Different O-glycosylation of respiratory mucin glycopeptides from a patient with cystic fibrosis

The O-linked oligosaccharides from three fractions of highly glycosylated mucin glycopeptides obtained from sputum of a patient with cystic fibrosis were characterized and compared regarding size, composition, sequence and when possible linkage positions. Neutral and sialic acid-containing glycans were permethylated and analyzed by high-temperature GC-MS and MALDI-MS, showing more than 60 different oligosaccharides with a size of up to 15 monosaccharide units. Some of the observed oligosaccharides are novel for respiratory secretions, one being a trifucosylated heptasaccharide with the proposed structure: Fuc-Gal-4(Fuc-3)GlcNAc-(Fuc-)Gal-3GalNAcol. The glycosylation of two of the glycopeptide fractions was similar with regard to the neutral and sialylated oligosaccharides despite their different origins from the sol or gel phase. Analysis of the sulfated oligosaccharides by FAB-MS/MS indicated that the gel fraction contained C-6 linked sulfate groups while the two sol fractions also contained C-3 linked sulfate. The results suggest the presence of different glycosylated mucin domains, probably originating from different mucin glycoforms and/or apoproteins in the airway of cystic fibrosis patients.     

On the question of an electrokinetic requirement for phospholipase C action

The phospholipase C of clostridium welchii (alpha toxin) has an absolute requirement for trace quantities of Ca2+. It attacks pure phosphatidylcholine particles (smectic mesophases) having a close-packed bilayer structure only when their surface zeta potential is made positive by the addition of certain divalent ions (e.g., Ca2+) to the aqueous phase or by the presence of low concentrations of long chain cations to the lipid. Alternatively, if the rotational freedom of individual phospholipid molecules is increased by the insertion of short n-alkanols (e.g., hexanol) into the bilayer or when a monolayer of the substrate at an air/water interface is expended, enzymic hydrolysis can occur without any requirement for a net postive charge on the surface.     

Morphology of the male accessory organs of reproduction of immature fallow deer (Dama dama L.) with particular reference to puberty and antler development

Cutting the suspensory ligament reduced the ovarian content of norepinephrine (NE) to less than half that of controls and only a few blood vessels had perivascular fibers and an occasional nerve remained in the interstitial gland. Cutting the ovarian plexus had a less drastic, but similar effect on the ovarian content of NE and on the pattern of ovarian adrenergic nerves. Cutting both the suspensory ligament and ovarian plexus eliminated visualization of ovarian adrenergic nerves, but some ovarian NE was still measurable. Fluorescence and electron microscopic studies of the suspensory ligament revealed a large adrenergic nerve embedded in smooth muscle of the ligament. The nerve was also acetylcholinesterase-positive. Cutting the celiac plexus or incising a small nerve lateral to the plexus and medial to the origin of the suspensory ligament, had the same effect on the ovarian adrenergic nerves as cutting the suspensory ligament. It is concluded that the extrinsic adrenergic nerves to the rat ovary reach the organ by two routes: one via the nerve in the suspensory ligament (superior ovarian nerve), and one via the traditionally described ovarian plexus along the ovarian artery.     

下一代通信技术对广播电视业务发展的影响(下)

(接上期第43页) 3 下一代通信接入对广播电视业务发展的影响 3.1 突破用户接入的瓶颈 随着宽带业务的发展,网络接入部分(最后1 km)的带宽瓶颈问题显露出来.目前,接入部分两侧都已跨入吉比特级以上的速率,如用户端广泛使用的PC,其内部传送速率已达到32 Gb/s,城域网或长途网的每波长速率也已达到2.5～10 Gb/s,两者都比接入部分高出至少3个数量级.可见,尽快打通接入部分的带宽瓶颈,各种宽带服务与应用才能开展起来,网络容量的潜力才能真正发挥.     

昆钢高炉铁水脱碳实验研究

研究了不同铁矿粉氧化剂以及矿粉加入量、铁水初始成分、铁水温度等因素对铁水碳、硅、锰氧化的影响.实验表明巴西粉与滇滩矿具有较好的脱碳效果,在高炉出铁温度范围内,用巴西粉或滇滩矿加入量为2%时,可平均脱去3.3%的碳、50%的硅和30%的锰.对铁水进行氧化脱碳处理后进行冷却,没有发现片状石墨析出.     

Novel electrically conducting polyheteroarylene azines

Abstracts are not published in this journal This revised version was published online in November 2006 with corrections to the Cover Date.