灌浆期高温和水分逆境对冬小麦籽粒蛋白质和淀粉含量的影响

灌浆期高温和水分逆境是影响小麦籽粒产量和品质的关键气候因子。以扬麦9号、徐州26和豫麦34三个小麦品种为材料,利用人工气候室模拟灌浆期高温和水分胁迫环境,研究了花后高温及温度和水分互作对小麦籽粒蛋白质和淀粉形成的影响。结果表明,高温显著提高了小麦籽粒蛋白质含量及清蛋白、球蛋白和醇溶蛋白含量,但降低了谷蛋白含量,导致麦谷蛋白／醇溶蛋白比值降低。高温显著降低了籽粒总淀粉和支链淀粉含量及支／直比。籽粒蛋白质和淀粉及其组分形成所需的适宜昼夜温差随小麦品质类型而异,但温度水平对籽粒蛋白质和淀粉的影响较温差大。在高温和水分逆境下,温度对籽粒蛋白质和淀粉含量的影响较水分逆境大,且存在显著的互作效应。小麦籽粒蛋白质含量均表现为干旱〉对照〉渍水,以高温干旱最高,适温渍水最低;淀粉含量为对照〉干旱〉渍水,以适温对照最高,而高温渍水最低。高温和水分逆境显著提高了籽粒醇溶蛋白含量而降低了谷蛋白含量及支链淀粉含量,使蛋白质谷／醇比和淀粉支／直比降低,以高温渍水对籽粒蛋白质和淀粉组分的影响最为显著。不同品种之间,高蛋白小麦籽粒蛋白质和组分的形成受高温和水分逆境的影响更大,而低蛋白品种籽粒淀粉形成显著受温度和水分逆境的调节。分析表明,在高温和水分逆境下籽粒蛋白质含量与清蛋白和醇溶蛋白显著正相关,籽粒淀粉含量与谷蛋白、支链淀粉含量及支／直比显著正相关。     

花后干旱或渍水下氮素供应对小麦光合和籽粒淀粉积累的影响

防雨池栽条件下,设置渍水、干旱和对照3个土壤水分处理,每水分处理下再设置两个施氮水平,研究了花后渍水和干旱逆境下氮素水平对两个蛋白质含量不同的小麦品种光合特性和籽粒淀粉积累的影响.结果表明,与对照相比,花后渍水和干旱处理显著降低小麦旗叶净光合速率和SPAD值,干物质积累量下降.干旱处理下,增施氮肥提高旗叶光合速率和SPAD值,渍水处理下则相反.水分逆境明显降低籽粒可溶性总糖含量,且渍水处理下增施氮肥降低小麦叶片和籽粒可溶性总糖含量,干旱状态下规律相反.渍水处理下增施氮肥降低淀粉积累速率.水分逆境明显降低小麦粒重、产量和淀粉产量,且干旱处理下增施氮肥有利于籽粒重、产量和淀粉产量的提高,而渍水下增施氮肥使粒重和产量进一步降低.试验结果表明,花后渍水和干旱逆境下施用氮肥对小麦旗叶光合速率和籽粒淀粉积累有明显的调节效应.     

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。     

高温、干旱及其互作对两个筋力小麦品种淀粉糊化特性的影响

以强筋和弱筋的两个代表性小麦品种为材料,采用盆栽与人工气候箱模拟的方法,研究了花后不同时期高温、干旱及其互作对籽粒淀粉糊化特性的影响。结果表明,高温和干旱均显著影响淀粉糊化特性,但两品种表现有所不同:高温胁迫使强筋小麦品种豫麦34的峰值黏度、最终黏度(除花后5 d外)、稀懈值(除花后15 d外)和反弹值显著增大;而弱筋小麦品种豫麦50低谷黏度和最终黏度显著下降,其峰值黏度、反弹值变化不明显,从不同时期看,花后15 d影响较大。干旱胁迫使豫麦34多数黏度参数增大;而使豫麦50峰值黏度、反弹值和稀懈值下降,其低谷黏度和最终黏度在灌浆前期和中期干旱胁迫下增大,后期干旱胁迫则明显下降。研究结果还表明,花后高温与干旱胁迫对小麦黏度参数的影响存在显著的互作效应。从F值大小看,互作对弱筋小麦品种豫麦50多数黏度参数影响较大,而对强筋小麦品种豫麦34淀粉黏度参数影响较小,反映了高温、干旱及其互作对小麦淀粉特性的影响存在着显著的基因型差异。     

不同水分条件下氮素供应对小麦植株氮代谢及籽粒蛋白质积累的影响

土壤水分逆境是限制小麦籽粒品质形成的重要生态因子,明确土壤水分逆境下小麦籽粒品质形成的生理机制及调优技术途径,对于深化小麦品质生理生态研究和指导小麦调优栽培具有重要的理论意义和应用前景。在防雨池栽条件下,设置渍水、干旱和对照3个水分处理,每个水分处理下再设置120和240 kg.hm-2两个施氮水平,研究了花后渍水和干旱逆境下氮素对两个籽粒蛋白质含量不同的小麦品种植株氮代谢和籽粒蛋白质积累的影响。结果表明,与正常水分处理相比,花后干旱和渍水均降低旗叶硝酸还原酶活性、叶片总氮含量和游离氨基酸含量。干旱处理提高了茎鞘总氮与游离氨基酸含量以及籽粒蛋白质含量,而渍水处理则使其降低。水分逆境下增施氮肥提高旗叶硝酸还原酶活性、叶片与茎鞘总氮和游离氨基酸含量以及籽粒游离氨基酸和蛋白质含量。花后干旱和渍水均显著降低了小麦籽粒产量和蛋白质产量。增施氮肥提高适宜水分和水分亏缺条件下小麦籽粒产量,但不利于渍水下小麦产量的提高。这说明,花后渍水和干旱逆境下施用氮肥对小麦植株氮代谢和籽粒蛋白质积累有明显的调节效应。     

花后干旱和渍水对不同品质类型小麦籽粒品质形成的影响

 防雨池栽条件下研究了花后干旱和渍水胁迫对两个不同品质类型小麦（Triticum aestivum）品种籽粒产量和品质形成的影响。结果表明,花后渍水和干旱处理明显降低了小麦籽粒产量和蛋白质产量。在整个灌浆期内干旱处理明显提高了籽粒蛋白质和醇溶蛋白含量,而渍水处理降低了籽粒蛋白质及其组分的积累量。籽粒总淀粉和直链淀粉含量以渍水处理最高,而支链淀粉以对照最高。干旱处理提高了籽粒干、湿面筋含量、沉降值和降落值,而渍水处理降低了上述品质指标。试验表明干旱和渍水胁迫对小麦籽粒蛋白质与淀粉的含量和组分及面粉品质等均有不同程度的影响,从而改变了不同品质类型小麦的籽粒品质。     

小麦花后水分亏缺和复水对同化物转运和籽粒灌浆的影响

为了阐明水分亏缺对小麦花后同化物转运和籽粒灌浆的影响及其生理机制的相关变化,以盆栽小麦旱作品种‘长旱58’为材料,自花后9 d起,设置正常供水(WW)、中度干旱胁迫后复水(MD)和重度干旱胁迫后复水 (SD)3个水分处理,比较干旱胁迫后复水处理对小麦籽粒产量、产量构成因素及水分利用效率、强弱势粒灌浆动态、旗叶光合性能、茎鞘非结构性碳水化合物(NSC)转运、籽粒形成关键酶活性变化等的影响。结果表明：(1)与WW相比,MD处理显著增加了小麦穗粒数和千粒重,进而提高籽粒产量、水分利用效率和小麦弱势粒的最大灌浆速率和平均灌浆速率,对强势粒则无显著影响,而SD处理则显著降低了穗粒数、千粒重、强弱势粒的最大灌浆速率和平均灌浆速率,但水分利用效率显著高于WW处理。(2)MD处理植株旗叶在小麦灌浆过程中维持了与WW基本相同的净光合速率,同时在小麦花后9~20 d时MD处理下气孔导度和蒸腾速率变化不明显,而在SD处理下气孔导度和蒸腾速率则急剧下降;另外,与WW相比,在整个灌浆期MD处理下旗叶叶绿素含量变化不显著,而SD处理下叶绿素含量呈大幅下降趋势。(3)MD处理提高了小麦弱势粒蔗糖合成酶和腺苷二磷酸葡萄糖焦磷酸化酶活性;同时使灌浆中后期有较高的果聚糖水解酶(FEH)活性和较低果聚糖含量,显著增强了茎鞘同化物质转运,提高茎鞘储藏物质对粒重的贡献率。研究发现,中度水分胁迫后复水处理小麦植株具有较好的叶片性能、花后较多的茎鞘同化物向籽粒转运以及较高的弱势粒库活性,从而提高旱作小麦弱势粒灌浆速率,增加穗粒数和粒重, 进而提高籽粒产量。     

强筋与弱筋小麦籽粒蛋白质组分与加工品质对灌浆期弱光的响应

选用强筋小麦品种济麦20和弱筋小麦品种山农1391,在大田试验条件下,分别于籽粒灌浆前期(花后6—9 d)、中期(花后16—19 d)和后期(花后26—29 d)对小麦进行弱光照处理,研究了籽粒产量、蛋白质组分及加工品质的变化。灌浆期弱光显著降低小麦籽粒产量,灌浆中期对济麦20和灌浆后期对山农1391的产量降幅最大。弱光处理后,籽粒氮素积累量及氮素收获指数减少。但弱光使籽粒蛋白质含量显著升高,其中灌浆中期弱光升幅最大,原因可能是由于其粒重降低造成的。弱光对可溶性谷蛋白无显著影响,但增加不溶性谷蛋白含量,使谷蛋白聚合指数显著升高,面团形成时间和稳定时间亦升高,籽粒灌浆中、后期弱光对上述指标的影响较前期大。灌浆期短暂的弱光照对改善强筋小麦粉质仪参数有利,但使弱筋小麦变劣;并均伴随籽粒产量的显著降低这一不利影响。     

灌浆期高温对冬小麦籽粒氨基酸含量和组成的影响

以强筋小麦品种郑麦366和中筋小麦品种洛旱2号为材料,采用盆栽和人工气候室模拟的方法,研究了花后不同时段(灌浆前期即花后5 d,灌浆中期即花后15 d)和持续时间(处理2 d和4 d)的高温胁迫对籽粒氨基酸含量和积累量(以单粒中氨基酸含量表示)的影响。结果显示:(1)高温胁迫显著增加了小麦籽粒中必需氨基酸(EAA)、非必需氨基酸(NAA)和总氨基酸(TAA)含量,但降低了其积累量和EAA/TAA,2品种表现一致;(2)灌浆前期高温胁迫对2品种籽粒氨基酸含量的影响大于灌浆中期,而对氨基酸积累量的影响则相反;(3)高温持续时间对籽粒氨基酸含量的影响在2品种间存在差异,洛旱2号籽粒赖氨酸、EAA、NAA和TAA含量均随高温持续时间的延长显著增加,而郑麦366籽粒中上述指标仅在高温胁迫4 d下较对照增加显著;(4)从受高温胁迫的影响看,籽粒EAA/TAA对高温时段更敏感,而氨基酸含量表现为更易受高温持续时间的影响;(5)高温时段与持续时间的互作效应体现在:灌浆前期籽粒氨基酸积累量2品种均以高温胁迫4 d的影响最大,而灌浆中期则均以高温2 d的降幅最大。上述结果表明,小麦籽粒氨基酸及其组分对高温胁迫的响应不仅在品种间存在差异,且受高温时段和持续时间的影响。     

小麦籽粒发育及淀粉晶体特性对花后高温胁迫的响应

选用2个品质类型和成熟期不同的新疆主栽小麦品种‘新春11号’和‘新春39号’,分别进行花后灌浆早期高温(花后5~8d,32℃,T_1)和中期高温(花后15~18d,38℃,T_2)处理,分析花后高温对小麦籽粒发育及淀粉晶体的影响。结果显示:(1)T_1处理明显降低了两品种籽粒长度和粒重,而T_2处理显著影响籽粒宽度和厚度;高温处理虽然降低了籽粒灌浆速率,但两品种灌浆最大峰值出现时间均在花后18d。(2)T_1处理对小麦籽粒A型淀粉粒形态的影响较大,中熟品种‘新春11号’的A型淀粉粒表面在花后10d时可观察到微孔,在花后15~20d时其粒径明显小于同期对照,在花后20~25d时淀粉粒表面压痕增多且A、B型淀粉粒表面出现明显缢缩;而早熟品种‘新春39号’淀粉粒形态和粒径大小受花后高温的影响相对较小。(3)两品种在不同高温处理下,其淀粉粒晶体特性衍射峰出现的位置相同,但淀粉粒的尖峰强度不同,表明高温胁迫不影响淀粉粒的晶体类型,但可能改变了淀粉粒内部的层状结构。研究表明,花后早期高温不仅对小麦籽粒外部形态有较大的影响,同时也影响到籽粒内部淀粉粒的形态和晶体的特性。     

Degradation and conversion of somatostatin in normal and diabetic rats in vivo and in vitro

Plasma somatostatin-like immunoreactivity in the portal and jugular veins of streptozotocin diabetic rats was compared with that in normal control rats. In the diabetic group, somatostatin levels in the portal (p less than 0.05) and jugular (p less than 0.01) veins were both elevated compared with those in the control group. Moreover, the degree of elevation was greater in the jugular vein than in the portal vein. To further investigate the role of the liver in the clearance of somatostatin-28 in vivo, 2 micrograms of somatostatin-28 was administered as a bolus into the external jugular vein of intact and functionally hepatectomized rats. The mean half-time of somatostatin-28 was significantly longer in intact diabetic rats than in controls (p less than 0.05). The functional hepatectomy did not cause a significant difference in the half-time in diabetic rats but made it longer in control rats. These results suggest that the longer half-time of somatostatin-28 in diabetic rats in vivo is due to its slower hepatic clearance. The hepatic clearance of somatostatin-28 and somatostatin-14 was further studied in vitro using a recirculating liver perfusion method. The hepatic clearance of 1.2 nM of either somatostatin-28 or somatostatin-14 was significantly lower in diabetic rats than in controls (p less than 0.01). This indicates that elevated plasma somatostatin levels in diabetic rats are caused at least in part by decreased hepatic clearance of somatostatin.(ABSTRACT TRUNCATED AT 250 WORDS)     

Production of arsine and methylarsines in soil and in culture

Arsenate, arsenite, monomethylarsonate, and dimethylarsinate were added to different soils, and evolution of gaseous arsenical products was determined over 3 weeks. Arsine was produced in all three soils from all substrates, whereas methylarsine and dimethylarsine were produced only from methylarsonate and dimethylarsinate, respectively. At least three times more arsine than dimethylarsine was produced in soil incubated with dimethylarsinate. Resting cell suspensions of Pseudomonas and Alcaligenes produced arsine as the sole product when incubated anaerobically in the presence of arsenate or arsenite. In all instances, no trimethylarsine was observed, nor could any evidence be shown for the methylation of any arsenical substrate in soil or in culture. It was concluded that reduction to arsine, not methylation to trimethylarsine, was the primary mechanism for gaseous loss of arsenicals from soil.     

Growth and mitogenic effects of arylphorin in vivo and in vitro

In insects, developmental responses are organ- and tissue-specific. In previous studies of insect midgut cells in primary tissue cultures, growth-promoting and differentiation factors were identified from the growth media, hemolymph, and fat body. Recently, it was determined that the mitogenic effect of a Manduca sexta fat body extract on midgut stem cells of Heliothis virescens was due to the presence of monomeric alpha-arylphorin. Here we report that in primary midgut cell cultures, this same arylphorin stimulates stem cell proliferation in the lepidopterans M. sexta and Spodoptera littoralis, and in the beetle Leptinotarsa decemlineata. Studies using S. littoralis cells confirm that the mitogenic effect is due to free alpha-arylphorin subunits. In addition, feeding artificial diets containing arylphorin increased the growth rates of several insect species. When tested against continuous cell lines, including some with midgut and fat body origins, arylphorin had no effect; however, a cell line derived from Lymantria dispar fat body grew more rapidly in medium containing a chymotryptic digest of arylphorin.     

Antiplatelet and antithrombotic activities of purpurogallin in vitro and in vivo

Enzymatic oxidation of pyrogallol was efficiently transformed to an oxidative product, purpurogallin (PPG). Here, the anticoagulant activities of PPG were examined by monitoring activated partial thromboplastin time (aPTT), prothrombin time (PT), and the activities of thrombin and activated factor X (FXa). And, the effects of PPG on expression of plasminogen activator inhibitor type 1 (PAI-1) and tissue-type plasminogen activator (t-PA) were evaluated in tumor necrosis factor (TNF)-α activated human umbilical vein endothelial cells (HUVECs). Treatment with PPG resulted in prolonged aPTT and PT and inhibition of the activities of thrombin and FXa, as well as inhibited production of thrombin and FXa in HUVECs. In addition, PPG inhibited thrombin-catalyzed fibrin polymerization and platelet aggregation. PPG also elicited anticoagulant effects in mice. In addition, treatment with PPG resulted in significant reduction of the PAI-1 to t-PA ratio. Collectively, PPG possesses antithrombotic activities and offers a basis for development of a novel anticoagulant. [BMB Reports 2014; 47(7): 376-381]     

Growth and reproduction of Arabidopsis thaliana in relation to storage of starch and nitrate in the wild-type and in starch-deficient and nitrate-uptake-deficient mutants

We have investigated the interactions between resource assimilation and storage in rosette leaves, and their impact on the growth and reproduction of the annual species Arabidopsis thaliana. The resource balance was experimentally perturbed by changing (i) the external nutrition, by varying the nitrogen supply; (ii) the assimilation and reallocation of resources from rosette leaves to reproductive organs, by cutting or covering rosette leaves at the time of early flower bud formation, and (iii) the internal carbon and nitrogen balance of the plants, by using isogenic mutants either lacking starch formation (PGM mutant) or with reduced nitrate uptake (NU mutant). When plants were grown on high nitrogen, they had higher concentrations of carbohydrates and nitrate in their leaves during the rosette phase than during flowering. However, these storage pools did not significantly contribute to the bulk flow of resources to seeds. The pool size of stored resources in rosette leaves at the onset of seed filling was very low compared to the total amount of carbon and nitrogen needed for seed formation. Instead, the rosette leaves had an important function in the continued assimilation of resources during seed ripening, as shown by the low seed yield of plants whose leaves were covered or cut off. When a key resource became limiting, such as nitrogen in the NU mutants and in plants grown on a low nitrogen supply, stored resources in the rosette leaves (e.g. nitrogen) were remobilized, and made a larger contribution to seed biomass. A change in nutrition resulted in a complete reversal of the plant response: plants shifted from high to low nutrition exhibited a seed yield similar to that of plants grown continuously on a low nitrogen supply, and vice versa. This demonstrates that resource assimilation during the reproductive phase determines seed production. The PGM mutant had a reduced growth rate and a smaller biomass during the rosette phase as a result of changes in respiration caused by a high turnover of soluble sugars ( Caspar et al. 1986 ; W. Schulze et al. 1991 ). During flowering, however, the vegetative growth rate in the PGM mutant increased, and exceeded that of the wild-type. By the end of the flowering stage, the biomass of the PGM mutant did not differ from that of the wild-type. However, in contrast to the wild-type, the PGM mutant maintained a high vegetative growth rate during seed formation, but had a low rate of seed production. These differences in allocation in the PGM mutant result in a significantly lower seed yield in the starchless mutants. This indicates that starch formation is not only an important factor during growth in the rosette phase, but is also important for whole plant allocation during seed formation. The NU mutant resembled the wild-type grown on a low nitrogen supply, except that it unexpectedly showed symptoms of carbohydrate shortage as well as nitrogen deficiency. In all genotypes and treatments, there was a striking correlation between the concentrations of nitrate and organic nitrogen and shoot growth on the one hand, and sucrose concentration and root growth on the other. In addition, nitrate reductase activity (NRA) was correlated with the total carbohydrate concentration: low carbohydrate levels in starchless mutants led to low NRA even at high nitrate supply. Thus the concentrations of stored carbohydrates and nitrate are directly or indirectly involved in regulating allocation.     

Importance of guanine nitration and hydroxylation in DNA in vitro and in vivo

Guanine (Gua) modification by nitrating and hydroxylating systems was investigated in DNA. In isolated calf thymus DNA, 8-NO(2)-Gua and 8-oxo-Gua were dose-dependently formed with peroxynitrite, and 8-NO(2)-Gua was released in substantial amounts. Myeloperoxidase (MPO) with H(2)O(2) and NO(2)(-) reacted with calf thymus DNA to form 8-NO(2)-Gua dose dependently without release of 8-NO(2)-Gua. The frequency of strand breaks was higher than the sum of 8-NO(2)-Gua and 8-oxo-Gua, particularly in the MPO-treated DNA, indicating the importance of other types of damage. The activation of human neutrophils and lymphocytes with phorbol ester did not induce 8-NO(2)-Gua and 8-oxo-Gua in their nuclear DNA. However, 8-NO(2)-Gua was found in calf thymus DNA co-incubated with activated neutrophils in the presence of NO(2)(-). No significant formation of 8-NO(2)-Gua was found in liver DNA from mice treated with Escherichia coli lipopolysaccharide. The incubation of peroxynitrite or MPO-H(2)O(2)-NO(2)(-)-treated DNA with formamidopyrimidine glycosylase (Fpg) released 8-oxo-Gua, but not 8-NO(2)-Gua, indicating that 8-NO(2)-Gua is not a substrate for Fpg. Although 8-NO(2)-Gua was generated in isolated DNA by different nitrating systems, other types of damage were formed in abundance, and the lesion could not be found reliably in nuclear DNA, suggesting that the biological importance is limited.