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硝普钠添加对碱胁迫下萌发期水稻碳氮代谢的影响OA北大核心CSTPCD

Effect of sodium nitroprusside addition on carbon and nitrogen metabolism of rice during germination under alkali stress

中文摘要英文摘要

[目的]施加外源硝普纳(sodium nitroprusside,SNP)可有效缓解水稻碱胁迫伤害.本研究通过比较不同碱敏感性水稻品种萌发及碳氮代谢相关指标的差异,探讨碱胁迫下外源SNP添加对萌发期水稻碳氮代谢的影响,为盐碱地水稻种植提供参考.[方法]以碱敏感品种中花 11(ZH11)和耐碱品种宁粳 52(NG52)为试验材料,在混合碱胁迫[alkali stress(AS),即 20 mmol/L CO32-和HCO3-等比例混合液,pH 10.50]下,设置不同SNP浓度(0、10、30、50、70、100 μmol/L)浸种处理,通过测定萌发期关键生长指标,以筛选SNP最适浓度.结果显示碱胁迫下不同浓度外源SNP影响了水稻萌发,其中,30 μmol/L SNP处理显著增加了水稻的发芽指数,促进了水稻萌发.进一步设置CK(control)、SNP(30 μmol/L)、AS(20 mmol/L)、AS+SNP(20 mmol/L AS+30 μmol/L SNP)4 个处理,分析它们对萌发期碱敏感差异水稻碳氮代谢的影响.[结果]1)在碳代谢方面,与AS处理相比,AS+SNP处理下ZH11 和NG52 中蔗糖含量显著降低.其中,NG52 中蔗糖含量显著低于ZH11,而其蔗糖合成基因(OsNIN1)和葡萄糖合成基因(OsSPS1、OsSPS11)的表达量显著高于ZH11.2)在氮代谢方面,与AS处理相比,AS+SNP处理显著增加了 2 个品种中苹果酸、柠檬酸、一氧化氮含量,硝酸还原酶、S-亚硝基谷胱甘肽还原酶活性以及OsNR2、OsGSNOR1 基因表达,降低了NO3-和氧化型谷胱甘肽含量,提高了脯氨酸水平.其中,NG52 中苹果酸、柠檬酸、一氧化氮、脯氨酸、氧化型谷胱甘肽含量,S-亚硝基谷胱甘肽还原酶活性以及OsNR1.2、OsGSNOR1 的表达量均显著高于ZH11.3)相关分析和主成分分析结果显示,葡萄糖和蔗糖合成酶基因(OsNIN1)分别与苹果酸、柠檬酸、脯氨酸和一氧化氮呈显著正相关,葡萄糖、果糖、一氧化氮、亚硝基谷胱甘肽和氧化型谷胱甘肽可能是影响碳氮代谢相互协调的关键指标.[结论]施加 30 μmol/L SNP可促进碱胁迫下水稻体内蔗糖分解和有机酸的积累,增强硝酸还原酶和S-亚硝基谷胱甘肽还原酶活性,提高有机氮含量,促进碳代谢向氮代谢转化,维持碱胁迫下萌发期水稻碳氮代谢的正常进行.

[Objectives]The application of exogenous sodium nitroprusside(SNP)can effectively alleviate alkali stress-induced damage in rice.We observed the effect differences of exogenous SNP on the carbon and nitrogen metabolism of rice cultivars when subjecting to alkali stress at germination satge.[Methods]Alkali sensitive rice cultivar Zhonghua 11(ZH11)and alkali resistant cultivar Ninggeng 52(NG52)was chosed as test materials in a pot experiment.Firstly,rice seeds were soaked into alkali stress solutions(containing 20 mmol/L CO32-and HCO3-,pH 10.50)containing SNP 10,30,50,70,100 μmol/L,respectively.SNP 30 μmol/L treatment was recorded the highest germination index,so was used as the SNP concentrations for the following experiment.In the following experiment,normal nutrient solution control(CK),normal solution containing SNP 30 μmol/L(SNP),alkali stress solution(AS),and alkali stress solution containing NSP 30 μmol/L(AS+SNP).The rice seeds were watered with the treatment solution,and the carbon and nitrogen metabolism of rice seedlings were measured.[Results]AS+SNP treatment were recorded significantly lower sucrose content than AS treatment in both cultivar ZH11 and NG52.The sucrose contents of NG52 were significantly lower than that of ZH11,however,the expression of genes involved in sucrose synthesis(OsNIN1)and glucose synthesis(OsSPS1 and OsSPS11)in NG52 were significantly higher than that in ZH11.Compared with AS,the AS+SNP treatment markedly increased the levels of malic acid,citric acid,nitric oxide(NO),and proline content,as well as the activities of nitrate reductase(NR)and S-nitroso glutathione reductase(GSNOR)and expression of OsNR2 and OsGSNOR1,decreased the levels of NO3-and glutathione(oxidized glutathione,GSSG)in both cultivars.Furthermore,the contents of malic acid,citric acid,NO,proline,GSSG,together with GSNOR activity and the expression levels of OsNR1.2 and OsGSNOR1 were significantly higher in NG52 compared with ZH11.Positive correlations(P<0.05)were existed between genes involved in glucose and sucrose synthesis(OsNIN1)with malic acid,citric acid,proline,and NO.The principal component analysis indicated that glucose,fructose,NO,GSNO,and GSSG were key factors affecting the coordination of carbon and nitrogen metabolism.[Conclusions]Treating rice seeds with 30 μmol/L SNP solution is effective in increasing sucrose breakdown,organic acid accumulations,NR and GSNOR activities,organic nitrogen levels,and stimulating the transformation of carbon metabolism to nitrogen metabolism,thereby maintaining the normal carbon and nitrogen metabolism of rice under alkali stress during germination.

闵炜芳;方晶莹;石亚飞;摆小蓉;舍杨梦斐;田浩天;罗成科

宁夏大学农学院/宁夏优势特色作物现代分子育种重点实验室,宁夏银川 750021

水稻萌发期碱胁迫硝普纳碳氮代谢

ricegerminationalkali stresssodium nitroprussidecarbon and nitrogen metabolism

《植物营养与肥料学报》 2024 (005)

934-947 / 14

宁夏自然科学基金项目(2023AAC03144);宁夏科技创新团队项目(2022BSB03109);宁夏大学大学生创新创业训练计划项目(S202310749101).

10.11674/zwyf.2023555

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