 1.0 (medium) and 5.0 (high-dose) mg/kg body weight per administration. Absolute and relative lung weights of the high-dose group were significantly higher than those of the control group. Macroscopically, slight enlargement and scattered black patches were recognized in the lungs and the lung-associated lymph nodes of the high-dose group. Histopathologically, infiltration of macrophages phagocytosing magnetite (all dose groups) and of chronic inflammatory cells (medium- and high-dose males and high-dose females), alveolar bronchiolization and granuloma (high-dose group) were observed. In addition, alveolar hyperplasias were observed in some rats of the high-dose group, and cytoplasmic overexpression of β-catenin protein was immunohistochemically found in such lesions. The present results clearly show that instilled magnetite causes chronic inflammatory responses in the lung. These responses occur in a dose-dependent manner without apparent differences among sexes     

Feeding of the short-spined sea urchin <Emphasis Type="Italic">Strongylocentrotus intermedius</Emphasis> on macroalgae and benthic animals

To examine the feeding ecology of the sea urchin Strongylocentrotus intermedius, two types of macroalgal diet (kelp Saccharina longissima and red alga Ptilota filicina) and four types of benthic animal diet [barnacle Balanus glandula, limpet Lottia cassis, free-living Perinereis aibuhitensis and P. aibuhitensis attached to a stainless steel wire (wired polychaete)], were separately or simultaneously provided for urchins of 5- to 60-mm test diameter (TD). Sea urchins of even 3-mm TD could graze the kelp, and began to graze the red alga, the wired polychaete and limpet by 5-mm TD, the barnacle by 8-mm TD and the free-living polychaete by 15-mm TD, respectively. These results suggest that the variety of macroalgae and benthic animals which the urchin can graze increases with the ontogeny of their feeding organs, motility and ability to catch animals. Both juvenile and adult sea urchins preferred to eat the polychaete as well as the kelp fronds. Feed conversion efficiency and daily growth rate of the small sea urchins fed benthic animals like the polychaete were higher than those fed macroalgae. The sea urchins are likely to grow better when feeding on animals than on macroalgae, even in habitats where they can access adequate quantities of kelp.     

Comparative study on general properties of alginate lyases from some marine gastropod mollusks

Alginate lyase (EC 4.2.2.3) is an enzyme that splits glycosyl linkages of alginate chain via β-elimination, producing unsaturated oligoalginates. This enzyme is widely distributed in herbivorous marine mollusks, brown algae, and marine and soil bacteria. In the present study, we determined the general properties and partial amino acid sequences of alginate lyases from three Archeogastropoda, i.e., Haliotis discus hannai, H. iris, and Omphalius rusticus, and one Mesogastropoda, i.e., Littorina brevicula, in order to enrich the information about functional and structural diversity in gastropod alginate lyases. The alginate lyases were extracted from hepatopancreas of these animals and purified by ammonium sulfate fractionation followed by conventional column chromatography. Single alginate lyases with molecular masses of approximately 28, 34, and 34 kDa were isolated from H. discus, H. iris, and O. rusticus, respectively. While three alginate lyases with molecular masses of 35, 32, and 28 kDa were isolated from L. brevicula. These enzymes were identified as poly(M) lyase (EC 4.2.2.3) since they preferably degraded poly(M)-rich substrate. Western blot analysis using an antiserum raised against H. discus enzyme suggested that H. iris, and O. rusticus enzymes shared similar primary/higher-order structure with H. discus enzyme, but the L. brevicula enzymes did not. H. discus, H. iris, and O. rusticus enzymes were classified to polysaccharide-lyase family-14 by the analysis of partial amino acid sequences, while the L. brevicula enzymes were not.