芽胞杆菌分类与应用研究进展

芽胞杆菌是一类产生具有抗逆特性芽胞的重要微生物资源,研究其分类地位对挖掘和利用芽胞杆菌功能菌株具有重要科学意义。基于基因组学的多相分类法,使得芽胞杆菌分类地位更加精确。截至2016年6月,全世界芽胞杆菌种类达813种,来自于5个科,即芽胞杆菌科、脂环酸芽胞杆菌科、类芽胞杆菌科、动球菌科、芽胞乳杆菌科,74个属。中国芽胞杆菌研究从2004年开始发表新种,目前,中国学者发表中国分离的芽胞杆菌新种达176种。本文就当前芽胞杆菌主要分类鉴定方法及应用进展进行了描述,希望为国内外芽胞杆菌同行研究者提供一定的帮助。     

生态制品的冻干及保护剂的应用

生态制品的冻干及保护剂的应用卫生部上海生物制品研究所上海２０００５２姚祖华李亦德生态制品主要由活微生物组成,用于制备生态制品的微生物通常有：双歧杆菌、乳杆菌、肠球菌、酵母菌、大肠杆菌、腊样芽胞杆菌、地衣芽胞杆菌、类杆菌等。生态制品按其剂型可分为液体型...     

乳酸菌遗传育种研究现状

乳酸菌是一大类发酵糖产生大量乳酸的细菌的通称 ,主要包括乳杆菌、双歧杆菌、乳球菌、链球菌、肠球菌、明串珠菌、片球菌、芽胞杆菌等属。乳酸菌在医药、工业、农业等与人类生活密切相关的重要领域有很高的应用价值 ,如乳杆菌、双歧杆菌、嗜热链球菌发酵的酸奶 ,应用于保健食品 ;植物乳杆菌应用于青贮饲料 ;乳杆菌、双歧杆菌等应用于临床医疗。但目前很多菌种都是野生型的 ,其某些性状、功能不太令人满意。因此 ,许多研究者通过微生物遗传育种来改良野生型菌株的某些遗传性状 ,以更适合开发利用其价值。1　传统的乳酸菌菌种改良方法1 1　…     

兔肠道正常微生物群的研究

本研究利用稀释滴种的方法,对健康成年家兔回肠及结肠中消化球菌、韦荣氏球菌、梭状芽胞杆菌、优杆菌、双歧杆菌、乳杆菌、肠球菌、酵母菌和肠杆菌等１０种正常微生物群进行了计数分析,并获得其微生态数值,结果显示：结肠中微生物群的总体平均菌数显著高于小肠（Ｐ＜０．０１）;同一菌种在结肠内容物中的在有数量多于回肠;结肠中韦荣氏球菌、肠杆菌为优势菌群;回肠中双歧杆菌、酵母菌为优势菌群。     

短短芽胞杆菌功能基因的研究及其应用

短短芽胞杆菌分布广泛,并且在不同生长阶段,菌落形态也有所不同。目前已经完成2株短短芽胞杆菌的全基因组测序,但只对短短芽胞杆菌部分基因的功能进行了研究,如编码二硫化物氧化还原酶的基因bdb、α-乙酰乳酸脱羧酶的基因aldB、耐碱性木聚糖酶xylB基因和细胞壁的合成基因等,特别是具有抗菌活性的短杆菌酪肽的合成过程及所需酶的基因均有研究。短短芽胞杆菌在生物防治、作为分泌表达外源蛋白的宿主及环境治理等领域有广泛应用前景。     

一株替代粪肠球菌的 生产用芽胞杆菌筛选及其性质

摘要：目的 筛选1株能够产业化、替代粪肠球菌的芽胞杆菌。方法 从健康鸡、鸭、仔猪的粪便与肠道内容物中筛选,采用选择性培养基和耐酸耐胆盐发酵,通过耐人工肠液和人工胃液试验与粪肠球菌比较得到1株产酸能力较好的替代粪肠球菌的芽胞杆菌,并对其性质进行研究。结果 所筛选的芽胞杆菌（GY0520）对人工胃液、人工肠液有很好耐受性,90 ℃水浴15 min存活率为97%,能够产生大量有机酸,有利于提高动物机体的抗病能力及改善其生理性能,但对抗生素有一定的敏感性,不能配伍使用。结论 所筛选的芽胞杆菌能够替代粪肠球菌用于生产,为养殖业的微生态产品提高稳定性提供参考。     

微生物对植物修复重金属污染土壤的促进效果

以印度芥菜作为超富集植物,通过盆栽试验研究了巨大芽胞杆菌和胶质芽胞杆菌的混合微生物制剂、黑曲霉30177发酵液对植物修复Cd、Pb、Zn污染土壤的作用.结果表明：巨大芽胞杆菌和胶质芽胞杆菌的混合微生物制剂不仅可以促进超富集植物的生长,增强超富集植物对土壤Cd、Pb、Zn的吸收,而且大幅度提高了植物的修复效率,在添加外源可溶性Cd、Pb、Zn的污染土壤上,可分别使印度芥菜提取量(以植物干质量计)提高1.18、1.54和0.85倍,在添加底泥Cd、Pb、Zn污染的土壤上,可分别使印度芥菜提取量提高4.00、0.64和0.65倍,在底泥污染的土壤上的促进效果明显强于外源添加污染的土壤.黑曲霉30177发酵液能显著促进印度芥菜对土壤Cd、Pb、Zn的吸收,在添加外源可溶性Cd、Pb、Zn的污染土壤上,印度芥菜地上部Cd、Pb、Zn的吸收量分别比对照提高了88.82%、129.04%和16.80%;在添加底泥Cd、Pb、Zn污染的土壤上,可分别比对照提高78.95%、113.63%和33.85%;但它可导致印度芥菜生物量的大幅度降低,起不到提高植物修复提取量的效果.经反相高效液相色谱初步分析发现,胶质芽胞杆菌、巨大芽胞杆菌发酵液中含有草酸、柠檬酸等有机酸,有机酸对重金属有一定的溶解作用,从而提高了重金属的生物有效性.     

芽胞杆菌对鱼池微生物群落代谢功能的影响

利用Biotog平板,以施用与不施用芽胞杆菌的鱼塘为研究对象,研究鱼塘水体与表泥不同空间的微生物群落代谢功能的差异。结果表明：芽胞杆菌提高了水体微生物群落代谢的平均活性,及对氨基酸类、胺类、羧酸类、聚合物及其它类碳源的利用能力,提高了水体微生物群落代谢的多样性（Shannon均度、Simpson指数、McIntosh均度差异显著）;两池表泥微生物群落代谢平均活性差异较小,对同一碳源的利用差异不大,芽胞杆菌显著提高了表泥的Simpson指数,但表泥的McIntosh指数显著低于对照池。总体而言,鱼塘施用芽胞杆菌,水体微生物群落代谢功能所受的影响大过表泥,芽胞杆菌通过提高水体微生物群落代谢活性,提高了水体微生物对有机污染物的降解能力,以此改善池塘的生态环境。     

静态强磁场对枯草芽胞杆菌的影响研究

目的:研究静态强磁场下微生物的生物学效应.方法:以超导磁体产生的静态强磁场为基础,枯草芽孢杆菌为模式生物,通过测定生长曲线、芽胞生成率、蛋白酶表达量、蛋白酶活力等研究静态强磁场条件下微生物性状的变化.结果:强磁场可以影响枯草芽胞杆菌的芽胞形成速率,抑制营养体的死亡;测定菌体生长过程中蛋白酶的含量以及碱性蛋白酶和中性蛋白酶的酶活力,发现磁场处理前后蛋白酶的含量没有发生显著性变化,处理组碱性蛋白酶的酶活力明显高于对照组,而中性蛋白酶酶活力则低于对照组.结论:强磁场可以延长枯草芽孢杆菌的世代周期,降低菌体死亡率,对细菌酶活性的影响因酶的种类不同而异.     

胶质类芽胞杆菌PCR快速检测方法

摘要:【目的】胶质类芽胞杆菌(Paenibacillus mucilaginosus) 是微生物肥料广泛应用的功能菌种之一,筛选并鉴定其特异性引物,建立该菌种快速检测方法,对微生物肥料产品检测和评价至关重要。【方法】本文筛选了胶质类芽胞杆菌基因间的一段非编码序列作为特异性引物(orf06701-F:5'-ATGGAGGAAACATGGGGTGA-3'/orf06701-R: 5'-TCAGGAATGAAGGCCCCCTT-3'),通过PCR 反应条件/ 体系的优化、特异性及灵敏度检测,建立了胶质类芽胞杆菌     

BMP9-initiated osteogenic/odontogenic differentiation of mouse tooth germ mesenchymal cells (TGMCS) requires Wnt/β-catenin signalling activity

Teeth arise from the tooth germ through sequential and reciprocal interactions between immature epithelium and mesenchyme during development. However, the detailed mechanism underlying tooth development from tooth germ mesenchymal cells (TGMCs) remains to be fully understood. Here, we investigate the role of Wnt/β-catenin signalling in BMP9-induced osteogenic/odontogenic differentiation of TGMCs. We first established the reversibly immortalized TGMCs (iTGMCs) derived from young mouse mandibular molar tooth germs using a retroviral vector expressing SV40 T antigen flanked with the FRT sites. We demonstrated that BMP9 effectively induced expression of osteogenic markers alkaline phosphatase, collagen A1 and osteocalcin in iTGMCs, as well as in vitro matrix mineralization, which could be remarkably blunted by knocking down β-catenin expression. In vivo implantation assay revealed that while BMP9-stimulated iTGMCs induced robust formation of ectopic bone, knocking down β-catenin expression in iTGMCs remarkably diminished BMP9-initiated osteogenic/odontogenic differentiation potential of these cells. Taken together, these discoveries strongly demonstrate that reversibly immortalized iTGMCs retained osteogenic/odontogenic ability upon BMP9 stimulation, but this process required the participation of canonical Wnt signalling both in vitro and in vivo. Therefore, BMP9 has a potential to be applied as an efficacious bio-factor in osteo/odontogenic regeneration and tooth engineering. Furthermore, the iTGMCs may serve as an important resource for translational studies in tooth tissue engineering.     

Identification of Products from Oxidation of Uric Acid Induced by Hydroxyl Radicals

The aim of the present study was to separate and characterise products formed by oxidation of uric acid by hydroxyl radicals with a view to probing for these products in vivo in clinical contexts. Aerated solutions of 200 μM uric acid, or its oxidation products, allantoin or parabanic acid, were exposed to gamma radiolysis, (52.0 Gy/min), as a source of HO- radicals, at pH 3.4 and 7.4. Aliquots were taken every 5 minutes for 20 minutes and oxidation products were separated by HPLC and analysed with a diode array detector. Identities of oxidation products were confirmed on the basis of similarity of retention times and absorbance spectra and peak purity parameters of known standards. Hydroperoxides were measured by tri-iodide formation in the 20 minute sample. Exposure of uric acid to such HO fluxes produced a net loss of the parent compound with formation of a complex mixture of products with allantoin and parabanic acid being the predominant products at pH 3.4. The rate of uric acid degradation at physiological pH was slower and the distribution of oxidation products was different. A small but significant amount of uric acid hydroperoxide was detected at both pHs. A mechanism for uric acid oxidation under these conditions is presented.     

Prevalence and lineages of Listeria monocytogenes in Chinese food products

AIMS: This study was undertaken to investigate the prevalence and lineages of Listeria monocytogenes in different kinds of food products in local Chinese markets. METHODS AND RESULTS: A total of 2686 food samples and 645 water samples were collected and L. monocytogenes was isolated from 2.28% (76 of 3331) of all samples. The prevalence of L. monocytogenes (14 of 290, 4.83%) in raw meat products was significantly higher than that in other raw food products (P < 0.05). Among 844 ready-to-eat (RTE) food samples, 21 samples were positive for L. monocytogenes. RTE packaged food products from two supermarkets had a prevalence ranging from 0.00% to 25.00%. The prevalence of L. monocytogenes in meat products of freshly slaughtered hogs was 0.95% (four of 420), significantly lower than that in raw meat products in the retail markets (P < 0.05). Ten isolates were recovered from 645 water samples, which were collected after hands washing by shopkeepers or waiters. A total of 38 isolates were randomly selected for lineage classification based on the nucleotide variation of actA gene. Eighty percentage of isolates from RTE food products belonged to Lineage II while only 20% belonged to Lineage I. CONCLUSIONS: Food products in Chinese markets are contaminated with L. monocytogenes. Raw meat products have the highest contamination rates among all the raw food samples. RTE food products are more likely to be contaminated with Lineage II strains. SIGNIFICANCE AND IMPACT OF THE STUDY: The data presented here show the main contamination sources of L. monocytogenes in Chinese food products.     

Effects of excretory-secretory products of Echinostoma paraensei larvae on the hematopoietic organ of M-line Biomphalaria glabrata snails.

Responses of the hematopoietic organ (HO) in Biomphalaria glabrata snails to extracts and excretory-secretory (E-S) products of Echinostoma paraensei larvae were studied to understand the HO-activating mechanism. M-line B. glabrata snails were injected with materials from E. paraensei larvae, and the size of the HO was ascertained in histological sections. The size of HO in snails injected with extracts and E-S products from sporocysts and rediae was significantly larger than that in snails injected with culture medium. E-S products of sporocysts were fractionated using ultrafiltration membranes, polyacrylamide gel electrophoresis, and electrophoretic elution. Examination of fractionated E-S products of sporocysts revealed that specific components of E-S products were responsible for HO-stimulating activity.     

Molecular epidemiological survey of Listeria monocytogenes in broilers and poultry products

AIMS: To investigate the prevalence of Listeria monocytogenes in poultry products, and to elucidate whether poultry products may be linked to listeriosis cases. A further goal was to identify contamination routes for L. monocytogenes to broiler carcasses. METHODS AND RESULTS: Poultry products (385 samples) were screened for L. monocytogenes. The recovered isolates and 19 patient isolates were characterized by multilocus enzyme electrophoresis and restriction enzyme analysis. The poultry isolates showed great genetic diversity, but no identical subclones were identified from poultry sources and patients. One slaughterhouse was examined in detail during a 16-month period. The contamination rates increased along the processing line, and one subclone was found during the whole period. Only low prevalence of the bacteria was revealed from broiler faeces. CONCLUSIONS: The prevalence of L. monocytogenes in poultry products was high, but no listeriosis cases was linked to poultry products. Broilers seem to be contaminated during the slaughter process, and specific strains may persist in the processing environment. Broiler faeces does not seem to be an important source of L. monocytogenes in poultry products. SIGNIFICANCE AND IMPACT OF THE STUDY: Preventive measures to avoid contamination of poultry products by L. monocytogenes must be taken in the processing plants.     

Target enzymes on hepatic dysfunction caused by dietary products of lipid peroxidation

Dietary products of lipid peroxidation cause hepatic dysfunction due to decreases in the activities of some hepatic enzymes and to depletion of CoA. An idea about the decreases and depletion is that the enzymes and CoA could be injured directly by the incorporated products in the liver. Their inactivations in vitro were then examined using a reasonable amount of peroxidation products. The hepatic cytosol, microsomes, and mitochondria were incubated with 10, 15, and 20 micrograms/mg protein of peroxidation products, respectively, and changes in the enzymatic activities were monitored. Glucose-6-phosphate dehydrogenase, mitochondrial NAD-dependent aldehyde dehydrogenase, glucokinase, and glyceradehyde phosphate dehydrogenase were inactivated, and the CoA level was decreased, but the other hepatic enzymes were not. Although glyceraldehyde phosphate dehydrogenase was most sensitive to peroxidation products in vitro, the decrease in activity was not detected by the oral dose of secondary products. On the other hand, among the components of peroxidation products, hydroperoxides and polymers are not incorporated in the liver, but decomposed products of low molecular weight are incorporated. Glucokinase among the above enzymes was not inactivated by the low-molecular-weight products. It was therefore concluded that glucose-6-phosphate dehydrogenase, mitochondrial NAD-dependent aldehyde dehydrogenase, and CoA were targets of the direct attack by incorporated components of peroxidation products in the liver.     

生态产品价值实现率评价方法——以丽水市为例

生态产品价值实现是指在维持生态系统稳定性和完整性的前提下，通过合理开发利用生态产品，将其生态价值转化为经济效益的过程。生态产品价值实现机制包含了促进生态产品价值实现的政策、市场和技术机制。生态产品通过各种途径实现的经济价值总和称为生态产品价值实现量。生态产品价值实现量与生态产品总值(GEP)的比值为生态产品价值实现率。评估生态产品价值实现率是评判生态产品价值实现状况的基础，是评估生态产品价值实现机制是否有效运转的重要前提。提出生态产品价值实现率的概念和核算方法，以浙江省丽水市为例，在核算GEP的基础上，评估生态产品价值实现量与实现率来分析丽水市生态产品价值实现状况、问题及影响因素，提出提高生态产品价值实现率的对策建议。研究表明，丽水市2019年GEP为4110.21亿元，生态产品价值实现量为1017.49亿元，生态产品价值实现率为24.76%。丽水生态产品价值实现模式主要有市场交易和政府补偿两种模式。市场交易模式贡献了95.84%的生态产品价值实现量，是目前丽水市最有效的生态产品价值实现模式，但存在价值实现效率不均衡、对于缺乏市场或是市场机制不成熟的生态产品不适用等问题。政府补偿模式贡...     

江苏沿江地区出口产品仓储昆虫群落结构数量特征研究

对江苏沿江地区出口产品仓储昆虫进行调查,分析了5种出口产品仓储昆虫群落的优势种.利用群落物种的丰富度、生态优势度、多样性和均匀度等群落特征指数,研究了5种类型出口产品仓储昆虫群落结构的数量特征,并分析了它们的相似性.通过系统聚类分析将5种群落分为4类,草柳藤制品和羽绒制品仓储昆虫群落同属一类,其它3种产品仓储昆虫群落各属一类.除木制品群落结构相对合理外,其它群落结构都不合理,皮毛制品群落结构尤其不合理.     

Effects of protein deficiency on the metabolism of arachidonic acid by rat pleural polymorphonuclear leukocytes

The effects of protein deficiency on the biosynthesis of metabolites of arachidonic acid by rat pleural polymorphonuclear leukocytes stimulated with calcium ionophore were investigated. The major products of metabolism by lipoxygenase in these cells were leukotriene B4 and 5-hydroxy-6,8,11,14-eicosatetraenoic acid, whereas the major cyclooxygenase products were thromboxane B2 and 12-hydroxy-5,8,10-heptadecatrienoic acid. At high substrate concentrations (100 microM), the formation of all products by polymorphonuclear leukocytes was lower for protein-deficient rats than for controls. Similar results were obtained when products synthesized from endogenous substrate were measured, except that there was no change in the amount of 5-hydroxy-6,8,11,14-eicosatetraenoic acid formed. The biosynthesis of prostaglandins E2 and F2 alpha by homogenates of rat kidney medulla was reduced as a result of protein deficiency. Acetylsalicylic acid inhibited the formation of cyclooxygenase products and stimulated the formation of lipoxygenase products by polymorphonuclear leukocytes. Protein deficiency did not alter the effects of acetylsalicylic acid on the biosynthesis of these products, although at any given concentration the amounts of products formed were less with protein-deficient rats than with rats fed control diets.     

Influence of manufacturing variables on the characteristics and effectiveness of chitosan products. III. Coagulation of cheese whey solids

Ten chitosan products, prepared as described in part I of this study, were evaluated in jar tests that measured their effectiveness for coagulation of suspended solids and removing turbidity from cheese whey. A polynominal regression analysis was found to be useful for determining the optimal effectiveness of each chistosan preparation, and was expressed as the percent reduction on turbidity per unit concentration of chitosan added. The effectiveness of the chitosan products was found to be inversely related to their molecular-weight values. This situation was different from the findings described in part II of this study, in which the filterability of activated sludge was tested. Enzymatic deproteination yielded chitosan products that performed better than those produced by alkali deproteination. Demineralized products were also more effective than those that had not been demineralized. The preparations deacetylated under a nitrogen atmosphere were more effective than those deacetylated in air, but this was shown to be true only for the first 5 min of deacetylation. When deacetylated for 15 min, no differences were noted. In this study, differences in performance between the various products were largely due to the differing dosages required to achieve the maximum reduction in turbidity of cheese whey, while the maximum responses achieved by the various products tested were about the same. A commercial product, which was less effective as a sludge coagulating agent in part II of this study, was more effective for cheese whey coagulation and turbidity removal than the majority of the experimental chitosan preparations tested.