关于《微生物学通报》专题刊申请的通知

当前,随着生物技术的飞速发展,微生物学涵盖的领域越来越广,交叉学科的研究也越来越受到关注。除了已有的微生物学、病毒学、基因工程、细胞工程、酶工程、发酵工程之外,基因组学、代谢工程、纳米科学、生物炼制、生物质能等也逐步成为微生物学研究的热门领域。为了更加系统、集中地反映各个领域     

《生物学杂志》征稿简则

1、《生物学杂志》是生命科学的综合性学术期刊,主要刊登动物、植物、微生物及生理、生化、遗传、生物技术、生物工程、分子生物学等生命科学领域的学术论文以及大中专院校生物教学等方面的经验介绍。主要栏目有：研究报告、综述与专论、技术方法、教学研究等。对反映国内外最新研究成果的论文、国家级自然科学基金资助的论文、获省、部级以上资助项目的科研成果论文将优先发表。     

第十一届国际化石刺丝胞与多孔类学术研讨会在比利时召开北大核心CSCD

第十一届国际化石刺丝胞与多孔类学术研讨会于2011年8月21—26日在比利时的列日大学召开。全球27个国家将近有100名代表出席会议。除了东道主比利时外,参加会议的有中国、俄罗斯、美国、英国、法国、加拿大、日本、澳大利亚、德国、意大利、荷兰、爱尔兰、西班牙、瑞士、奥地利、波兰、罗马尼亚、爱沙尼亚、     

关于《微生物学通报》专题刊申请的通知

当前,随着生物技术的飞速发展,微生物学涵盖的领域越来越广,交叉学科的研究也越来越受到关注。除了已有的微生物学、病毒学、基因工程、细胞工程、酶工程、发酵工程之外,基因组学、代谢工程、纳米科学、生物炼制、生物质能等也逐步成为微生物学研究的热门领域。为了更加系统、集中地反映各个领域     

关于《微生物学通报》专题刊申请的通知

当前,随着生物技术的飞速发展,微生物学涵盖的领域越来越广,交叉学科的研究也越来越受到关注。除了已有的微生物学、病毒学、基因工程、细胞工程、酶工程、发酵工程之外,基因组学、代谢工程、纳米科学、生物炼制、生物质能等也逐步成为微生物学研究的热门领域。为了更加系统、集中地反映各个领域     

桑粉虱形态研究

研究描述了容易与杨梅粉虱混淆的重要害虫桑粉虱Pealius mori(Takahashi)成虫、卵、1～4龄若虫及蛹的形状、分类特征,包括成虫的体长、体色、触角、单眼、复眼、口器、翅、足及雌雄外生殖器;卵的形状、大小、卵色及卵柄;1～4龄若虫及蛹的形状、大小、体色、体周的刚毛、触角、口器、足、管状孔、盖瓣、舌状器及腹沟等。并比较桑粉虱与杨梅粉虱的主要分类特征。     

微生物生物技术及其产品的市场浅析

微生物生物技术(或称微生物技术)是一门以应用微生物学为主体的综合性技术群,主要包括微生物学、生物化学、遗传学及基因工程、细胞工程、酶工程、发酵工程和生化工程等。从纵向划分,包括研究、发展和生产。利用微生物技术生产的产品包括酒类、调味品、有机溶剂、有机酸、氨基酸、维生素、抗生素、甾体激素、酶制剂、活性肽及蛋白、酵母及其它单细胞蛋白、淀粉糖等。应用范围包括食品、轻工、医药、农业、化工、矿业和环境保护等方面。     

能排除人体毒素的食物

1．黄瓜：黄瓜原产于印度，又叫青瓜、胡瓜、刺瓜等，其性平、味甘，具有明显的清热解毒、生津止渴等功效。黄瓜中富含蛋白质、糖类、维生素B2、维生素C、维生素E、胡萝卜素、尼克酸、钙、磷、铁等营养成分，同时还含有丙醇二酸、葫芦素、柔软的细纤维等成分，是难得的排毒养颜佳品。     

关于《微生物学通报》专题刊申请的通知

当前,随着生物技术的飞速发展,微生物学涵盖的领域越来越广,交叉学科的研究也越来越受到关注。除了已有的微生物学、病毒学、基因工程、细胞工程、酶工程、发酵工程之外,基因组学、代谢工程、纳米     

关于《微生物学通报》专题刊申请的通知

当前,随着生物技术的飞速发展,微生物学涵盖的领域越来越广,交叉学科的研究也越来越受到关注。除了已有的微生物学、病毒学、基因工程、细胞工程、酶工程、发酵工程之外,基因组学、代谢工程、纳米科学、生物炼制、生物质能等也逐步成为微生物学研究的热门领域。为了更加系统、集中地反映各个领域的研究成果,以及该领域学科的热点难点问题,充分发挥《微生物学通报》的学科引领和导向作用,促进学     

应用生物法合成内酯化合物

内酯是广泛存在于自然界中具有生物活性的一类化合物。由于大多数内酯化合物具有手性,用化学方法合成不仅过程复杂,而且产率也不高。利用酶反应的特异性,应用生物法合成内酯化合物具有很好的应用前景,其中包括微生物次生代谢合成内酯,脂肪酸生物转化合成内酯和脂肪酶在有机相中催化羟基脂肪酸形成内酯。本文报道这些领域的进展。     

Applications of cell-free protein synthesis in synthetic biology: Interfacing bio-machinery with synthetic environments

Synthetic biology is built on the synthesis, engineering, and assembly of biological parts. Proteins are the first components considered for the construction of systems with designed biological functions because proteins carry out most of the biological functions and chemical reactions inside cells. Protein synthesis is considered to comprise the most basic levels of the hierarchical structure of synthetic biology. Cell-free protein synthesis has emerged as a powerful technology that can potentially transform the concept of bioprocesses. With the ability to harness the synthetic power of biology without many of the constraints of cell-based systems, cell-free protein synthesis enables the rapid creation of protein molecules from diverse sources of genetic information. Cell-free protein synthesis is virtually free from the intrinsic constraints of cell-based methods and offers greater flexibility in system design and manipulability of biological synthetic machinery. Among its potential applications, cell-free protein synthesis can be combined with various man-made devices for rapid functional analysis of genomic sequences. This review covers recent efforts to integrate cell-free protein synthesis with various reaction devices and analytical platforms.     

Synthesis and biological activities of long chain 2-amino alcohols

This article focuses on the synthesis and the biological activities of long chain amino alcohols. The methods for the synthesis of these sphingosine analogues from various starting materials such as lipidic amino acids, serine, glyceraldehydes, long chain 1,2-diols, are summarized in the first part of the review, followed by a discussion of the biological activities of long chain amino alcohols and the applications for the synthesis of other bioactive compounds.     

3-Deoxy-D-arabino-heptulosonic acid 7-phosphate: chemical synthesis and isolation from Escherichia coli auxotrophs

A new chemical synthesis of 3-deoxy-D-arabino-heptulosonic acid 7-phosphate is described and contrasted to isolation of the same molecule from the growth medium of several different auxotrophic strains of Escherichia coli. The higher yielding chemical synthesis begins with 2-deoxyglucose while the less time-intensive biological approach proceeds directly from glucose. Growth and accumulation aspects of whole cell biological synthesis are discussed along with various aspects of the biological purification protocol. Both approaches can be utilized to produce substantial quantities of methyl (methyl 3-deoxy-D-arabino-heptulopyranosid)onate, a key intermediate for semisynthetic 3-deoxy-D-arabino-heptulosonic acid 7-phosphate and a number of its derivatives.     

Synthesis and biological activities of long chain 2-amino alcohols

Summary This article focuses on the synthesis and the biological activities of long chain amino alcohols. The methods for the synthesis of these sphingosine analogues from various starting materials such as lipidic amino acids, serine, glyceraldehydes, long chain 1,2-diols, are summarized in the first part of the review, followed by a discussion of the biological activities of long chain amino alcohols and the applications for the synthesis of other bioactive compounds.     

Nuclear translocation of estrogen-receptor complex and stimulation of RNA synthesis by estrogens of different biological potencies in the female rat pituitary

Stimulation of RNA synthesis and of nuclear translocation of estrogen-receptor complexes was investigated in isolated nuclei of anterior pituitaries of castrated female rats after injection with estrogens of different biological potencies. The assay system for the estimation of total RNA synthesis was validated and data suggest that incorporation of [3H]UMP into acid-precipitable material is consistent with RNA synthesis. An increase in RNA synthesis was seen 30 min after application of either 17 beta-estradiol, estriol or 1,3-diacetyl-17 alpha-ethinyl-7 alpha-methyl-1,3,5,(10)estratriene-17,3-ol (DMEE). RNA synthesis was maximal 90 min after estrogen application. Thereafter, RNA synthesis decreased slowly and reached pretreatment levels 3, 8 and 30 h after application of estriol, 17 beta-estradiol and the diacetyl derivative of ethinyl-estradiol, respectively. All estrogens were found to stimulate rapidly nuclear translocation of estrogen-receptor complexes. Peak levels of nuclear receptor contents were reached 30 min after administration of estrogens. A concomitant depletion of cytosol receptor levels was noted. Nuclear retention of estrogen-receptor complexes paralelled duration of enhanced RNA synthesis and correlated with biological potencies of the steroids. Data of present experiments combine to suggest that long-term nuclear retention is a requisite for expression of biological activity of estrogens at the anterior pituitary. Furthermore, the degree of biological activity seems to be associated with duration of stimulation of RNA synthesis, amount of estrogen-receptor complexes translocated to the nucleus, and duration of nuclear retention.     

Synthesis and biological evaluation of cepharadiones A and B and related dioxoaporphines

Described herein is the first total synthesis and structural confirmation of cepharadione A, a naturally occurring DNA damaging agent. Also reported is the synthesis of cepharadione B, a closely related natural product, as well as the biological evaluation of both natural products. Finally, the preparation and biological evaluation of novel dioxoaporphine analogues is described.     

基因合成技术研究进展

基因合成是生物学中一项最基本的、最常用的技术.对DNA调控元件、基因、途径乃至整个基因组的合成是验证生物学假设和利用生物学为人类服务的有力工具.合成生物学的快速发展对基因合成能力提出了日益迫切的需求.近年来,基于微芯片基因合成技术取得了很多令人振奋的新进展,正在向着高通量、高保真、自动化的方向发展.文中综述了DNA化学合成和基因组装及相关技术的最新研究进展和发展趋势,这些新技术正在推动着合成生物学向着更高的水平发展.     

Diversity-oriented synthesis: exploring the intersections between chemistry and biology

Diversity-oriented synthesis (DOS) is an emerging field involving the synthesis of combinatorial libraries of diverse small molecules for biological screening. Rather than being directed toward a single biological target, DOS libraries can be used to identify new ligands for a variety of targets. Several different strategies for library design have been developed to target the biologically relevant regions of chemical structure space. DOS has provided powerful probes to investigate biological mechanisms and also served as a new driving force for advancing synthetic organic chemistry.     

Pregna-D'-pentaranes--progestins and antiprogestins: I. Differentiation of biological functions of steroid hormones

The synthesis, modification, structure, and biological activity in vivo of the 16alpha,17alpha-cycloalkanoprogesterone (pregna-D'-pentarane) analogues of progesterone are described. A possibility of separation of their biological functions has been demonstrated. A systematic synthesis of a set of uniform compounds that differ in a limited number of alterable parameters was developed. It resulted in an instrument useful for the investigation of pathways and mechanisms by which the steroid hormones fulfill their biological functions and for the probable discovery of new functions masked by the wide effects of native compounds.