不同杀青方式龙井茶自动化连续生产线加工工艺探讨

文章剖析了不同杀青方式龙井茶自动化连续生产线的设备配置和工艺流程,对生产线的龙井茶品质进行感官评价,为龙井茶生产线推广应用提供借鉴。     

掌叶覆盆子种子繁殖力关键影响因素分析

掌叶覆盆子野外种群的更新由根蘖繁殖完成,实生苗罕见,种子繁殖力低。本研究从掌叶覆盆子种子的结实特性、采种期、储藏时间、母树来源、激素含量变化与种子萌发等方面对其种子繁殖力影响因素进行了全面的分析。结果表明:掌叶覆盆子种子数量充足,群体内结实特性保持着一致性;当年熟果种子活力达到75.33%,储藏时间超过1年种子活力迅速下降且发芽率为0;不同母树来源种子发芽率无差异;青果、黄绿果时期种子活力和发芽率都较低,熟果和过熟果实种子活力达最高值且基本一致,但熟果GA 3/ABA比值最大,发芽率最高;不管是否添加外源激素,随着果实过熟程度加深,种子发芽率迅速下降,种子休眠程度也随之加深;酸蚀和激素可有效破除休眠,提高发芽率。采种时间、储藏时间、酸蚀和赤霉素催芽等是影响掌叶覆盆子繁殖力的关键因素。     

灰绿碱蓬多糖脱蛋白工艺研究

蛋白本身具有热敏感性,糖蛋白复合物在脱除蛋白质以后,多糖自身的生物活性会明显增加。本文测定了灰绿碱蓬根、茎、叶的基本营养成分,采用水提醇沉法提取了灰绿碱蓬多糖,并优化了多糖脱蛋白工艺比较了Savage法、(NH4)SO4沉淀法、TCA法和酶-Savage法这4种方法的脱蛋白效果。结果显示,灰绿碱蓬多糖的最佳脱蛋白方式为酶-Savage法,酶添加量为7%,Savage溶液处理一次,此条件下脱蛋白效果和多糖保留率均最好,蛋白质脱除率为80.71%,多糖保留率为67.27%。     

MicroRNA-145 inhibits epithelial-mesenchymal transition in human renal cancer A-498 cells by ADAM28

AIM: To investigate the inhibitory effect of microRNA-145 (miR-145) on epithelial-mesenchymal transition (EMT) in renal cancer A-498 cells. METHODS: The A-498 cells were transfected with miR-145 mimics (M145) and mimic negative control(MNC), which served as M145 group and MNC group, respectively. Mock control (MC) group was set up using untreated A-498 cells. The expression level of miR-145 in each group was detected by RT-qPCR. Transwell assay was used to detect the invasion ability of the cells. The protein expression of vimentin, E-cadherin and ADAM28 was determined by Western blot. Bioinformatic method was used to predict the target genes of miR-145. Antagonistic effect of ADAM28 over-expression on the inhibition of EMT by miR-145 was detected by Western blot. The relationship between miR-145 and ADAM28 was analyzed by dual-luciferase reporter assay. RESULTS: The expression level of miR-145 in M145 group was significantly up-regulated than that in MC group (P<0.05). The number of invasive cells in M145 group was 12.78±3.37, which was significantly lower than that in MC group (P<0.05). ADAM28 may be the target gene of miR-145. Compared with MC group, the protein expression of vimentin and ADAM28 in M145 group was significantly decreased (P<0.05), while the protein expression of E-cadherin was significantly increased (P<0.05).After ADAM28 over-expression, the protein expression of vimentin in the A-498 cells of M145 group was significantly increased (P<0.05), and the protein expression of E-cadherin was significantly decreased (P<0.05). The results of dual-lucife-irasei reporter assay showed that ADAM28 was a downstream target gene of miR-145. CONCLUSION: miR-145 may inhibit the expression of EMT-related proteins through the downstream target gene ADAM28 and inhibit the EMT process of renal cancer A-498 cells.     

miR-140-3p inhibits viability,invasion and migration of non-small-cell lung cancer A549 cells by targeting PD-L1

AIM: To explore the target relationship between microRNA-140-3p (miR-140-3p) and programmed cell death ligand 1 (PD-L1) and their effect on the viability, migration and invasion of non-small-cell lung cancer A549 cells.METHODS: RT-qPCR was used to detect the miR-140-3p expression in HLF-1, A549 and H1299 cells, and then the A549 cells with the most significant difference were selected as the subsequent research object. TargetScan software and dual-luciferase reporter assay were performed to predict and confirm the target relationship between miR-140-3p and PD-L1. RT-qPCR and Western blot were used to determine the effects of miR-140-3p mimic and inhibitor on PD-L1 expression level. MTT assay was used to detect the viability of A549 cells. Transwell assay was performed to detect the migration and invasion abilities of the A549 cells.RESULTS: miR-140-3p was significantly down-regulated in the A549 cells and H1299 cells (P<0.05). Transfection with miR-140-3p mimic decreased the expression of PD-L1 and inhibited the viability, migration and invasion of the A549 cells. Transfection with pcDNA3.0-PD-L1 reversed the inhibitory effect of miR-140-3p on the viability, migration and invasion of the A549 cells.CONCLUSION: miR-140-3p inhibits the viability, migration and invasion of A549 cells by targeting PD-L1.     

Effect of dietary calcium or phosphorus deficiency on bone development and related calcium or phosphorus metabolic utilization parameters of broilers from 22 to 42 days of age

This experiment was conducted to investigate the effect of dietary calcium (Ca) or phosphorus (P) deficiency on bone development and related Ca or P metabolic utilization parameters of broilers from 22 to 42 days of age based on our previous study, which indicated that dietary Ca or P deficiency impaired the bone development by regulating related Ca or P metabolic utilization parameters of broilers from 1 to 21 days of age. A total of 504 one-day-old Arbor Acres male broilers were randomly assigned to 1 of 4 treatments with 7 replicates in a completely randomized design, and fed the normal control and Ca- or P-deficient diets from 1 to 21 days of age. At 22 days of age, the broilers were further fed the normal control diet (0.90% Ca+0.35% non-phytate P (NPP)), the P-deficient diet (0.90% Ca+0.18% NPP), the Ca-deficient diet (0.30% Ca+0.35% NPP) or the Ca and P-deficient diet (0.30% Ca+0.18% NPP), respectively. The results showed that dietary Ca or P deficiency decreased (P<0.05) tibia bone mineral density (BMD), bone breaking strength (BBS), ash content, tibia ash Ca content and serum P content on days 28 and 42, but increased (P<0.05) tibia alkaline phosphatase (ALP) activity of broilers on day 42 compared with the control group. Furthermore, the broilers fed the P-deficient diet had the lowest (P<0.05) tibia BMD, BBS, ash content, serum P content and the highest (P<0.05) serum Ca content on day 28 compared with those fed the Ca-deficient or Ca and P-deficient diets. The results from the present study indicated that the bone development and related Ca or P metabolic utilization parameters of broilers were the most sensitive to dietary P deficiency, followed by dietary Ca deficiency or Ca and P-deficiency; dietary Ca or P deficiency impaired the bone development possibly by regulating serum Ca and P contents as well as tibia Ca content and ALP activity of broilers from 22 to 42 days of age.     

壮秧影响不同节氮水平下早稻产量及氮肥吸收利用

【目的】培育壮秧和施用分蘖肥是促进水稻早发的重要措施,但增施分蘖肥易导致水稻无效分蘖增加和氮素流失。研究双季稻区早稻壮秧和分蘖肥节氮条件下产量形成和氮素吸收利用特性,以期为早稻节氮控污和丰产栽培提供科学依据。【方法】以超级杂交早稻‘淦鑫203’为材料,采用壮苗育秧(状秧)和普通育秧(普秧)两种方式培育秧苗。于2014-2015年进行大田试验,设置壮秧常规施氮(VS+100%N)、节氮10%(VS–10%N)、节氮20%(VS–20%N)、节氮30%(VS–30%N) 4个处理,以普秧常规施氮(NS+100%N)处理和不施氮空白(NS+0N)处理分别作对照,共6个处理。减施的氮肥均在分蘖肥中扣除,除不施氮对照外,各处理基肥氮(72 kg/hm^2)和穗肥氮(54 kg/hm^2)均保持不变。分析早稻拔节期、齐穗期和成熟期SPAD值、光合速率、硝酸还原酶活性和各器官氮素含量,并测定成熟期水稻产量及其构成,明确了植株总氮积累量、氮素转运量、氮表观转运率、氮素利用效率等。【结果】与NS+100%N处理相比,壮秧条件下分蘖肥节氮10%~30%对叶片SPAD值和光合速率无显著影响,但壮秧能促进分蘖发生和成穗,在生育中后期可逐渐弥补分蘖肥节氮对分蘖期干物质积累的不利影响,成熟期VS–10%N和VS–20%N处理干物质积累量较对照NS+100%N增加,产量分别增加了8.5%和1.5%;VS–30%N处理干物质积累量和产量则呈下降趋势。同时,壮秧有利于提高早稻叶片硝酸还原酶活性、各器官氮含量和氮积累量,与NS+100%N处理相比,VS+100%N处理成熟期氮素积累量显著增加了6.9%,VS–10%N和VS–20%N处理无显著变化,VS–30%N处理显著下降了9.7%。壮秧处理氮素回收率和氮素农学效率较NS+100%N处理分别显著提高了12.1%~22.4%和9.9%~24.7%(P <0.05)。【结论】双季稻区早稻壮秧可以促进分蘖早发,提高叶片的干物质生产能力和氮代谢性能,弥补分蘖肥减氮后对水稻前期生长的不利影响,提高后期的干物质生产量和氮运转量。通过培育壮秧,分蘖肥减施总施氮量的20%以内,早稻产量不会下降,可实现水稻的节氮、丰产和节本栽培,有利于提高氮素利用效率和减少氮素流失对环境的污染。     

林地开垦对黄土区坡面土壤养分空间分布的影响

研究黄土高原侵蚀环境下林地开垦后坡面土壤养分空间分布状况,确立林地开垦后侵蚀驱动的坡地土壤养分空间变异特征。以黄土高原丘陵区子午岭林地和开垦28年的侵蚀坡面为研究对象,分析土壤主要性质和养分含量的变化情况,运用经典统计学和地统计法分析坡面土壤基本性质和养分空间分布规律。林地开垦后坡面土壤pH增加了0.24个单位,有机质、全氮、全磷和铵态氮、硝态氮、速效磷和速效钾分别降低了13.77,1.14,0.10 g/kg和6.05,1.63,4.99,58.44 mg/kg。林地的土壤有机质、全氮和全磷的变异系数大于开垦地,而pH和各速效养分的变异系数小于开垦地。开垦后中坡位和下坡位养分含量减少幅度较大,上坡位减少幅度较小。林地和开垦地的土壤各指标都呈中等或强烈的空间自相关。林地开垦增强了有机质、全氮、全磷、铵态氮、速效磷和速效钾的空间异质性,但减小了pH的空间异质性,地形等结构性因子主导了土壤养分空间异质性的形成。林地开垦后,pH、有机质、全氮和全磷变程增大,铵态氮、硝态氮和速效钾变程减小,速效磷在2个坡面上的变化趋势不一致。研究结果表明林地开垦极大地减少了坡面土壤养分含量,但减少幅度与坡位和坡面形态有关。同时,开垦增大了坡面土壤有机质、全氮和全磷的空间依赖性,减小了速效养分的空间依赖性。     

青花椒采收机环切式穗枝分离装置设计与试验

青花椒采收过程中，果皮上散生多数突起的油苞极易破裂导致果实干后变黑，有效成分挥发而严重影响质量。青花椒的油苞破损程度直接影响其品质，在保证花椒低油苞破损率的前提下，为实现花椒机械化采收，基于枝条环切原理，设计了一种花椒采收机的穗枝分离装置。通过理论分析得到影响采收效果的结构参数和作业参数，并根据花椒枝条物理特性和加工经济性进行优化。选取环切式穗枝分离装置的环切刀刃口角度、环切刀转速和枝条进给速度为试验因素，以花椒采收效率和油苞破损率作为评价指标，进行了单因素试验及二次正交旋转组合试验。采用响应曲面法对试验结果进行分析并找出主控因素，运用Design-Expert软件的多目标优化算法进行参数优化。结果表明，枝条进给速度是影响花椒采收效率和油苞破损率的主要因素，枝条进给速度与花椒采收效率成正比关系。各因素对花椒采收效率和油苞破损率的影响程度由大到小依次为枝条进给速度＞环切刀转速＞环切刀刃口角度。随着枝条进给速度的增加，花椒采收效率迅速提高，花椒油苞破损率先缓慢增加后急剧增加。随着环切刀转速的增加，花椒采收效率并无明显增加，在枝条进给速度＜0.4 m/s时，花椒油苞破损率随环切刀转速增加先小幅减小后趋于平稳最后小幅增加，在枝条进给速度＞0.4 m/s时，花椒油苞破损率随环切刀转速增加平稳减小。该装置最优参数组合:环切刀转速2 800 r/min，枝条进给速度0.45 m/s，环切刀刃口角度25°。样机田间试验表明，花椒采收效率和油苞破损率分别为50.7 kg/h和6.7%，优于目前人工采摘作业效果。      

Effects of platelet-rich plasma on chondrocyte apoptosis and NLRP3/IL-1β signaling pathway in rabbits with osteoarthritis

AIM To explore the effect of platelet-rich plasma (PRP) on rabbit osteoarthritis and its possible mechanism. METHODS The rabbits with knee osteoarthritis were prepared and then divided into model group, sodium hyaluronate (SH) group and PRP group, and another sham operation group was set up, with 6 rabbits in each group. The gross morphological changes of rabbit cartilage were observed. HE staining was used to evaluate the pathomorphological changes of the cartilage. TUNEL staining was used to detect the apoptosis of chondrocytes. The expression of nucleotide-binding oligomerization domain-like receptor protein 3 (NLRP3)/interleukin-1β （IL-1β） signaling pathway-related molecules was observed by immunohistochemical staining, and the protein levels of caspase-3, Bcl-2 and Bax were determined by Western blot. Chondrocytes were isolated and processed according to grouping, and the NLRP3 and IL-1β levels of the cells were measured by ELISA. RESULTS Compared with sham operation group, Pelletier score, Mankin score, chondrocyte apoptotic rate, the positive protein expression rates of NLRP3, apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), caspase-1 and IL-1β, and the protein levels of caspase-3 and Bax in model group were increased significantly (P<0.05), while the protein expression of Bcl-2 was decreased significantly (P<0.05). Compared with model group, Pelletier score, Mankin score, the apoptotic rate of chondrocytes, the positive protein expression rates of NLRP3, ASC, caspase-1 and IL-1β, and the protein levels of caspase-3 and Bax in SH group and PRP group were decreased significantly (P<0.05), while the protein expression of Bcl-2 was increased significantly (P<0.05). In PRP group, Pelletier score, Mankin score, the apoptotic rate of chondrocytes, the positive protein expression rates of NLRP3, ASC, caspase-1 and IL-1β, and the protein levels of caspase-3 and Bax were lower than those in SH group, while the protein expression of Bcl-2 was higher than that in SH group (P<0.05). Compared with control group, the expression of NL?RP3 and IL-1β in MCC950 (NLRP3 ihibitor) group were significantly reduced (P<0.05), the expression of NLRP3 in eucalyptol (IL-1β inhibitor) group was not significantly changed (P>0.05), and the expression of IL-1β was significantly reduced (P<0.05). CONCLUSION Platelet-rich plasma promotes the repair of cartilage in osteoarthritis rabbits, which has better effect than SH. The mechanism may be related to the inhibition of NLRP3/IL-1β pathway and the reduction of chondrocyte apoptosis.