黄龙山森林植被地上碳储量时空变化及驱动力

快速准确地估计植被地上碳储量及其动态变化,对评估森林固碳能力具有重要意义。以陕西省黄龙林区森林为研究对象,基于样地实测和卫星遥感数据,建立黄龙山林区植被地上碳储量模型,实现研究区2000-2021年长时间序列的森林植被地上碳储量的反演及时空分异研究。结果表明：（1）黄龙山森林植被地上碳储量平均值总体呈波动上升趋势,碳储量高于全省平均水平。（2）研究区东部、南部、中部及西北部是植被地上碳储量高值分布地区,且呈增加趋势;而东北部、西部和西南部植被地上碳储量较低,且呈减少趋势,研究区22年间森林植被地上部分固碳量增加,生产力提升。（3）年均温、年蒸散发量、年降水量和海拔是2000-2021年影响研究区森林植被地上碳储量空间分异主要因素;任意两个因子间的交互作用对黄龙山森林地上碳储量影响都大于单个因子,表明黄龙山森林植被地上碳储量在不同时间的空间分布受多种因素共同作用。年降水量对其空间分布影响逐渐减小,森林稳定性提高。研究在信息有限的基础上提出了快速估算地区植被地上碳储量的方法,了解了地区森林植被地上碳储量时空分异情况及其驱动因素,为掌握地区植被地上碳储量信息、评估森林固碳能力提供了重要依据。     

基于金属有机框架的固定化酰胺酶制备及催化合成(S)-4-氟苯甘氨酸

以微水溶剂热法快速制备的稳定锆基金属有机框架为载体,戊二醛为交联剂,采用交联法对酰胺酶进行固定化,考察了不同条件对酰胺酶固定化效率的影响.结果 表明,戊二醛浓度为1.0％、交联时间为180 min、载体与酶的质量比为8∶1,固定化效率最佳,固定化酶活力回收率达86.4％,蛋白负载量达115.3 mg/g.固定化酶最适温...     

Improving the productivity of 19,20-epoxy-cytochalasin Q in Xylaria sp. sof11 with culture condition optimization

19,20-Epoxy-cytochalasin Q (B5A) is a cytochalasin with a wide range of biological activities, which can be produced by Xylaria sp. sof11, a strain isolated from the seafloor of the northern South China Sea. Since the low titer of B5A has greatly limited its further studies, we have systematically conducted the fermentative optimization for B5A production in this article. The effects of major medium components, including the carbon and organic nitrogen sources, as well as of the concentration of sea salt, were respectively investigated through single-factor experiments. As a result, sucrose and fish meal were determined to be the key factors affecting the production of B5A. Then three important variables, sucrose, fish meal, and filling volume, were screened out by the Plackett–Burman (PB) design. The optimal level of these variables was further confirmed by response surface analysis. The final formulated medium was set as 35.2 g/L sucrose and 18.0 g/L fish meal, with filling volume of 34.6 mL, which could afford 440.3 mg/L production of B5A, approximately 4.4-fold higher than that in the original medium. The significantly improved productivity of B5A will facilitate the subsequent mechanistic and clinical studies of B5A.     

A Preliminary Genetic Analysis of Complement 3 Gene and Schizophrenia

Complement pathway activation was found to occur frequently in schizophrenia, and complement 3 (C3) plays a major role in this process. Previous studies have provided evidence for the possible role of C3 in the development of schizophrenia. In this study, we hypothesized that the gene encoding C3 (C3) may confer susceptibility to schizophrenia in Han Chinese. We analyzed 7 common single nucleotide polymorphisms (SNPs) of C3 in 647 schizophrenia patients and 687 healthy controls. Peripheral C3 mRNA expression level was measured in 23 drug-naïve patients with schizophrenia and 24 controls. Two SNPs (rs1047286 and rs2250656) that deviated from Hardy-Weinberg equilibrium were excluded for further analysis. Among the remaining 5 SNPs, there was no significant difference in allele and genotype frequencies between the patient and control groups. Logistic regression analysis showed no significant SNP-gender interaction in either dominant model or recessive model. There was no significant difference in the level of peripheral C3 expression between the drug-naïve schizophrenia patients and healthy controls. In conclusion, the results of this study do not support C3 as a major genetic susceptibility factor in schizophrenia. Other factors in AP may have critical roles in schizophrenia and be worthy of further investigation.     

Analysis of Xyloglucan Endotransglycosylase/Hydrolase (XTH) Genes and Diverse Roles of Isoenzymes during Persimmon Fruit Development and Postharvest Softening

Xyloglucan endotransglycosylase/hydrolase (XTH) enzymes have played a role in the remodeling of cell wall hemicelluloses. To investigate the function of XTHs in persimmon (Diospyros kaki L.) fruit development and postharvest softening, five cDNAs (DkXTH1 to DkXTH5), whose putative proteins contained the conserved DEIDFEFLG motif of XTH, were cloned. Real time quantitative PCR analysis revealed that DkXTH1, DkXTH4, and DkXTH5 peaked in immature expanding fruit, and their higher expression was observed along with higher fruit firmness in cold-treated fruit or firmer cultivar fruit during storage. The opposite gene expression patterns were observed in DkXTH2 and DkXTH3, which reached maxima concomitance with pronounced fruit softening. Meanwhile, the xyloglucan endotransglycosylase (XET) enzymes play important roles in both the rapid growth and ripening of persimmon fruit. Furthermore, the recombined DkXTH1 and DkXTH2 proteins showed significant XET activity without any detected XEH activity. However, the XET activity of recombined DkXTH2 protein had a higher affinity for small acceptor molecules than that of recombined DkXTH1 protein. The former might prefer to participate in cell wall restructuring, and the latter is more inclined to participate in cell wall assembly. Besides, DKXTH proteins could function by targeting to the cell wall under regulation of a signal peptide. The data suggested that individual DKXTHs could exhibit different patterns of expression, and the encoded products possessed specific enzymatic properties conferring on their respective functions in growth and postharvest softening of persimmon fruit.     

BSP基因RNA干扰对乳腺癌MDA-MB-231BO细胞生物学特性的影响

旨在研究RNA干扰(RNA interference,RNAi)抑制骨唾液酸蛋白(bone sialoprotein,BSP)基因表达后对人乳腺癌细胞MDA-MB-231BO生物学特性的影响。应用pSilencer5.1-U6Retro构建针对BSP基因的siRNA逆转录病毒重组表达质粒,将重组质粒转染293细胞制备病毒悬液感染MDA-MB-231BO细胞,利用嘌呤霉素筛选抑制BSP表达的乳腺癌细胞。Western blotting检测细胞内BSP蛋白表达,采用MTT法和集落形成试验检测细胞的增殖,流式细胞仪检测细胞周期变化。结果显示,成功构建BSP基因RNAi稳定转染的231BO-BSP27细胞。231BO-BSP27细胞内BSP蛋白表达抑制率为69.3%,与对照组细胞相比,231BO-BSP27细胞的生长速率和克隆形成率明显降低;S期细胞数量明显减少,G0/G1期细胞增多。由此证实,逆转录病毒介导的RNAi能实现BSP基因稳定沉默,从而抑制MDA-MB-231BO细胞的生长和增殖。     

Microbial diversity of a sulfide black smoker in main endeavour hydrothermal vent field,Juan de Fuca Ridge

Submarine hydrothermal vents are among the least-understood habitats on Earth but have been the intense focus of research in the past 30 years. An active hydrothermal sulfide chimney collected from the Dudley site in the Main Endeavour vent Field (MEF) of Juan de Fuca Ridge was investigated using mineralogical and molecular approaches. Mineral analysis indicated that the chimney was composed mainly of Fe-, Zn-and Cu-rich sulfides. According to phylogenetic analysis, within the Crenarchaeota, clones of the order Desulfurococcales predominated, comprising nearly 50% of archaeal clones. Euryarchaeota were composed mainly of clones belonging to Thermococcales and deep-sea hydrothermal vent Euryarchaeota (DHVE), each of which accounted for about 20% of all clones. Thermophilic or hyperthermophilic physiologies were common to the predominant archaeal groups. More than half of bacterial clones belonged to ɛ-Proteobacteria, which confirmed their prevalence in hydrothermal vent environments. Clones of Proteobacteria (γ-, δ-, β-), Cytophaga-Flavobacterium-Bacteroides (CFB) and Deinococcus-Thermus occurred as well. It was remarkable that methanogens and methanotrophs were not detected in our 16S rRNA gene library. Our results indicated that sulfur-related metabolism, which included sulfur-reducing activity carried out by thermophilic archaea and sulfur-oxidizing by mesophilic bacteria, was common and crucial to the vent ecosystem in Dudley hydrothermal site.     

Suspension culture of gametophytes of transgenic kelp in a photobioreactor

Transgenic Laminaria japonica gametophytes producing a recombinant tissue-type plasminogen activator (rtPA) protein, which is an effective third-generation thrombolytic agent for acute myocardial infarction (AMI), were cultured in an illuminated bubble column bioreactor. A maximum final dry cell weight of 1120 mg l⁻¹ was obtained in batch culture with an initial dry cell weight of 126 mg l⁻¹ and with aeration rate of 1.2 l air min⁻¹ l⁻¹ culture, nitrate at 1.5 mM and phosphate at 0.17 mM. The yield of rtPA was 56 μg g⁻¹ dry cell wt. This is the first report regarding cultivation of a transgenic macroalga in a bioreactor.Revisions requested 27 January 2005 and 14 April 2005; Revisions received 6 April 2005 and 17 May 2005