Degradation of pyrimidine bases in Clostridium sticklandii

Resting cells of Clostridium sticklandii took up thymine or uracil, when grown in a medium containing 40 mM serine and 20 mM thymine or uracil. The uptake was much lower, when the cells had been grown in a complex medium. Cell-free extracts from cells grown in the complex medium reduced the two bases to the dihydro compounds and decomposed dihydrothymine to -ureidoisobutyrate, as indicated by thin-layer chromatography. Uptake and degradation were stimulated by both NADH and NADPH. Further breakdown did not occur, as ¹⁴CO₂ was not evolved from C-2-labelled thymine or uracil. The rates of pyrimidine uptake and breakdown of C. sticklandii were lower than those reported for C. sporogenes (Hilton et al., 1975).     

Adenosine deaminase from Azotobacter vinelandii. Purification and properties

Adenosine deaminase (EC 3.5.4.4) was found to occur in the extract of Azotobacter vinelandii, strain 0, and purified by heating at 65°C, fractionation with ammonium sulfate, DEAE-cellulose chromatography and gel filtration on Sephadex G-150. Purified adenosine deaminase was effectively stabilized by the addition of ethylene glycol. The molecular weight of the enzyme was estimated to be 66,000 by gel filtration on Sephadex G-150. The enzyme specifically attacked adenosine and 2-deoxyadenosine to the same extent, and formycin A to a lesser extent. The pH optimum of the enzyme was observed at pH 7.2. Double reciprocal plot of initial velocity versus adenosine concentration was concave upward, and Hill interaction coefficient was calculated to be 1.5, suggesting the allosteric binding of the substrate. ATP inhibited adenosine deaminase in an allosteric manner, whereas other nucleotides were without effect. The physiological significance of the enzyme was discussed in relation to salvage pathway of purine nucleotides.     

Nesting,eggs and larvae of triggerfishes (Balistidae)

Synopsis Triggerfishes construct nests by excavating depressions in sand. Eggs are laid in an adhesive mass and anchored with rubble. A photograph of a newly-hatched embryo is included.     

Microautoradiographic studies on host-parasite interactions II. The exchange of 3H-lysine between Uromyces phaseoli and Phaseolus vulgaris

A new species of anaerobic bacterium that degrades the even-numbered carbon fatty acids, butyrate, caproate and caprylate, to acetate and H₂ and the odd-numbered carbon fatty acids, valerate and heptanoate, to acetate, propionate and H₂ was obtained in coculture with either an H₂-utilizing methanogen or H₂-utilizing desulfovibrio. The organism could be grown only in syntrophic association with the H₂-utilizer and no other energy sources or combination of electron donor and acceptors were utilized. It was a Gram-negative helical rod with 2 to 8 flagella, about 20 nm in diameter, inserted in a linear fashion about 130 nm or more apart along the concave side of the cell. It grew with a generation time of 84 h in co-culture with Methanospirillum hungatii and was present in numbers of at least 4.5×10^-6 per g of anaerobic digestor sludge.     

Branched chain amino acid aminotransferase isoenzymes of Pseudomonas cepacia

Pseudomonas cepacia grew rapidly using a mixture of all three branched chain amino acids as carbon source, but failed to use individual branched chain amino acids as sole carbon source. Extracts of bacteria grown on branched chain amino acids had between 2- and 3-fold higher levels of -ketoglutarate-dependent branched chain amino acid aminotransferase activity than extracts of glucose-grown bacteria. The increase in enzyme activity was due to the presence of a second aminotransferase not detected in extracts of glucose-grown bacteria. The enzyme, which presumably plays a role in branched chain amino acid degradation, had an apparent molecular weight (mol. wt.) of 75,000. The other aminotransferase was formed constitutively and apparently functions in synthesis of branched chain amino acids. It was more stable than the 75,000 mol.wt. enzyme, and was purified to homogeneity and found to be a 180,000 mol.wt. oligomer containing 6 subunits of approximately 30,000 mol.wt. Antiserum prepared against the purified enzyme inhibited its activity but failed to influence the activity of the 75,000 mol.wt. aminotransferase, suggesting that the two isoenzymes are encoded by different genes.     

Synthesis and degradation of proteins during wheat endosperm development

Synthesis of proteins rich in lysine declines progressively with endosperm development and these proteins appear to be degraded preferentially at later stages. The proteolytic enzymes in extracts of endosperms at a late stage of development release considerably more lysine radioactivity from labelled endosperm proteins as compared with the enzymes in endosperms at an early stage.     

雄安新区白洋淀生态属性辨析及生态修复保护研究

湿地是自然界生物多样性最丰富的生态系统之一,与社会发展和人类福祉息息相关。近年来,由于全球气候变化和人类活动的过度干扰,湿地正面临着面积萎缩、功能减弱、多样性降低等诸多问题,湿地退化已经成为制约区域可持续性发展的重大阻碍。伴随着生态文明建设逐渐成为中国特色社会主义建设的重要支柱,湿地生态修复工作得到前所未有的制度保障。深入剖析湿地属性,结合政策保障,有针对性的提出湿地保护与修复的治理措施,对区域的生态环境建设和可持续性发展具有重要意义。选择国家级新区-雄安新区的水命脉-白洋淀湿地为研究对象,在深入剖析其生态属性和已存在的生态问题的基础上,结合生态修复的原则、方法和步骤,提出生态修复与保护的可行性策略。研究结果表明,白洋淀本质是典型的湖泊湿地,同时兼具沼泽湿地特征,由于人类活动的剧烈干扰,白洋淀有向沼泽湿地逆向演替的变化趋势。湿地内存在面积萎缩、水资源量短缺、水环境污染问题突出及生物多样性减少等生态问题。本研究建议:为顺利建设雄安新区,首先,白洋淀湿地在算清"水账"、"污账"和"生态账"的前提下,进一步加强流域水资源调配,科学确定白洋淀湿地最佳水位,恢复淀区水量;其次,通过使用清洁生产技术和限制高排污企业建设等措施,加强污染防治,恢复湿地水质;最后,依据生态承载力理论,划分白洋淀流域的生态功能红线、环境质量红线和资源利用红线等国家生态保护红线体系,为尽快恢复湿地结构与功能提供制度保障。     

喀斯特槽谷区生态退化与修复专题导读

在国家重点研发计划项目——"喀斯特槽谷区土地石漠化过程及综合治理技术研发与示范(2016YFC0502300)"的支持下,经过项目组全体成员三年的共同努力,在喀斯特槽谷区生态退化与修复方面取得了一些重要进展。主要有:(1)2000—2015年槽谷区土壤侵蚀总量逐年减少,年平均侵蚀模数逐年降低,槽谷区植被覆盖明显提高;(2)拉巴豆地埂篱根土复合体不仅能有效提高喀斯特土壤的粒径大小和增强土体的抗剪/冲性能,并且能够利用大气N_2合成植物生长所需的氮肥,从而提高土壤肥力,可望实现石漠化治理中生态效应和经济效应的双赢;(3)喀斯特槽谷区隧道建设改变了地下水流场并降低了地下水位,进而降低了土壤微生物丰度和多样性,而增加了适应干旱的微生物种群,并导致土壤质量的降低;隧道建设加速了坡面产流和土壤流失,加剧了土地石漠化,从而导致生态退化;(4)随着槽谷区退化生态系统的恢复,生态系统的生态服务功能得到提升。     

大熊猫肠道芽孢杆菌的分离鉴定及部分生物学特性

【目的】分析大熊猫肠道中芽孢杆菌的种类、纤维素分解能力、抗微生物作用和常用抗生素药物敏感性。【方法】利用芽孢耐高温特性分离菌株,基于16S r RNA基因序列构建系统发育树,通过测量芽孢杆菌在刚果红纤维素培养基上的分解圈分析其纤维素分解能力,采用牛津杯法测定芽孢杆菌的抑菌能力,结合软件分析抑菌能力和进化树之间的关系,通过PCR调查芽孢杆菌的抗菌肽分布规律,最后通过药敏试验检测芽孢杆菌是否对常用抗生素敏感。【结果】共分离得到21株芽孢杆菌;进化树显示,这些芽孢杆菌分为6个类别(Category);羧甲基纤维素钠水解结果显示,所有菌株均能分解纤维素;大部分芽孢杆菌菌株对3种肠道病原菌有较强的抑制能力,聚类分析表明,菌株的抗菌能力与基于16S r RNA基因的分类有一定的关联性;66.67%(14/21)的菌株中可以检测到2个或3个抗菌肽基因;药敏试验结果显示,菌株整体药物耐受率低,仅为7.54%(19/264),但仍有少数菌株对抗生素耐受。【结论】分离菌株种类丰富,分布平均,且均具有纤维素分解能力。21株菌株都含有抗菌肽基因,代谢产物对3种肠道病原菌具有明显抑制作用。常用抗生素耐受性低,对规范临床用药具有指导性。