干旱胁迫下外源油菜素内酯对玉米幼苗光合作用和D1蛋白的调控效应

为了揭示干旱胁迫下外源油菜素内酯对玉米幼苗光合作用的保护机制,采用溶液培养的方法,以驻玉309为试验材料,研究外源油菜素内酯(BR)预处理及20% PEG-6000模拟干旱胁迫后玉米幼苗的生长参数、叶绿素含量、光合参数、叶绿素荧光参数及D1蛋白含量的变化。结果表明,与干旱胁迫处理(PEG)相比,BR+PEG处理的玉米苗株高增加45.87%,根长增加20.56%,总干物质积累增加8.01%,叶片相对含水量提高4.50%,叶绿素a含量增加26.32%,光合参数(Pn、Gs、Ci、Tr)分别提高9.57%,38.23%,30.19%,28.12%,光合系统Ⅱ(ΦPSⅡ)活性提高了20.48%,最大光化学效率提高了0.66%,光合系统Ⅱ绝对电子传递速率(ETR(Ⅱ)和相对电子传递速率r ETR(Ⅱ))分别提高20.40%和31.02%;D1蛋白含量增加37.34%(P0.05)。说明在干旱胁迫条件下叶片喷施BR可以改善玉米幼苗的生长发育,减缓光合系统的损伤,促进D1蛋白质的稳定,从而提高玉米幼苗对干旱胁迫的适应性。     

吉林延龄草种子内源抑制物质初步研究

为探讨吉林延龄草种子内源抑制物质生理活性及种子中抑制物质的去除方法,采用乙酸乙酯、甲醇、水提取吉林延龄草种子并测定其提取物对白菜、水稻幼苗生长的抑制活性,用温水(25,35,45℃)浸种并测定各批次浸提液抑制活性,结果表明,吉林延龄草种子浸提液(乙酸乙酯提取液除外)对白菜幼根及胚轴,水稻幼根均有显著抑制作用,且抑制物质的活性随着提取物浓度的增加而增强,吉林延龄草种子水提取液(C)对白菜和水稻幼苗生长的抑制活性高于甲醇提取液(B)的生物活性,吉林延龄草种子乙酸乙酯提取液对白菜和水稻幼苗无显著抑制作用(p＞0.05),吉林延龄草种子经乙酸乙酯、甲醇溶液提取后,再经蒸馏水提取获得的水提液Ⅱ(E)对白菜和水稻幼苗生长的抑制活性减弱;温水浸泡可将其内源抑制物质浸提出来,且随着浸种时间的增加,浸提液对白菜幼根及胚轴的抑制作用呈现先增加而后逐渐降低的趋势.25℃蒸馏水浸泡种子第5天浸提液抑制作用达到最大,对白菜幼根及胚轴的抑制作用分别达到65.89％和25.69％,35℃蒸馏水浸泡种子第3天浸提液抑制作用达到最大,对白菜幼根及胚轴的抑制作用分别达到82.14％和59.93％,45℃蒸馏水浸泡种子第2天浸提液抑制作用达到最大,对白菜幼根及胚轴的抑制作用分别达到90.62％和83.86％.综合分析表明,吉林延龄草种子中存在活性较高的内源抑制物,用45℃温水浸泡可有效除去种子内源抑制物质.     

云南省荞麦叶枯病病原菌鉴定及其生物学特性

为明确云南省荞麦叶枯病病原菌种类,采用常规组织分离法获得病原菌菌株LW2015.3,通过形态学特征及分子生物学技术对菌株LW2015.3进行鉴定,并研究其生物学特性。结果表明,荞麦叶枯病病原菌的分生孢子呈倒棍棒状或倒梨状,褐色,具3～8个横隔膜,0～4个纵斜隔膜,大小为16.5～45.0μm×5.0～13.5μm,厚垣孢子呈球形,直径为6.0～12.0μm;该菌株ITS序列系统发育进化分析结果表明,菌株LW2015.3与链格孢Alternaria alternata(登录号:MG195995.1)的同源性为100%,结合形态学特征与分子鉴定结果确定云南省荞麦叶枯病病原菌为链格孢A. alternata(登录号:KT362732.1)。该病原菌菌丝生长适宜温度为20～30℃,25℃为最适温度;当p H为6～9时菌丝生长速率加快,pH 7最适菌丝生长;PDA培养基和PSA培养基最适菌丝生长;该病原菌对以麦芽糖为碳源和以硝酸钠为氮源时的利用率最高;菌丝的致死温度为50℃,10 min;不同光照条件对菌丝生长的影响有显著差异,连续光照最有利于菌丝生长。     

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.     

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.     

淮安市食品产业转型升级与高职教育发展关联研究

高职教育发展影响着着区域产业的发展,区域产业的发展又决定着对高职人才的需求.文章运用教育学和产业经济学有关理论,探讨淮安食品产业发展存在的问题和淮安市食品大类高职教育现状,基于两者紧密关联的角度,从政府、学校、企业三个维度,共提出了八条针对性措施.     

基于稳定同位素特征与土壤性质的有机茶身份辨识研究

为探究云南普洱地区有机茶身份辨识特征,完善高原有机茶身份辨识技术,选取云南省普洱市的5个代表性有机种植认证茶园（ZX、LS、CYT、YS、HL）和相邻的5个常规茶园（C-1、C-2、C-3、C-4、C-5）,采集300余份茶叶和土壤样本,结合稳定同位素比例质谱仪、元素分析仪等测定茶叶和土壤的δ¹⁵N丰度、δ¹³C丰度、全氮、全碳、有机碳、碱解氮等指标,通过因子分析和判别分析的方法构建了有机茶叶同位素-土壤性质判别模型,并使用Holdout法进行验证。结果表明：不同茶园有机茶叶与相邻常规茶叶相比未表现出一致的δ¹⁵N,δ¹³C值差异规律,因此,使用单一稳定同位素因子难以鉴别有机茶。通过进一步对茶叶和土壤性质进行因子分析,筛选出6个适合判别的特征向量,构建了基于同位素特征和土壤性质的多元有机判别模型,其判别函数方程为：y=-0.081（茶叶δ¹⁵N）＋0.819（茶叶δ¹³C）＋0.093（土壤全氮）＋2.117（土壤全碳）－0.155（土壤有机碳）＋2.870（土壤pH）＋4.232,y<0.5为常规茶,判别准确度为92.3%。综上,基于同位素特征值和土壤性质参数指标构建的多元有机判别模型可实现云南省普洱市高原有机茶身份的准确判别。     

碳交易视域下养殖户畜禽粪污资源化利用受偿意愿与影响因素——基于河北省7市694户养猪户调研数据

为进一步探究养殖户粪污资源化利用受偿意愿、受偿水平及其影响因素,基于碳交易视角,利用2023年3—4月对河北省7市694户养猪户的调研数据,运用条件价值评估法、二元Logit模型和Tobit模型对此进行系统分析。结果表明：1）88.76%的养猪户愿意接受补偿,其受偿水平在25.03~31.50元/t;2）养猪户年龄、养殖场地面积以及粪污资源化利用生态效益等因素会显著影响养猪户受偿意愿;风险偏好、场地面积、养殖规模、养殖信息获取渠道、粪污资源化利用经济效益显著影响其受偿水平;3）规模异质性视角下,粪污资源化利用生态效益显著正向影响不同规模养猪户受偿意愿。自动化设施配置数量和粪污资源化利用社会效益显著影响不同规模养猪户受偿水平,但其影响方向存在显著差异。为使养殖户更好参与资源化利用,应加强对畜禽粪污资源化利用正面效果的宣传,将宏观政策规范与地方实际相结合、因地制宜,有序推进碳交易补偿机制的建立。