新型生物——人工复合血管研制的初步报告

本文设计一种由胶原和高分子聚合物组成的新型生物一人工复合血管。其研制过程是将包绕有聚酯网的硅胶棒埋入羊的皮下组织,再将形成的经聚酯网为支架的胶原管经醛化处理。作者通过肉眼和SEM观察提出了研制生物——人工复合血管的要点:聚酯网网孔要合适,其与硅胶棒的间隙要恰当,理化处理方法更要选择好。     

质体醌重组的D1／D2／Cytb559复合物的荧光衰减动力学和光破坏作用

光系统Ⅱ反应中心Ｄ１／Ｄ２／Ｃｙｔｂ５５９ 在分离纯化过程中失去了电子受体ＱＡ 和ＱＢ,人工合成的质体醌可以与Ｄ１／Ｄ２／Ｃｙｔｂ５５９ 复合物发生重组。癸基质体醌（ＤＰＱ）与Ｄ１／Ｄ２／Ｃｙｔｂ５９９ 复合物的重组导致该复合物的荧光强度下降及发射光谱蓝移,同时两个与光化学活性相关的长寿命（２４ ｎｓ和７３ ｎｓ）荧光衰减组分占整个荧光的百分数下降,这些结果表明ＤＰＱ作为Ｐｈｅｏ－ 的电子受体,限制了Ｐ６８０＋ ·Ｐｈｅｏ－ 的电荷重组。ＤＰＱ 的加入对Ｄ１／Ｄ２／Ｃｙｔｂ５５９复合物中Ｃｈｌａ 分子的光破坏敏感性影响不大,但β－胡萝卜素在加入ＤＰＱ 之后可以被光照破坏,这个过程可能与β－胡萝卜素的生理功能相关。     

高温胁迫对光系统Ⅱ异质性的影响

高温胁迫可诱导光系统Ⅱ（ＰＳⅡ）活性中心转化为无活性中心。本文讨论了在高温胁迫导致荧光猝灭的情况下如何用叶绿素荧光动力学计算ＰＳⅡ无活性中心相对含量的问题。正常的小麦叶片其ＰＳⅡ无活性中心相对含量（Ｆｖｉ／ＦＶ）约为０．１５５±０．０１１。小麦叶片经５０℃１分钟高温胁迫后,其Ｆｖｉ（相对于正常Ｆｖ）降至对照的７０％,在随后室温下６０分钟内又降至５０％。而５５℃５分钟和５５℃１０分钟高温胁迫后,在恢复期内其ＰＳⅡ无活性中心的含量从常温的１．４倍左右的基础上分别上升至２．４和２．９倍,说明高温胁迫对ＰＳⅡ中心除了起瞬时钝化作用外,还存在一个间接的较为缓慢的持续钝化作用。     

NaCl胁迫对PSII光能利用和耗散的影响

用荧光动力学的方法研究了不同浓度的ＮａＣｌ 处理对ＰＳＩＩ光能利用和耗散的影响。结果表明,在较低的光强下,与对照、１００ｍ ｍｏｌ／Ｌ 和２００ｍ ｍｏｌ／Ｌ ＮａＣｌ 处理相比,经３００ｍ ｍｏｌ／Ｌ 和４００ｍ ｍｏｌ／Ｌ ＮａＣｌ 处理的小麦,其荧光光化学淬灭效率较低,荧光非光化学淬灭效率较高,Ｆｏ 淬灭系数较大,ＱＢ － 非还原性ＰＳＩＩ反应中心含量较大; 而在较高光强下, 其荧光非光化学淬灭效率和Ｆｏ 淬灭系数则相对较低。     

Genetic analysis of inbreeding depression in plus tree 850.55 of Pinus radiata D. Don. I. Genetic map with distorted markers

 A genetic map of Pinus radiata plus tree 850.55 was constructed using megagametophytes of S₁ seeds. The map contained 19 linkage groups, with 168 RAPD and four microsatellite markers. The total map length was 1116.7 cM (Kosambi’s function) and was estimated to cover 56% of the genome. Of the 172 markers, 59 (34%) were distorted from the expected 1 : 1 ratio in megagametophytes (P<0.05). We show that if the distortion is caused by a single viability gene or by sampling error, the estimate of recombination frequency in megagametophytes of selfed seeds would not be affected. Received: 20 April 1998 / Accepted: 13 July 1998     

甘蔗抗逆细胞系选择及其生化特性的研究

利用脯氨酸类似物羟脯氨酸(Hyp)的生长抑制作用,筛选出抗Hyp的甘蔗(Saccha-rum sinensis Roxb)细胞变异系R932。抗性系体内游离脯氨酸含量超常积累(×3．2)。而且其体内脯氨酸合成途径中的关键酶γ－谷氨酸激酶对脯氨酸的反馈抑制较不敏感。R932抗PEG和低温能力较供体加强。实验结果表明γ－谷氨酸激酶特性的变化可能导致细胞内脯氨酸的过量积累,脯氨酸的过量积累有利于植物细胞对抗恶劣环境。     

Graphene for improved femtosecond laser based pluripotent stem cell transfection

Pluripotent stem cells are hugely attractive in the tissue engineering research field as they can self‐renew and be selectively differentiated into various cell types. For stem cell and tissue engineering research it is important to develop new, biocompatible scaffold materials and graphene has emerged as a promising material in this area as it does not compromise cell proliferation and accelerates specific cell differentiation. Previous studies have shown a non‐invasive optical technique for mouse embryonic stem (mES) cell differentiation and transfection using femtosecond (fs) laser pulses. To investigate cellular responses to the influence of graphene and laser irradiation, here we present for the first time a study of mES cell fs laser transfection on graphene coated substrates. First we studied the impact of graphene on Chinese Hamster Ovary (CHO‐K1) cell viability and cell cytotoxicity in the absence of laser exposure. These were tested via evaluating the mitochondrial activity through adenosine triphosphates (ATP) luminescence and breakages on the cell plasma membrane assessed using cytosolic lactate dehydrogenase (LDH) screening. Secondly, the effects of fs laser irradiation on cell viability and cytotoxicity at 1064 and 532 nm for cells plated and grown on graphene and pure glass were assessed. Finally, optical transfection of CHO‐K1 and mES cells was performed on graphene coated versus plain glass substrates. Our results show graphene stimulated cell viability whilst triggering a mild release of intracellular LDH. We also observed that compared to pure glass substrates; laser irradiation at 1064 nm on graphene plates was less cytotoxic. Finally, in mES cells efficient optical transfection at 1064 (82%) and 532 (25%) nm was obtained due to the presence of a graphene support as compared to pristine glass. Here we hypothesize an up‐regulation of cell adhesion promoting peptides or laminin‐related receptors of the extracellular matrix (ECM) in cell samples grown and irradiated on graphene substrates. By bringing together advances in optics and nanomaterial sciences we demonstrate pathways for enhancement of pluripotent stem cell biology. (© 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Global stability of Gause-type predator-prey systems

In this paper, we present some global stability results obtained from comparison analysis, Bendixson-Dulac criterion or limit cycle stability analysis for the general Gause-type predator-type systems.Research supported in part by a FGIA grant from the Arizona State University Research Fund AMS (MOS) subject classifications. Primary 34C05; secondary 34C25, 92A15.