猕猴桃种质资源保存及育种研究

收集保存猕猴桃属植物３５种或变种、变型,并将它们分为抗寒?喜凉、喜温３种类型。从保存的中华猕猴桃优株中系统选育出“武植２号”、“武植３号”２个优良品种。以中华猕猴桃为母本,毛花猕猴桃为父本进行种间杂交,从杂种Ｆ１代中培养出“江山娇”、“满天星”、“重瓣”３个具有园艺观赏价值的优良株系。这些研究工作为猕猴桃种质资源的保存及新品种的培育奠定了工作基础。     

兰属(Cymbidium)5种植物叶结构特征

采用光学显微镜和体视镜,对兰属5种植物（春兰、蕙兰、建兰、寒兰、墨兰）的叶结构特征（叶脉结构、叶表皮结构、解剖结构）进行了观察和测量。结果显示,兰属5种植物的叶脉结构相似,叶表皮结构和解剖结构存在较大差异,其中最主要的差异是皮下纤维束的多少和边缘角质层锯齿形态。依据叶结构特征聚类分析结果,5种兰可分为春兰组、建兰组和墨兰组3组。本研究表明叶结构特征对兰属5种植物的分类具有重要意义。     

木姜子叶精油的化学成分研究

采用气相色谱-质谱联用仪对产于秦岭太白山的木姜子叶的挥发油成分进行分析鉴定,从分离出的79个峰中鉴定了32种成分,其含量占挥发油总量的90.59％,主要成分为1,3,3-三甲基-乙-氧杂双环[2,2,2]辛烷(59.96％),1,8-桉油醇(8.96％),香茅醛(6.86％),2-甲基-5-(1-甲基乙烯基)环己酮(4.34％)和澄花醇乙酯(3.19％)。     

荧光显微镜观察大蒜油对腹水癌细胞的影响

用吖啶橙染色,荧光显微镜观察大蒜油对—S180,昆明小鼠,U14 C57BL/6J小鼠和L1210DBA小鼠的癌细胞作用的影响,结果表明大蒜油有直接破坏癌细胞的DNA,RNA和分裂中期染色体的作用。给药后2—6小时作用最强,12小时后癌细胞数逐渐恢复,因此给药间隔不应超过12小时。我们研究证实大蒜油有明显的抗癌作用,为临床应用提供有力的依据。     

气候和土地利用变化影响下生态屏障带水土流失趋势研究

受气候和地形等诸多因素影响，我国"两屏三带"国家生态屏障带中的川滇-黄土高原区域和南方丘陵带水土流失十分严重，自然灾害频发。但是，针对川滇-黄土高原区域和南方丘陵带水土流失时空格局变化，特别是未来气候变化和土地利用变化影响下水土流失变化趋势的研究很少。因此，本研究以川滇-黄土高原区域和南方丘陵带为研究对象，利用修正土壤流失方程（RUSLE）定量分析了该区在2000-2015年水土流失的时空变化规律及其影响因素，并预测了在RCP2.6和RCP4.5的未来气候情景下及土地利用变化条件下水土流失的变化趋势。研究结果表明：（1）黄土高原地区在植被恢复的积极作用下，水土流失显著缓解；（2）川滇地区的西南部因植被盖度的增长和降雨的减少水土流失显著缓解，但四川省境内人口密集区农田面积增加以及降水增加造成水土流失大幅度加剧；（3）南方丘陵带受降水增加影响导致了部分区域的水土流失恶化；（4）在未来气候变化情景下，由于大部分地区降雨将减少使土壤侵蚀趋于缓解，但四川、黄土高原和南方丘陵带大部分地区仍然面临未来农田面积增加带来的水土侵蚀压力。考虑到未来气候变化情景下降雨减少的趋势，建议在黄土高原地区提高草地在土地利用类型中的占比，在减少耗水量的同时维持地表盖度，缓解水土侵蚀；此外，各区域仍需控制农田面积，而且需通过加强坡耕地上保水保土耕作措施降低农田区域的土壤侵蚀压力。     

Engineering the Saccharomyces cerevisiae β-Oxidation Pathway to Increase Medium Chain Fatty Acid Production as Potential Biofuel

Fatty acid-derived biofuels and biochemicals can be produced in microbes using β-oxidation pathway engineering. In this study, the β-oxidation pathway of Saccharomyces cerevisiae was engineered to accumulate a higher ratio of medium chain fatty acids (MCFAs) when cells were grown on fatty acid-rich feedstock. For this purpose, the haploid deletion strain Δpox1 was obtained, in which the sole acyl-CoA oxidase encoded by POX1 was deleted. Next, the POX2 gene from Yarrowia lipolytica, which encodes an acyl-CoA oxidase with a preference for long chain acyl-CoAs, was expressed in the Δpox1 strain. The resulting Δpox1 [pox2+] strain exhibited a growth defect because the β-oxidation pathway was blocked in peroxisomes. To unblock the β-oxidation pathway, the gene CROT, which encodes carnitine O-octanoyltransferase, was expressed in the Δpox1 [pox2+] strain to transport the accumulated medium chain acyl-coAs out of the peroxisomes. The obtained Δpox1 [pox2+, crot+] strain grew at a normal rate. The effect of these genetic modifications on fatty acid accumulation and profile was investigated when the strains were grown on oleic acids-containing medium. It was determined that the engineered strains Δpox1 [pox2+] and Δpox1 [pox2+, crot+] had increased fatty acid accumulation and an increased ratio of MCFAs. Compared to the wild-type (WT) strain, the total fatty acid production of the strains Δpox1 [pox2+] and Δpox1 [pox2+, crot+] were increased 29.5% and 15.6%, respectively. The intracellular level of MCFAs in Δpox1 [pox2+] and Δpox1 [pox2+, crot+] increased 2.26- and 1.87-fold compared to the WT strain, respectively. In addition, MCFAs in the culture medium increased 3.29-fold and 3.34-fold compared to the WT strain. These results suggested that fatty acids with an increased MCFAs ratio accumulate in the engineered strains with a modified β-oxidation pathway. Our approach exhibits great potential for transforming low value fatty acid-rich feedstock into high value fatty acid-derived products.     

iTRAQ‐Based Proteomics Reveals that the Tomato ms1035 Gene Causes Male Sterility through Compromising Fat Acid Metabolism

So far, over 50 spontaneous male sterile mutants of tomato have been described and most of them are categorized as genetic male sterility. To date, the mechanism of tomato genetic male sterility remained unclear. In this study, differential proteomic analysis is performed between genetic male sterile line (2‐517), which carries the male sterility (ms10³⁵) gene, and its wild‐type (VF‐11) using isobaric tags for relative and absolute quantification‐based strategy. A total of 8272 proteins are quantified in the 2–517 and VF‐11 lines at the floral bud and florescence stages. These proteins are involved in different cellular and metabolic processes, which express obvious functional tendencies toward the hydroxylation of the ω‐carbon in fatty acids, the tricarboxylic acid cycle, the glycolytic, and pentose phosphate pathways. Based on the results, a protein network explaining the mechanisms of tomato genetic male sterility is proposed, finding the compromising fat acid metabolism may cause the male sterility. These results are confirmed by parallel reaction monitoring, quantitative Real‐time PCR (qRT‐PCR), and physiological assays. Taken together, these results provide new insights into the metabolic pathway of anther abortion induced by ms10³⁵ and offer useful clues to identify the crucial proteins involved in genetic male sterility in tomato.