灌水对强筋小麦籽粒产量及营养品质的影响

为明确水地强筋冬小麦高产、优质、高效的灌溉技术，试验设3个灌水时期8个灌溉处理［越冬期灌1水（W₁），拔节期灌1水（W₂），孕穗期灌1水（W₃），越冬期和拔节期灌2水（W₁₂），越冬期和孕穗期灌2水（W₁₃），拔节期和孕穗期灌2水（W₂₃），越冬期、拔节期和孕穗期灌3水（W₁₂3），全生育期不灌水处理（CK）］,于小麦成熟期测定籽粒产量、总蛋白及其组分含量和淀粉含量。结果表明，与不灌水的CK比较，所有灌水处理的籽粒产量、有效穗数、穗粒数、千粒重、蛋白质产量以及籽粒淀粉含量均显著增加，但籽粒的总蛋白及其组分含量均呈不同程度降低（W₁处理除外）。越冬期灌水对有效穗数、籽粒产量、总蛋白及其组分含量、淀粉含量的提升作用较大；拔节期灌水对穗粒数的提升作用较大，但对淀粉含量的提升作用较小，对总蛋白及其组分含量的降低作用较大；孕穗期灌水对千粒重的提升作用较大，对蛋白质产量的提升作用较小。随着灌水次数增加，小麦籽粒产量显著提高，淀粉含量先显著提高后基本不变，而籽粒总蛋白及其组分含量降低。W₁₂3处理籽粒产量最高，其次是W₁₃处理；W₁处理籽粒蛋白质及其组分含量最高，其次是W₁₂及W₁₃处理；W₂₃处理淀粉含量最高，其次是W₁₂或W₁₃处理。综合各项指标，最好的灌水组合是越冬期和孕穗期灌2水（W₁₃）。     

不同品种粳稻的锌强化方法研究

通过比较不同锌肥施用方式对不同粳稻品种产量以及稻米锌含量的影响,筛选高效锌水稻品种和最佳锌施用方式。在田间试验条件下,分析9个粳稻品种的稻米产量和锌含量对S(锌肥土施)、SB(锌肥土施结合孕穗期喷施)、SF(锌肥土施结合扬花期喷施)和SBF(锌肥土施结合孕穗期和扬花期喷施)4种锌肥施用方式的响应,结果表明,各水稻品种稻米的锌含量在18.1～29.3 mg·kg~(-1)之间,吉洋1号、吉农大809、吉粳302、吉宏6号、长粳717和稻花香2号为高锌品种,吉农大899为中锌品种,平粳8号和吉粳515为低锌品种。锌肥土施对大多数水稻品种无显著增产作用,不同品种的稻米锌含量在施用锌肥后平均增幅为18.0%;S、SB、SF和SBF处理的稻米锌含量分别较不施锌处理提高了8.3%、17.4%、19.5%和27.0%,但3个喷施处理间的平均锌含量无显著差异。锌肥土施结合叶面喷施能显著提高稻米中的锌含量,不同施用方式的施锌效果因品种而异。选择富锌高产品种,锌肥土施结合适当生育期叶面喷施,可实现增产和稻米锌强化,实现水稻高产优质种植。     

基于网络药理学分析黄芪防控猪繁殖与呼吸综合征的物质基础及靶点信息

为揭示黄芪防控猪繁殖与呼吸综合征(PRRS)的物质基础及靶点信息,采用网络药理学方法,从中药系统药理学数据库与分析平台(TCMSP)筛选黄芪的潜在活性成分、作用靶点,同时从比较毒理基因组学数据库(CTD)收集PRRS相关宿主基因,最后构建"活性成分-关键靶点"网络、蛋白互作网络,并进行GO功能和KEGG通路富集分析。结果显示,从黄芪筛选出的17个潜在活性成分中,有14个潜在活性成分共计65个基因靶点与PRRS相关宿主基因交叉,其中槲皮素、山奈酚、刺芒柄花素、异鼠李素等潜在活性成分可能对治疗PRRS有重要作用,TNF、IL8、TP53、IL6、IL10、IL1B、JUN等45个蛋白靶点间存在相互作用。此外,黄芪治疗PRRS的作用机制可能涉及细胞外间隙和胞浆等组分,并可能与炎症反应、细胞凋亡、T细胞受体信号通路等生物过程相关。本研究为临床应用黄芪及其提取物治疗PRRS奠定了理论基础。     

不同有机肥处理对紫色土油茶林土壤微生物碳源利用的影响

微生物群落碳代谢功能多样性对土壤管理具有重要指示作用,以福建省宁化县紫色土水土侵蚀区油茶人工林不同坡位土壤为研究对象,采用Biolog技术对天然有机物料有机肥(T1)、有机无机复合肥(T2)、禽畜粪便有机(T3)共3种有机肥处理以及不施肥处理(CK)下的土壤微生物碳源利用能力进行了研究。研究结果显示:T1、T2、T3处理下不同坡位土壤的吸光值平均颜色变化率(AWCD)相比于施肥前都有所增加,而CK处理土壤AWCD值无显著变化,不同处理下土壤AWCD值提高的大小顺序表现为T2T1T3CK;Shannon多样性指数、Simpson优势度指数以及McIntosh优势度指数大小顺序均表现为T2T1T3CK;相同处理下不同坡位土壤AWCD值、Shannon多样性指数、Simpson优势度指数以及McIntosh均匀度指数大小顺序总体呈现下坡中坡上坡;Shannon指数与土壤容重和自然含水率呈极显著或显著负相关,与pH值、全碳和全氮含量呈极显著或显著正相关;McIntosh指数与土壤容重、自然含水率、pH值、全碳和全氮含量呈极显著或显著正相关;氨基酸类是各处理后土壤微生物利用的主要碳源类型,主成分分析表明T1、T2、T3处理下土壤微生物对6类碳源利用能力相比于对照具有较大差异,T1和T3处理对于6类碳源的利用具有相似性,T2处理与T3处理之间对于6类碳源利用差异主要在于碳水化合物类碳源。综上,有机无机复合肥的施入更有利于紫色土丘陵区油茶人工林土壤微生物碳源利用能力的提高,以上结论可为制定紫色土丘陵区合理施肥制度的设置、农业优化管理措施提供依据。     

Functional polymorphism among members of abscisic acid receptor family(ZmPYL) in maize

Pyrabactin resistance 1-like proteins(PYLs) are direct receptors of abscisic acid(ABA). For the redundant and polymorphic functions, some members of the PYL family interact with components of other signaling pathways. Here, 253 positive colonies from a maize cDNA library were screened as interacting proteins with the members of ZmPYL family. After sequencing and function annotation, 17 of 28 interaction combinations were verified by yeast two-hybrid(Y2 H). The germination potential, taproot length and proline content of a quartet mutant of Arabidopsis PYL genes were significantly deceased comparing to the wild type(WT) under alkaline stress(pH 8.5) and 100 μmol L–1 methyl jasmonate(MeJA) induction. The malondialdehyde(MDA) content was significantly increased. After germinating in darkness, the characteristics of dark morphogenesis of the quartet mutant seedlings were more obvious than those of the WT. The differential expression of the related genes of photomorphogenesis in the mutant was much more than that in the WT. Three light and two JA responsive cis-affecting elements were identified during the promoter sequences of the AtPYL1 and AtPYL2 genes. These results suggested that functional polymorphism has evolved among the members of ZmPYL family. In response to developmental and environmental stimuli, they not only function as direct ABA receptors but also interact with components of other signaling pathways mediated JA, brassinosteroid(BR), auxin, etc., and even directly regulate downstream stress-related proteins. These signaling pathways can interact at various crosstalk points and different levels of gene expression within a sophisticated network.     

Roles of protein phosphatase 4 in down-regulation of eNOS Ser633 phosphorylation induced by palmitic acid in human umbilical vein endotheli?al cells

AIMTo investigate the roles of protein phosphatase 4 (PP4) in down-regulation of endothelial nitric oxide synthase (eNOS) Ser633 phosphorylation induced by palmitic acid (PA). METHODSHuman umbilical vein endothelial cells (HUVECs) were treated with PA at 25 μmol/L, 50 μmol/L, 100 μmol/L and 200μmol/L for 36 h, or treated with PA at 100 μmol/L for 12 h, 24 h, 36 h and 48 h. Protein phosphatase 2A (PP2A) family inhibitor fostriecin (FST, 20 nmol/L) or okadaic acid (OA, 5 nmol/L) was selected to pretreat the HUVECs for 30 min. Protein phosphatase 4 catalytic subunit (PP4c) siRNA or protein phosphatase 2A catalytic subunit (PP2Ac) siRNA was transfected into the HUVECs. The protein expression levels of of eNOS, PP4c and PP2Ac, as well as the level of eNOS Ser633 phosphorylation, were detected by Western blot. The intracellular nitric oxide (NO) content was measured by DAF-FM DA. RESULTS(1) Compared with control group, the levels of eNOS Ser633 phosphorylation were decreased in PA groups in which the HUVECs were treated with 25 μmol/L, 50 μmol/L, 100 μmol/L and 200 μmol/L PA for 36 h (P<0.05) and 100 μmol/L PA for 24 h, 36 h and 48 h (P<0.05). No significant difference in the level of total eNOS protein expression among all the groups was observed. (2) Compared with control group, both FST and OA pretreatment reversed the reduction of eNOS Ser633 phosphorylation (P<0.05) and the decrease in intracellular NO content (P<0.05) induced by PA. No significant difference in the level of total eNOS protein expression among all the groups was observed. (3) Compared with si-Control group, the PP4c protein expression was significantly reduced (P<0.05), while the level of eNOS Ser633 phosphorylation was significantly increased in si-PP4c group (P<0.05). Although the levels of PP2Ac protein expression declined significantly (P<0.05), the level of eNOS Ser633 phosphorylation remained unchanged in si-PP2Ac group. No significant differencein the level of total eNOS protein expression among all the groups was found. CONCLUSION PA significantly reduces the level of eNOS Ser633 phosphorylation and the content of NO in the HUVECs, which may be due to PA inducing the activation of the PP2A family member PP4 rather than PP2A.     

基于热致液晶弹性体的仿生心脏泵的设计

为设计一款仿生心脏功能较佳的心室泵,采用柔性、热致伸缩的热致形变弹性体代替心肌,根据螺旋心室心肌带理论,选择心肌带的左心室段,并选取了Hilbert平面填充曲线作为热致导体在热致形变弹性体中的走行方式,设计出与真实心脏类似的心室泵结构.通过试验测量了所设计的心室泵的射血分数与心率,结果显示该心室泵的搏出量高于自然心脏,而其心率远低于自然心脏.相对于机械泵,所设计的心室泵结构与真实心脏类似,具有收缩能力强,射血分数高的优点,且不易破坏血细胞,生物相容性较好.不足之处在于,热致动液晶弹性体变形响应慢,暂时还未能达到正常心脏的心率.论证了构建双稳态结构,提高仿生心室泵效率的可能性,以及对于心肌纤维走向较为复杂的其他心肌带段,双轴拉伸机械雕刻对其仿生的可能性.此研究可为容积心脏泵的研发提供新的思路,也可以对右心衰竭等心脏疾病起到辅助治疗的作用.     

Genetic effects of historical anthropogenic disturbance on a long-lived endangered tropical tree Vatica mangachapoi

The endangered Vatica mangachapoi,a longlived,tropical tree with economic and ecological importance found in Hainan,China,was used to assess the hypothesis that historical human activities in Hainan's tropical rain forest could have negative effects on the genetic diversity of V.mangachapoi.Three hundred and twenty individuals from 11 natural populations—which were classified into three groups according to levels of disturbance—were sampled and analyzed with ISSRmarkers.Although genetic diversity of V.mangachapoi is high at the species level,it is relatively low within populations.A significant genetic differentiation occurs among different disturbance levels.Significant isolation-by-distance indicated relevant historical anthropogenic changes.Our findings showed that historical human disturbances significantly increase the genetic differentiation and slightly decrease the genetic diversity of long-lived tree V.mangachapoi.Relevant targeting conservation actions were recommended.     

Use of Microsatellite DNA Profiling to Identify Japanese Flounder,Paralichthys olivaceus of Hatchery Origin

Japanese flounder, Paralichthys olivaceus, is an economically important marine fish species in Asia. A suite of 18 microsatellite markers chosen from published genetic linkage maps was used to carry out parentage assignments of 188 hatchery‐reared juveniles from a small number of breeders. The probabilities of exclusion for the 18 microsatellite markers were 0.604–0.913, and the effectiveness of combined probability of exclusion reached 100% when using the eight microsatellite markers with higher Excl 1 probabilities. The cultured and wild stocks (WSs) were differentiated in a release‐recapture population based on these markers. Of the 321 recaptured offspring, 28.34% were assigned to their parental pairs in our broodstock, whereas the remaining offspring could not be traced back to a possible sire or dam. Significant reduction in genetic diversity of the cultured stock (CS) had not been found compared with that of the WS. The results suggest that CSs released into the wild will not adversely affect the genetic structure of natural populations. Our results demonstrate that these markers provide an efficient tool for parentage assignments and genetic analysis of Japanese flounder.