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学者姓名：申宝营
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Abstract ：
Low temperature, weak light, and the combination of low temperature and weak light can have an impact on the growth, development, and quality of eggplants. The color of the eggplant peel is affected by the anthocyanin content. To better understand the influence of low temperature, weak light, and the combination of low temperature and weak light on the regulation of anthocyanins in the eggplant peel, four treatments were carried out on the eggplants, respectively: low temperature (18/13 degrees C, 250 mu mol/(m2s)), weak light intensity (WL, 25/20 degrees C, 120 mu mol/(m2s)), low temperature combined with weak light intensity (LW, 18/13 degrees C, 120 mu mol/(m2s)), and the control (CK, 25/20 degrees C, 250 mu mol/(m2s)). The effects of low temperature and weak light on the anthocyanin content in various parts of the eggplant were analyzed, and transcriptome analysis was performed on the eggplant peel under the treatments of low temperature, weak light, and the combination of low temperature and weak light using RNA sequencing. The anthocyanin content in eggplants increased under low temperature and the combination of low temperature and weak light treatments, while it decreased under weak light. KEGG analysis showed that three pathways, namely phenylpropanoid biosynthesis, flavonoid biosynthesis, and anthocyanin biosynthesis, were involved in the anthocyanin biosynthesis of eggplants. Pearson correlation coefficients indicated that the anthocyanin content in the eggplant peel under low temperature and the combination of low-temperature and weak-light treatments was significantly correlated with SmPAL, Sm4CL, SmCYP73A100, SmCHS, SmCHI, F3H, DFR, ANS, and 3GT, and also significantly correlated with MYB, bHLH, and AP2/ERF. Under low-temperature and the combination of low-temperature and weak-light stress, the anthocyanin content increased due to the significant down-regulation of 3GT.
Keyword ：
anthocyanin anthocyanin eggplant (Solanum melongena L.) eggplant (Solanum melongena L.) transcription factor transcription factor transcriptome transcriptome
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| GB/T 7714 | Shen, Baoying , Wu, Hongqi , Xie, Xinxin et al. Comparative Transcriptomic Analyses of Anthocyanin Biosynthesis Genes in Eggplant Under Low Temperature and Weak Light [J]. | PLANTS-BASEL , 2025 , 14 (3) . |
| MLA | Shen, Baoying et al. "Comparative Transcriptomic Analyses of Anthocyanin Biosynthesis Genes in Eggplant Under Low Temperature and Weak Light" . | PLANTS-BASEL 14 . 3 (2025) . |
| APA | Shen, Baoying , Wu, Hongqi , Xie, Xinxin , Zhao, Bo , Chen, Peiqiang , Ao, Deyong et al. Comparative Transcriptomic Analyses of Anthocyanin Biosynthesis Genes in Eggplant Under Low Temperature and Weak Light . | PLANTS-BASEL , 2025 , 14 (3) . |
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[目的]探究外源葡萄糖对黄瓜嫁接苗生长发育及光合特性的影响，为其嫁接技术体系的优化提供参考。[方法]以‘壮士’南瓜为砧木，‘中农26号’黄瓜为接穗，采用改良版顶插固定嫁接法进行嫁接。在嫁接愈合期分别喷施13.9、27.8、41.7、55.6 mmol·L
Keyword ：
光合特性 光合特性 外源葡萄糖 外源葡萄糖 嫁接 嫁接 生长发育 生长发育 黄瓜 黄瓜
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| GB/T 7714 | 毕格 , 黄晓东 , 申宝营 et al. 外源葡萄糖对黄瓜嫁接苗生长及光合特性的影响 [J]. | 亚热带农业研究 , 2025 , 21 (02) : 125-135 . |
| MLA | 毕格 et al. "外源葡萄糖对黄瓜嫁接苗生长及光合特性的影响" . | 亚热带农业研究 21 . 02 (2025) : 125-135 . |
| APA | 毕格 , 黄晓东 , 申宝营 , 焦玉兰 , 林碧英 , 郑秀玉 . 外源葡萄糖对黄瓜嫁接苗生长及光合特性的影响 . | 亚热带农业研究 , 2025 , 21 (02) , 125-135 . |
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Pectin methylesterases (PMEs) and their inhibitors (PMEIs) serve as pivotal enzymes in pectin methylation modifications, playing crucial roles in plant morphogenesis, cell adhesion, and maintenance of the cell wall integrity. However, there have been limited studies exploring the functions of the PME/PMEI gene families in the healing process of grafted-cucumber seedlings and their responses to stress conditions. In this study, we identified 52 CsaPME family members and 33 CsaPMEI family members as well as 86 CmoPME family members and 36 CmoPMEI family members. Comprehensive analyses of the PME/PMEI gene families in cucumber and pumpkin were conducted using bioinformatics techniques. Additionally, the PME/PMEI gene families in cucumber and pumpkin exhibited distinct expression modes in different vegetative organs of homologous/heterologous-grafted seedlings and under chilling stress. Notably, the cucumber/pumpkin-grafted seedlings exhibited responses in the roots and leaves involving PMEI and type I proPME genes, facilitating their adaptation to chilling stress. Additionally, an investigation into the responsiveness of cucumber/pumpkin-grafted seedlings during the healing phase to varying light intensity modes revealed that the implementation of a higher light intensity mode resulted in an upregulation of the expression levels of the majority of PME/PMEI family genes, particularly those belonging to the PME family, during the critical stages of isolation layer and callus formation. Based on these findings, six key PME/PMEI family members responsive to different light intensity modes during graft healing were selected. Through the prediction of transcription factor binding sites and an analysis of the response to different light intensity modes during graft healing, four Dof transcription factors with potential regulatory relationships with these six key PME/PMEI genes were identified. This suggests that cucumber/pumpkin-grafted seedlings can regulate key PME/PMEI genes via Dof factors in response to different light intensity modes during the healing process, thereby influencing the progression of graft healing.
Keyword ：
cucumber cucumber graft healing graft healing light intensity mode light intensity mode PME/PMEI gene family PME/PMEI gene family pumpkin pumpkin
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| GB/T 7714 | Lin, Huangfang , Ye, Huilan , Shao, Qingqing et al. Genome-Wide Analyses and Expression Profiling of PME/PMEI Gene Families Reveal Their Relevance to Chilling Stress Response and Grafted Healing Efficiency in Cucumber/Pumpkin-Grafted Plants [J]. | PLANTS-BASEL , 2025 , 14 (9) . |
| MLA | Lin, Huangfang et al. "Genome-Wide Analyses and Expression Profiling of PME/PMEI Gene Families Reveal Their Relevance to Chilling Stress Response and Grafted Healing Efficiency in Cucumber/Pumpkin-Grafted Plants" . | PLANTS-BASEL 14 . 9 (2025) . |
| APA | Lin, Huangfang , Ye, Huilan , Shao, Qingqing , Cheng, Saichuan , Bi, Ge , Lin, Biying et al. Genome-Wide Analyses and Expression Profiling of PME/PMEI Gene Families Reveal Their Relevance to Chilling Stress Response and Grafted Healing Efficiency in Cucumber/Pumpkin-Grafted Plants . | PLANTS-BASEL , 2025 , 14 (9) . |
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为研究芸苔素内酯对黄瓜幼苗耐旱性的影响，以黄瓜品种中农106号为试验材料，在黄瓜生长第8天(1叶1心期)后分别喷施0.00、0.05、0.10、0.20μmol/L的2,8-表高芸苔素内酯溶液后进行干旱胁迫，同时以等量清水喷施的不干旱处理作为对照。断水48 h后恢复浇水使其继续生长，5 d后对黄瓜幼苗的生长量、抗氧化体系、渗透调节物质、过氧化物、叶绿素荧光参数等指标进行测定。结果表明，与未喷施芸苔素内酯处理组相比，叶面喷施芸苔素内酯可以有效缓解黄瓜叶片光合系统损伤，提高黄瓜叶片中的SOD保护酶活性和脯氨酸的含量，同时减少丙二醛的累积，进而减轻黄瓜幼苗在干旱胁迫下受到的损害，有效促进黄瓜幼苗下胚轴长、株高、茎粗、叶面积、根长度、根表面积、植株鲜重和光合能力等多项指标的增长，有利于干旱胁迫后黄瓜幼苗的恢复生长，增强黄瓜幼苗的抗旱能力。其中以0.10μmol/L芸苔素内酯稀释液喷施叶片，对促进黄瓜幼苗干旱胁迫后恢复生长的综合效果最好，其光合能力最优，SOD活性较0.00μmol/L约提高3.41%,脯氨酸含量较0.00μmol/L约提高9.36%,丙二醛含量较0.00μmol/L约降低43.20%。综上表明，芸苔素内酯喷施可减轻黄瓜幼苗在干旱胁迫下受到的损害，提升黄瓜幼苗耐旱性。
Keyword ：
光合作用 光合作用 干旱胁迫 干旱胁迫 生长量 生长量 芸苔素内酯 芸苔素内酯 黄瓜 黄瓜
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| GB/T 7714 | 胡永波 , 雷雨田 , 杨永森 et al. 芸苔素内酯喷施对黄瓜幼苗耐旱性的影响 [J]. | 江苏农业科学 , 2024 , 52 (09) : 195-203 . |
| MLA | 胡永波 et al. "芸苔素内酯喷施对黄瓜幼苗耐旱性的影响" . | 江苏农业科学 52 . 09 (2024) : 195-203 . |
| APA | 胡永波 , 雷雨田 , 杨永森 , 罗楚渺 , 申宝营 . 芸苔素内酯喷施对黄瓜幼苗耐旱性的影响 . | 江苏农业科学 , 2024 , 52 (09) , 195-203 . |
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【目的】探究低温、弱光、低温弱光处理对茄子幼苗期、花期、果期花青素含量的影响，以及对茄子品质的影响，为茄子的优质培育以及高产栽培奠定理论基础。【方法】以紫黑茄秀娘为试验材料，分别在幼苗期、花期、果期进行低温（18℃/13℃，250μmol·m~(-2)·s~(-1)）、弱光（25℃/20℃，120μmol·m~(-2)·s~(-1)）、低温弱光（18℃/13℃，120μmol·m~(-2)·s~(-1)）、CK(25℃/20℃，250μmol·m-2·s~(-1)）等4个处理，测定幼苗期形态及生理特性，不同时期、不同部位的花青素，以及果期果实的品质。【结果】低温弱光胁迫对幼苗生长存在显著影响，在幼苗期低温对幼苗生长及生理影响显著大于弱光及低温弱光，花青素含量均表现为根<叶片<叶脉<茎；在花期，花青素含量依次为花萼<花瓣；在果期，花青素含量依次为果肉<果柄<果皮。茄子不同时期受到胁迫后，不同部位的花青素含量均呈现弱光
Keyword ：
不同时期 不同时期 不同部位 不同部位 低温 低温 低温弱光 低温弱光 品质 品质 弱光 弱光 花青素 花青素
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| GB/T 7714 | 申宝营 , 吴宏琪 , 林碧英 . 低温弱光处理对茄子不同时期花青素含量及果实品质的影响 [J]. | 福建农业学报 , 2024 , 39 (03) : 310-319 . |
| MLA | 申宝营 et al. "低温弱光处理对茄子不同时期花青素含量及果实品质的影响" . | 福建农业学报 39 . 03 (2024) : 310-319 . |
| APA | 申宝营 , 吴宏琪 , 林碧英 . 低温弱光处理对茄子不同时期花青素含量及果实品质的影响 . | 福建农业学报 , 2024 , 39 (03) , 310-319 . |
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The rapid formation of the graft necrotic layer is crucial for preventing organic substance leakage and warding off external infections, significantly enhancing both the speed and quality of graft healing. This study investigates the impact of LED supplementary lighting on pumpkin-cucumber grafts, unveiling the molecular processes underlying necrotic layer formation. Specifically, three replications were conducted, where post-grafting cucumber seedlings were placed separately in healing chambers with LED light intensities of 0 mu mol/(m2 & sdot;s) and 50 +/- 1 mu mol/(m2 & sdot;s) for three days. Anatomical observations, enzyme activity assays, energy product content detection, and a more comprehensive transcriptome sequencing analysis on the graft union of the rootstock and scion were conducted. Anatomical observations revealed that LED supplementary lighting accelerates the formation of the pumpkin-cucumber graft necrotic layer, establishing a complete layer by the second day post-grafting, one day earlier than the control. Additionally, at day 3 post-grafting, the activities of POD and PPO enzymes at the rootstock-scion junction significantly surpassed the control, exhibiting a remarkable increase of 74.12 % and 48.96 %, respectively (p < 0.01). Moreover, soluble sugar and ATP levels were notably higher at day 3 postgrafting in comparison to the control, showing significant differences (p < 0.05). Transcriptomic analysis unveiled that LED supplementary lighting not only enhances scion sugar metabolism but also stimulates the upregulation of sugar synthesis genes (SPP1, RPV1) and starch synthesis genes (AGPS1, WAXY, SBEII), while downregulating the starch degradation gene LECRK71 when compared to the control. This orchestrated modulation leads to the accumulation of sugars and starch, providing substantial energy and material foundation for necrotic layer formation. Furthermore, LED supplementation also influences the hormone signaling transduction pathway in the scion, notably upregulating the gene Os01g0656200 involved in abscisic acid signaling when compared to the control, thereby furthering the formation of the necrotic layer. Overall, our research showed that LED supplementary lighting accelerates the formation of the necrotic layer in pumpkin-cucumber grafts by enhancing enzyme activities, sugar metabolism, genetic pathways related to starch accumulation, and influencing hormone signal transduction pathways, notably upregulating genes involved in abscisic acid signaling, providing a robust molecular foundation for early necrotic layer development compared to control conditions. These research findings not only provide a valuable reference for understanding graft healing mechanisms but also demonstrate the promising prospects of LED modern seedling technology. Additionally, the research, which is limited to specific pumpkin and cucumber varieties in graft experiments, necessitates further exploration to validate its broader applicability across diverse plant varieties and grafting methods.
Keyword ：
Graft healing Graft healing LED supplementation LED supplementation Molecular mechanism Molecular mechanism Necrotic layer Necrotic layer Pumpkin -cucumber Pumpkin -cucumber
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| GB/T 7714 | Zhong, Luming , Hao, Siyi , Zhai, Tingkai et al. The role of LED supplementary lighting in promoting graft necrotic layer formation in pumpkin-cucumber grafts [J]. | SCIENTIA HORTICULTURAE , 2024 , 330 . |
| MLA | Zhong, Luming et al. "The role of LED supplementary lighting in promoting graft necrotic layer formation in pumpkin-cucumber grafts" . | SCIENTIA HORTICULTURAE 330 (2024) . |
| APA | Zhong, Luming , Hao, Siyi , Zhai, Tingkai , Yang, Yongsen , Lin, Huangfang , Lin, Biying et al. The role of LED supplementary lighting in promoting graft necrotic layer formation in pumpkin-cucumber grafts . | SCIENTIA HORTICULTURAE , 2024 , 330 . |
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In plant grafting, the reconnection of vascular bundles between the rootstock and scion not only establishes functional xylem and phloem connections, but also signifies the completion of graft healing. In our previous studies focused on early-stage morphology and physiology of grafted seedlings, we have demonstrated that utilizing light intensities of 50-100-150 mu mol/(m2 center dot s) during days 1-3, 4-6, and 7-9 optimizes cucumber/pumpkin graft healing. To further explore the underlying mechanisms, we investigate light intensity regimes: 50-100-100 mu mol/(m2 center dot s) and 50-100-150 mu mol/(m2 center dot s) during the same time frames (days 1-3, 4-6, and 7-9 after grafting), denoted as CK and T treatments. Initially, we observe histological characteristics of vascular bundle formation under these conditions, followed by the analyses of superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), glutathione peroxidase (GSH-Px) enzyme activities, ascorbic acid (AsA) content in the antioxidant system, and the sequencing of transcriptome and metabolome. It is found that grafted seedlings under the T treatment achieve faster vascular bundle reconnection and shorter healing process compared to those under the CK treatment. Enzyme activities (POD, SOD, GSH-Px) increase over time under both light regimes, while CAT activity and AsA content decrease. Notably, by the 9th day, the T treatment (T9d) exhibits higher SOD, POD and CAT activities than the CK treatment (CK9d). Our findings indicate that increasing light intensity during the days 7-9 after grafting can mitigate oxidative damage at the grafting site and benefit vascular bundle reconnection. Transcriptome and metabolome analyses show the up-regulations of Cinnamaldehyde in the phenylpropanoid biosynthesis pathway, the PHGDH gene and L-Homocysteine in the cysteine and methionine metabolism pathway under T treatment in the days 7-9 after grafting. These enhance the antioxidant enzyme activities and reduce the oxidative damage to the grafting site. Additionally, GAE-related genes, and metabolites D-Xylose and Undecaprenyl phosphatealpha-L-Ara4FN in the amino sugar and nucleotide sugar metabolism pathways are also up-regulated under T treatment. The ethylene responsive factor (ERF) transcription factor CsaRAP2.3 positively regulates Undecaprenyl phosphatealpha-L-Ara4FN expression, promoting cell wall synthesis and therefore accelerating vascular bundle reconnection. In summary, during the vascular bundle formation period of cucumber graft healing, both light intensity modes coordinate regulation of phenylpropanoid biosynthesis, cysteine and methionine metabolism, amino sugar and nucleoside sugar metabolism, and ERF transcription factors, promoting graft healing from both stress resistance and cell wall synthesis. Furthermore, building upon the light intensity applied during the callus formation phase, increasing the light intensity during the vascular bundle formation period can significantly enhance cell wall synthesis, thus expediting the graft healing process. Nonetheless, the generalizability of these research findings to other grafting techniques and species requires further investigation.
Keyword ：
Cucumber Cucumber Grafting Grafting Light intensity mode Light intensity mode Vascular bundle formation stage Vascular bundle formation stage
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| GB/T 7714 | Lin, Huangfang , Zhong, Luming , Shao, Qingqing et al. Analyzing the temporal response mechanisms of the vascular bundles formation of grafted cucumber to different light intensity modes: A joint transcriptomic and metabolomic approach [J]. | SCIENTIA HORTICULTURAE , 2024 , 338 . |
| MLA | Lin, Huangfang et al. "Analyzing the temporal response mechanisms of the vascular bundles formation of grafted cucumber to different light intensity modes: A joint transcriptomic and metabolomic approach" . | SCIENTIA HORTICULTURAE 338 (2024) . |
| APA | Lin, Huangfang , Zhong, Luming , Shao, Qingqing , Cheng, Saichuan , Zhai, Tingkai , Lin, Honghui et al. Analyzing the temporal response mechanisms of the vascular bundles formation of grafted cucumber to different light intensity modes: A joint transcriptomic and metabolomic approach . | SCIENTIA HORTICULTURAE , 2024 , 338 . |
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为探究光质与钾浓度交互对紫叶生菜生长、品质的影响，进而筛选紫叶生菜最适光质与钾浓度交互模式。试验以‘紫罗马’紫叶生菜为试验材料，以白色荧光灯（L1）为对照，另设3种LED光质处理；同时基于Hoagland营养液配方，设置6个钾浓度处理，共24个处理。光质处理30 d后采收并测定紫叶生菜生物量、营养及品质相关指标。结果表明，不同光质与钾浓度交互模式对紫叶生菜生长、营养与品质存在一定影响。（1）生长方面，不同光质与60、90、120、150μg·mL
Keyword ：
交互模式 交互模式 光质 光质 品质 品质 生长 生长 紫叶生菜 紫叶生菜 钾浓度 钾浓度
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| GB/T 7714 | 林黄昉 , 庄团达 , 申宝营 et al. 光质与钾浓度交互模式对紫叶生菜生长、营养与品质的影响 [J]. | 西北农业学报 , 2024 , 33 (12) : 2295-2305 . |
| MLA | 林黄昉 et al. "光质与钾浓度交互模式对紫叶生菜生长、营养与品质的影响" . | 西北农业学报 33 . 12 (2024) : 2295-2305 . |
| APA | 林黄昉 , 庄团达 , 申宝营 , 林碧英 . 光质与钾浓度交互模式对紫叶生菜生长、营养与品质的影响 . | 西北农业学报 , 2024 , 33 (12) , 2295-2305 . |
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为探究不同波长蓝光对紫叶生菜生长品质和花青素含量的影响，以红皱品种紫叶生菜为研究对象，以白光(CK)为对照，设置蓝光峰值波长为410 nm(BO)、450 nm(BF)、480 nm(BE)的3种红蓝光组合处理，各处理光照强度均为240μmol/(m~2·s),不同波峰蓝光处理下红(660 nm)蓝光比均为1∶2,研究4种光照条件对紫叶生菜生长、花青素合成及营养品质的影响。结果表明，紫叶生菜的鲜质量随着蓝光峰值波长增加，呈现先降低后上升的趋势。在不同波长蓝光处理下，峰值为410 nm照射下的紫叶生菜生物量最大。相对于对照组的处理，在不同波长蓝光处理下叶片表面颜色表现有所不同。其中，在蓝光波长为450 nm处理下的紫叶生菜叶片颜色用色差仪测出的a值最大，相较于波长为410、480 nm蓝光处理分别提高了222.00倍和2.84倍。此外，不同波长蓝光照射可促进全生长期可溶性蛋白、花青素、类黄酮和总酚的积累。其中，450 nm蓝光处理下其含量最高，在处理16 d,相较于CK花青素含量提高了128%,可溶性蛋白含量提高了41%,类黄酮含量提高了71%,总酚含量提高了13%。不同波长蓝光也刺激了苯丙氨酸解氨酶(PAL)活性，相较于白光处理，分别提高了8%、33%、20%。综上所述，不同波长蓝光处理均促进了次生代谢物的堆集，但在波长为450 nm的蓝光处理下紫叶生菜的次生代谢产物含量最高。因此，在植物工厂中采用红光和不同波长蓝光，可以有目的地调整生菜的生长和品质。
Keyword ：
品质 品质 波长 波长 紫叶生菜 紫叶生菜 花青素 花青素 蓝光 蓝光
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| GB/T 7714 | 熊伟任 , 雷雨田 , 杨永森 et al. 不同波长蓝光对紫叶生菜品质形成的影响 [J]. | 江苏农业科学 , 2023 , 51 (01) : 143-148 . |
| MLA | 熊伟任 et al. "不同波长蓝光对紫叶生菜品质形成的影响" . | 江苏农业科学 51 . 01 (2023) : 143-148 . |
| APA | 熊伟任 , 雷雨田 , 杨永森 , 胡永波 , 林碧英 , 申宝营 . 不同波长蓝光对紫叶生菜品质形成的影响 . | 江苏农业科学 , 2023 , 51 (01) , 143-148 . |
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本文对工厂化生产的亮腹釉小蜂Tamarixiaradiata(Waterston)成虫产品进行了一系列检测，检测物种形态及分子特征、外观（体色暗淡率、残肢残翅率）、产品数量、雌蜂率、寄生率及不同温度下（15℃、25℃及30℃）亮腹釉小蜂贮存死亡率共7个质量指标，并根据检测结果提出了亮腹釉小蜂产品的质量标准。结果表明，亮腹釉小蜂规模化生产的产品应符合以下标准：形态特征吻合，分子序列（COI、ITS-1和ITS-2）相似度≥97%，体色暗淡率≤2%、残肢残翅率≤1%、实际数量占标识数量的比率≥95%、雌蜂率≥70%、不同温度下贮存死亡率均≤5%、寄生率≥90%。本标准各项指标的准确性和专属性强、灵敏度高，具有较高可行性，可用于亮腹釉小蜂质量控制和质量管理。
Keyword ：
产品 产品 亮腹釉小蜂 亮腹釉小蜂 工厂化生产 工厂化生产 质量标准 质量标准
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| GB/T 7714 | 陈玲玲 , 黄承志 , 毛润乾 et al. 亮腹釉小蜂产品的质量标准 [J]. | 中国生物防治学报 , 2022 , 38 (04) : 1030-1036 . |
| MLA | 陈玲玲 et al. "亮腹釉小蜂产品的质量标准" . | 中国生物防治学报 38 . 04 (2022) : 1030-1036 . |
| APA | 陈玲玲 , 黄承志 , 毛润乾 , 修宝林 , 高晶 , 叶凤娴 et al. 亮腹釉小蜂产品的质量标准 . | 中国生物防治学报 , 2022 , 38 (04) , 1030-1036 . |
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