玉米灌浆期水分差异供应对籽粒淀粉积累及其酶活性的影响

利用普通玉米(Zay mays)‘掖单22’和高油玉米‘高油115’,研究了灌浆期水分差异供应对籽粒淀粉及其组分积累、相关酶活性动态变化的影响。结果表明,两种类型玉米淀粉积累和酶活性动态变化趋势基本一致,但对水分的反应有差异。缺水提高了‘掖单22’籽粒中淀粉、支链淀粉含量,而直链淀粉含量下降,‘高油115’则是籽粒中的淀粉含量、支链淀粉和直链淀粉含量提高;充分供水使淀粉及其组分产量提高;叶片中蔗糖合成酶(SS)、磷酸蔗糖合成酶(SPS)活性随水分供应水平而提高,尤其在授粉后10~30 d增幅更加明显。充分供水明显提高籽粒中腺苷二磷酸葡萄糖焦磷酸化酶(ADPG-PPase)、尿苷二磷酸葡萄糖焦磷酸化酶(UDPG-PPase)、可溶性淀粉合成酶(SSS)和淀粉粒结合淀粉合成酶(GBSS)活性,缺水使籽粒中酶活性下降较早且迅速;SPS、ADPG-PPase、SSS酶活性对缺水反应比较敏感。     

氮素对不同类型玉米籽粒氨基酸、蛋白质含量及其组分变化的影响

以普通玉米掖单22和高油玉米高油115为材料,研究了不同供氮条件下玉米籽粒中蛋白质及其组分的含量、清蛋白和球蛋白含量、醇溶蛋白和谷蛋白含量、籽粒氨基酸总鼍以及氨基酸组分含量的品种差异。结果表明。氮素供应水平对两种类型玉米灌浆期间籽粒蛋白质含量变化作用相同,前期逐渐下降,至成熟期略有升高;籽粒清蛋白和球蛋白、醇溶蛋白和符蛋白含量变化动态各处理基本一致,两种类型玉米籽粒清蛋白含量随时间的推移逐渐降低。球蛋门含量的变化动态旱单峰曲线,峰值出现在授粉后30d。醇溶蛋白含量均呈“V”型变化,以授粉30d后最低。谷蛋白的含量则均呈上升趋势。氮素供应水平对两种类型玉米籽粒中各蛋白质组分禽量的变化的影响作用有所不同。对高油115籽粒中球蛋白含量的影响较小;施氮水平并不改变两种类型玉米籽粒氨基酸总量的变化趋势。但两种类型玉米籽粒中氨基酸组分的含量变化较大。     

开花后小黑麦旗叶氮代谢与籽粒蛋白质形成的品种间差异

为了解不同类型小黑麦(×Triticosecale)氮代谢及籽粒蛋白质形成的差异,本文以加工型品种‘东农8809’、饲用型品种‘东农5305’和粮饲兼用型品种‘东农96026’为材料,采用随机区组设计,探究3个类型小黑麦品种氮同化、氮素积累及转运、蛋白质积累特性的变化。结果表明,加工型品种‘东农8809’花后氮素同化量高而氮素转运量低,籽粒蛋白质主要来源于花后植株的同化吸收;饲用型品种‘东农5305’硝酸还原酶(NR)和谷氨酰胺合成酶(GS)活性高,旗叶可溶性蛋白含量和游离氨基酸含量较高,对氮的贮存能力高,利于生育后期向籽粒转运;粮饲兼用型品种‘东农96026’的NR和GS活性较低,且生育后期GS降幅大,氮同化能力较低,氮素转运量和氮转运效率小,氮素转运能力弱。     

土壤水分对强筋小麦‘豫麦34’氮素同化酶活性和籽粒品质的影响

 以强筋型小麦(Triticum aestivum)品种‘豫麦34号’为材料,采用盆栽方法研究了土壤水分对氮素同化酶活性及籽粒品质的影响。结果表明：旗叶硝酸还原酶（NR）活性于花后呈下降趋势,且土壤含水量为田间持水量（FC）60%的处理活性最强,其次为40%FC,活性最低的是80%FC。旗叶和籽粒中谷氨酰胺合成酶（GS）活性于开花15 d前均呈下降趋势,15 d后均为上升趋势,各水分处理间酶活性大小关系是：80%FC＞60%FC＞40%FC。各水分处理间旗叶和籽粒谷氨酸合成酶（GOGAT）活性的大小关系同GS。60%FC籽粒产量及品质最优,80%FC产量次之,40%FC产量最低;40%FC品质次之,80%FC品质最低。不同水分处理下籽粒蛋白质含量与叶片NR、GS 和籽粒GOGAT活性均呈正相关,与旗叶GOGAT活性呈负相关。且40%FC和80%FC下籽粒蛋白质含量只与旗叶GS活性相关性达显著水平, 60%FC下蛋白质含量则与旗叶NR和籽粒GS活性均达显著相关,与旗叶GS活性达极显著相关。     

水分胁迫对水稻籽粒蛋白质积累及营养品质的影响

以生产上广泛使用的水稻(Oryza sativa)品种‘汕优63’、‘扬稻6号’和‘武育粳3号’为材料,研究了水分胁迫对结实期水稻籽粒蛋白质积累及营养品质的影响。结果表明:正常施氮水平下,花后10~20 d的水分胁迫提高了谷氨酰胺合成酶(Glutamine synthetase,GS)和谷氨酸合酶(Glutamate synthase,GOGAT)活性,提高了籽粒自身利用无机氮合成氨基酸的能力,从而利于籽粒内蛋白质的积累,而高氮水平下,水分胁迫降低了籽粒自身合成氨基酸的能力。以重量为基数的蛋白质含有率在整个灌浆过程中呈“V”型消长,正常施氮水平下,水分胁迫明显提高了花后15 d至成熟期蛋白质含有率,而高氮水平下,水分胁迫处理的蛋白质含有率明显低于水层灌溉。与水层灌溉相比,水分胁迫提高了正常施氮水平下精米中醇溶蛋白和谷蛋白含量,但却明显降低了高氮水平下精米中醇溶蛋白和谷蛋白含量。水分胁迫对稻米中赖氨酸含量的影响因品种、植株的氮营养水平的不同而不同,水分胁迫显著降低了两种氮肥水平下‘汕优63’中赖氨酸含量,但却明显提高‘扬稻6号’中赖氨酸含量;而‘武育粳3号’于两种氮肥水平下表现恰好相反,正常施氮水平下赖氨酸含量略有升高;而高氮水平下赖氨酸含量明显降低。     

结实期土壤水分亏缺影响水稻籽粒灌浆的生理原因

通过分析结实期土壤水分亏缺对水稻(Oryza sativa)籽粒中蔗糖向淀粉合成的生理代谢中关键酶活性及籽粒灌浆的调节作用, 探讨土壤水分亏缺影响水稻籽粒灌浆的生理机制。结果表明, 适度土壤水分亏缺诱导了灌浆高峰期(花后15-20天)水稻籽粒中蔗糖合成酶、腺苷二磷酶葡萄糖焦磷酸化酶、可溶性淀粉合成酶及淀粉分支酶活性的增加, 提高了籽粒灌浆中前期(花后10-20天)籽粒中淀粉积累速率和籽粒灌浆速率。但在灌浆后期(花后20-30天)籽粒中, 上述关键酶活性下降较快, 籽粒活跃灌浆期明显缩短, 灌浆前中期灌浆速率的增加不能完全补偿灌浆期缩短带来的同化物积累损失, 导致水分亏缺处理水稻籽粒充实不良, 结实率、籽粒重和产量显著降低。研究认为, 灌浆期土壤水分亏缺引起的灌浆后期籽粒中蔗糖向淀粉合成代谢中一些关键酶活性快速下降和籽粒内容物的供应不足是籽粒淀粉积累总量减少、粒重降低的主要生理原因。     

不同生育期花生叶片蛋白质含量及氮代谢相关酶活性分析

以5个珍珠豆型花生(Arachis hypogaea Linn.)品种(系)‘汕E’(‘Shan E’)、‘汕G’(‘Shan G’)、‘TH’、‘TJ’和‘泉花7号’(‘Quanhua No.7’)为研究对象,分析了花针期、结荚期和饱果期花生叶片中可溶性蛋白质含量及硝酸还原酶(NR)、谷氨酰胺合成酶(GS)和谷氨酸脱氢酶(GDH)活性的变化趋势,并比较了5个品种(系)荚果和秆产量的差异。结果表明:在3个生育期内,5个花生品种(系)叶片可溶性蛋白质含量和GDH活性的变化趋势基本一致,而NR和GS活性的变化趋势则有差异。其中,可溶性蛋白质含量均呈"低—高—低"的变化趋势,在结荚期最高;GDH活性均逐渐升高,至饱果期达最高;‘泉花7号’叶片NR活性呈"高—低—高"的变化趋势,而其他4个品种(系)叶片NR活性均逐渐降低;‘汕E’、‘TJ’和‘泉花7号’叶片GS活性呈逐渐降低趋势,而‘汕G’和‘TH’叶片GS活性呈"低—高—低"的变化趋势。总体上看,5个品种(系)中,‘汕G’和‘泉花7号’叶片的可溶性蛋白质含量及NR和GDH活性、‘汕E’叶片的NR和GS活性以及‘TH’叶片的GDH活性均较高。5个品种(系)的2个产量指标(单株荚果鲜质量和单株秆鲜质量)均有明显差异,总体上看,‘汕G’、‘泉花7号’和‘TH’的2个产量指标均较高,而‘汕E’和‘TJ’的2个产量指标均较低。综合分析结果显示:‘汕G’和‘泉花7号’叶片可溶性蛋白质含量及NR和GDH活性均相对较高,其荚果和秆产量也均较高,表明花生荚果和秆产量与不同生育期叶片氮代谢水平有一定关系。     

灌浆前期高温和干旱胁迫对小麦籽粒蛋白质含量和氮代谢关键酶活性的影响

为探讨花后逆境胁迫影响小麦籽粒氮代谢及蛋白质合成的生理机制,采用盆栽和人工气候室模拟花后高温的方式,研究了灌浆前期短暂高温和干旱胁迫对两个不同品质类型小麦品种籽粒蛋白质含量、组分及谷氨酰胺合成酶(GS)、谷丙转氨酶(GPT)活性的影响。结果表明,灌浆前期高温、干旱及其复合胁迫均显著提高两品种籽粒蛋白质及组分含量,但降低谷/醇比。逆境胁迫使蛋白质积累量和粒重显著下降,其中高温处理使两品种蛋白质产量分别下降20.7%和12.4%,粒重下降23.2%和24.0%;干旱胁迫使两品种蛋白质产量分别下降16.2%和11.9%,粒重下降18.0%和16.0%;复合胁迫使两品种蛋白质产量分别下降26.1%和15.8%,粒重下降29.9%和28.9%。高温、干旱及其复合胁迫下两品种籽粒氮代谢关键酶活性升高。花后8,17,23,29 d的GS活性和花后11,17 d的GPT活性与蛋白质含量呈显著或极显著正相关,花后23,35 d的GS和花后8,17,23 d的GPT活性与蛋白质产量呈显著或极显著负相关,花后8,17,23,29,35 d的GS和花后8,11,17,23 d的GPT活性与籽粒产量呈显著或极显著负相关。试验条件下,高温处理对籽粒蛋白质合成的影响大于干旱胁迫,二者具有叠加效应,强筋小麦品种郑麦366受逆境胁迫的影响较大。     

不同类型春玉米灌浆期间籽粒中内源激素IAA、GA、ZR、ABA含量的变化

田间种植的高淀粉（‘郑单19’）、高油（‘通油1号’）和普通型（‘吉单209’）春玉米在籽粒灌浆过程中,‘郑单19’的IAA在授粉后28d达到峰值,‘吉单209’和‘通油1号’的峰值出现在35d;在3个杂交种中,‘郑单19’的IAA峰值最大,‘吉单209’次之,‘通油1号’最低;整个籽粒灌浆期间,‘通油1号’和‘吉单209’的GA含量高于‘郑单19’,在灌浆后期,‘通油1号’仍保持较高的GA含量;‘通油1号’ZR含量的峰值最高,直到后期仍保持较高的水平;‘郑单19’在籽粒灌浆前期的ABA含量较低,但在后期的含量较高。     

花后土壤水分状况对小麦籽粒淀粉和蛋白质积累关键调控酶活性的影响

在温室盆栽条件下,以2个不同蛋白质含量的冬小麦(Triticum aestivum L．)品种皖麦38和扬麦9为材料,研究了花后第4天开始的土壤干旱(SRWC=45％～50％)和渍水对籽粒蛋白质和淀粉积累关键调控酶活性的影响。小麦叶片和籽粒的测定结果均表明,小麦源库器官中籽粒蛋白质和淀粉积累的关键调控酶活性变化趋势在2个品种间基本一致。与对照(SRWC=75％～80％)相比,干旱和渍水均明显降低了花后旗叶中蔗糖含量和磷酸蔗糖合成酶(SPS)活性,而氨基酸含量和谷氨酰胺合成酶(GS)活性略有下降。干旱和渍水均降低了籽粒库蔗糖合成酶(SS)和结合态淀粉合成酶(GBSS)活性,可溶性淀粉合成酶(SSS)活性降低尤甚。其中干旱处理下SS的下降比渍水更为明显。与对照相比,渍水明显降低了籽粒谷丙转氨酶(GPT)和GS活性,而干旱的影响较小。相关性分析结果表明籽粒淀粉产量和含量与SPS,SSS和GBSS活性的关系比与SS活性的关系更为密切,籽粒蛋白质产量和含量与叶中GS和籽粒中GPT活性的关系比与籽粒中GS关系活性更为密切。这些结果表明小麦源库器官中调控籽粒蛋白质和淀粉积累的关键酶活性变化是花后不同水分状况影响籽粒淀粉和蛋白质特性的重要因素。     

Effect of Subsoiling in Fallow Period on Soil Water Storage and Grain Protein Accumulation of Dryland Wheat and Its Regulatory Effect by Nitrogen Application

To provide a new way to increase water storage and retention of dryland wheat, a field study was conducted at Wenxi experimental site of Shanxi Agricultural University. The effect of subsoiling in fallow period on soil water storage, accumulation of proline, and formation of grain protein after anthesis were determined. Our results showed that subsoiling in fallow period could increase water storage in the 0–300 cm soil at pre-sowing stage and at anthesis stage with low or medium N application, especially for the 60–160 cm soil. However, the proline content, glutamine synthetase (GS) activity, glutamate dehydrogenase (GDH) activity in flag leaves and grains were all decreased by subsoiling in fallow period. In addition, the content of albumin, gliadin, and total protein in grains were also decreased while globulin content, Glu/Gli, protein yield, and glutelin content were increased. With N application increasing, water storage of soil layers from 20 to 200 cm was decreased at anthesis stage. High N application resulted in the increment of proline content and GS activity in grains. Besides, correlation analysis showed that soil storage in 40–160 cm soil was negatively correlated with proline content in grains; proline content in grains was positively correlated with GS and GDH activity in flag leaves. Contents of albumin, globulin and total protein in grains were positively correlated with proline content in grains and GDH activity in flag leaves. In conclusion, subsoiling in fallow period, together with N application at 150 kg·hm⁻², was beneficial to increase the protein yield and Glu/Gli in grains which improve the quality of wheat.     

羧甲基壳聚糖对玉米籽粒氮代谢关键酶和种子贮藏蛋白含量的影响

以羧甲基壳聚糖（ＮＣＭＣ） 处理玉米开花期果穗,发育中籽粒的谷氨酰胺合成酶（ＧＳ） 、谷氨酸脱氢酶（ＧＤＨ） 及谷丙转氨酶（ＧＰＴ） 活性均明显增强,而蛋白水解酶活性下降。羧甲基壳聚糖处理离体玉米籽粒酶提取液,酶液中ＧＤＨ 活性明显提高。羧甲基壳聚糖处理玉米果穗,其发育籽粒中可溶性蛋白和成熟种子中贮藏蛋白含量明显提高。这都表明,羧甲基壳聚糖对玉米氮代谢、蛋白质合成与积累具有明显的生理调节作用。     

有机物沟埋还田模式与花后灌水量对玉米光合特性和产量的影响

有机物沟埋还田与花后灌水配合对增加玉米田保水供水能力,提高玉米花后光合性能、实现节水增产有重要意义.本试验以郑单958为供试材料,设置有机物沟埋还田和花后灌水量两个因素,有机物沟埋还田包括不还田(M₀)、秸秆单还田(M₁)和牛粪秸秆混合还田(M₂)3个还田类型,花后灌水量包括450 mm(W₁)和325 mm(W₂)2个水平,研究了其对玉米穗位叶光合性能、光系统Ⅱ(PSⅡ)效率和产量等的影响.结果表明:与秸秆单还田比较,牛粪秸秆混合还田有效提高了玉米花后光合能力和各器官的干物质积累量;与节水灌溉相比,正常灌溉加强了有机物还田对玉米光合能力的促进作用.牛粪秸秆混合还田与正常灌溉结合可显著提高玉米花后叶片的光合速率(P_n)、气孔导度(g_s)和蒸腾速率(T_r),降低胞间CO₂浓度(C_i);提高玉米花后叶片PSⅡ的最大光化学效率(φ_po)和捕获的激子将电子传递到电子传递链中Q_A下游的电子受体的概率(Ψ_o);改善花后叶片光能利用率,维持花后叶片较高的光合性能;同时增加花后玉米各器官干物质的量,提高干物质总积累量和转运能力,有利于花后同化物对籽粒的分配,最终获得高产.节水灌溉降低了叶片的光合性能,造成产量的下降;但配合牛粪秸秆混合还田与不还田处理相比,水分利用效率、籽粒增长速率和增产效果均优于正常灌水.这表明牛粪秸秆混合还田与正常灌溉结合可有效提高玉米花后光合性能,增加干物质积累量,促进玉米增产;牛粪秸秆混合还田与节水灌溉结合一定程度上降低了因减少灌溉量造成的减产.     

Glutamate dehydrogenase and glutamine synthetase activities during the development of triticale grains

Glutamate dehydrogenase (GDH, EC 1.4.1.2–4) and glutamine synthetase (GS, EC 6.3.1.2) activities as well as protein content and dry matter in developing kernels of winter Triticale were determined. The relatively low level of GS activity compared to high level of NAD(P)H-dependent GDH activity during intensive filling of grains with storage compounds may indicate the participation of GDH in reductive amination of 2-oxoglutarate. The amination activity of this enzyme in all grain development phases exceeded the deaminating activity several fold. Moreover, the dynamics in the change of NAD(P)H-GDH and NAD(P)⁺-GDH activities were analysed in various tissues of the developing grains. The high amination activity of the enzyme in the seed coat, where the intensive protein synthesis occurs would also be an indication of the anabolic function of this enzyme.     

A study of the role of glutamate dehydrogenase in the nitrogen metabolism of Arabidopsis thaliana

Glutamate-dehydrogenase (GDH, EC 1.4.1.2) activity and isoenzyme patterns were investigated in Arabidopsis thaliana plantlets, and parallel studies were carried out on glutamine synthetase (GS, EC 6.3.1.2). Both NADH-GDH and NAD-GDH activities increased during plant development whereas GS activity declined. Leaves deprived of light showed a considerable enhancement of NADH-GDH activity. In roots, both GDH activities were induced by ammonia whereas in leaves nitrogen assimilation was less important. It was demonstrated that the increase in GDH activity was the result of de-novo protein synthesis. High nitrogen levels were first assimilated by NADH-GDH, while GS was actively involved in nitrogen metabolism only when the enzyme was stimulated by a supply of energy, generated by NAD-GDH or by feeding sucrose. When methionine sulfoximine, an inhibitor of GS, was added to the feeding solution, NADH-GDH activity remained unaffected in leaves whereas NAD-GDH was induced. In roots, however, there was a marked activation of GDH and no inactivation of GS. It was concluded that NADH-GDH was involved in the detoxification of high nitrogen levels while NAD-GDH was mainly responsible for the supply of energy to the cell during active assimilation. Glutamine synthetase, on the other hand was involved in the assimilation of physiological amounts of nitrogen. A study of the isoenzyme pattern of GDH indicated that a good correlation existed between the relative activity of the isoenzymes and the ratio of aminating to deaminating enzyme activities. The NADH-GDH activity corresponded to the more anodal isoenzymes while the NAD-GDH activity corresponded to the cathodal ones. The results indicate that the two genes involved in the formation of GDH control the expression of enzymes with different metabolic functions.Abbreviations GDH glutamate dehydrogenase - GS glutamine synthetase - MSO methionine sulfoximine