黑粉虫与黄粉虫幼虫肠道细菌的比较

在黑粉虫和黄粉虫肠道中分别分离获得5株细菌,对其菌体形态、培养性状、染色反应、生理生化反应等进行了系统研究。鉴定结果表明,黑粉虫的5个细菌菌株分别属于金杆菌属(Aureobacterium)、李斯特氏菌属(Listeria)、微杆菌属(M i-crobacterium)、莫拉氏菌属(M oraxella)、短小杆菌属(Curtobacterium);黄粉虫的5个细菌菌株分别属于金杆菌属(Aureobacte-rium)、球形芽孢杆菌(Bacillus sphaericus)、微杆菌属(M icrobacterium)、巨大芽孢杆菌(B.m egaterium)、短小杆菌属(Curtobac-terium)。金杆菌属(Aureobacterium)、微杆菌属(M icrobacterium)和短小杆菌属(Curtobacterium)均在2种昆虫肠道中出现。     

黄粉虫不同虫态肠道细菌分离及鉴定

目的研究黄粉虫肠道细菌的类群与其取食的关系,为进一步开发利用提供理论依据。方法从人工饲养的黄粉虫幼虫、蛹和成虫肠道环境中分离纯化获得9个细菌菌株,对其菌体形态、染色反应、培养性状、生理生化反应进行系统研究。结果研究结果表明,上述9个细菌菌株分别属于放线杆菌属（Actunobacillus）、丙酸杆菌属（Propionibacterium）、柠檬酸杆菌属（Citrobacter）、沙雷菌属（Serratia）、芽胞杆菌属（Bacillus）、皮杆菌属（Dermabacter）、短状杆菌属（Brachybacterium）、棍状杆菌属（Clavibacter）和微小杆菌属（Exiguobcacterium）。结论通过对黄粉虫不同虫态即幼虫、蛹和成虫肠道细菌分离,其细菌种类存在一定差别。     

暗黑鳃金龟甲幼虫肠道细菌分离及鉴定

目的从微生态学角度研究暗黑鳃金龟甲幼虫营养生理活动,探讨其肠道菌群的构成,为其资源开发及生物防治提供理论依据。方法按传统分离方法,从暗黑鳃金龟甲幼虫肠道环境中分离纯化获得10个细菌菌株,对其菌体形态、染色反应、培养性状、生理生化反应进行了系统研究。结果研究结果表明,上述10个细菌菌株分别属于鲁氏耶尔森菌（Yersinia．ruckeri）、侧胞芽胞杆菌（Bacilluslaterosporus）、坚强芽胞杆菌（Bacillus．firmus）、放线杆菌属（Actinobacillus）、飞虫杀雄菌（Arsenophonusllasoniae）、不动杆菌属（Acinetobacter）、气单胞菌Aeromonas）、沙门菌属（Sal—moneUa）、短芽胞杆菌（Bacillusbrevis）、变形菌属（Proteus）。结论通过对暗黑鳃金龟甲幼虫肠道细菌的鉴定,其肠道细菌在培养性状、生理性状、生理生化测定等方面存在较多差异。     

栎黄掌舟蛾幼虫肠道好氧菌群分析及产纤维素酶菌的筛选

栎黄掌舟蛾Phalera assimilis是柞树主要叶部害虫之一。本研究以栎黄掌舟蛾幼虫为材料,从幼虫肠道中分离出好氧细菌23株,通过对16S r DNA扩增产物ARDRA分析后,代表性菌株测序结果表明,23株肠道好氧细菌分别属于葡萄球菌属Staphylococcus sp.、短小杆菌属Curtobacterium sp.、赖氨酸芽孢杆菌属Lysinibacillus sp.、肠球菌属Enterococcus sp.和阿特拉津降解菌属Arthrobacter sp.5个属的细菌,其中,以葡萄球菌属及短小杆菌属细菌种类最多。通过筛选培养基从23株菌中筛选出产纤维素酶菌6株。本研究可为深入了解栎黄掌舟蛾肠道菌群结构、寻找产纤维素酶菌及新的微生物资源等奠定了理论基础。     

菜青虫幼虫肠道细菌的分离及鉴定

目的为深入研究菜青虫肠道的营养生理,分析其取食消化机制,对菜青虫肠道细菌进行了研究。方法从自然种群的菜青虫肠道环境中按传统分离、纯化、培养,获得细菌5个菌株,对其茵体形态、染色反应、培养性状、生理生化反应进行了系统研究。结果鉴定结果l号菌株为李斯特菌属（Listeria）,2号菌株为皮杆菌属（Dermabacter）,3号菌株为丙酸杆菌属（Propionibacterium）,4号菌株为沙雷菌属（Serratia）,5号菌株为短状杆菌属（Brachybacterium）。结论在菜青虫肠道环境中分离出5个菌株,鉴定出分类地位。其菌株之间的数量具有明显差异,以皮杆菌属数量最多（2×10^8）,需进一步研究该菌的功能及其在菜青虫肠道中的作用。     

窗胸萤肠道细菌分离及鉴定研究

从窗胸萤的5龄幼虫中分离纯化获得10个细菌菌株,并对其菌体形态、染色反应、培养性状、生理生化性状进行了系统研究。鉴定结果表明,上述10个细菌菌株分别属于埃希氏菌属(Escherichia)、金色单胞菌属(Chryseomonas)、放线杆菌属(Actinobacillus)、摩根氏菌属(Morganella)、李斯特菌属(Listeria)、金杆菌属(Aureobacterium)、微杆菌属(Microbacterium)、地杆菌属(Terrabacter)、芽孢杆菌属(Bacillus)和黄杆菌属(Flavibacterium)。     

不同食料植物对东亚飞蝗肠道细菌状况的影响

目的比较在相同的环境条件下不同食料植物对东亚飞蝗肠道细菌状况的影响。方法以墨西哥玉米、野生马唐为食料植物饲喂东亚飞蝗,在其成虫肠道内和粪沙中分离纯化细菌,获得22株菌株,分别对其培养性状、菌体形态、染色反应和生理生化性状进行系统研究。结果上述22个菌株分别属于稀有杆菌属（Rarobact-er）、短状杆菌属（Brachybacterium）、棒杆菌属（Corynebacterium）、棍状菌属（Clavibacter）、葡萄球菌属（Staphylococ-cus）、丙酸杆菌属（Propionibacterium）、埃希菌属（Eschrichia）、气微杆菌属（Aercmicrobium）、沙雷菌属（Serratia）、克雷伯菌属（Klebsiella）、沙门菌属（Salmonella）、志贺菌属（Shigella）、口腔球菌属（Stomatococcus）、短杆菌属（Brevibacteri-um）、地杆菌属（Terrbacter）、微小杆菌属（Exiguobacterium）、皮杆菌属（Dermabacter）、短小杆菌属（Curtobacterium）、纤维单胞菌属（Cellulomonas）、微杆菌属（Microbacterium）、乳杆菌属（Lactobacillus）和凝结芽胞杆菌属（Bacilluscoag-ulans）。结论不同食料植物对东亚飞蝗肠道细菌种类和数量有很大的影响。     

六斑异瓢虫成虫肠道细菌分离及鉴定研究

目的通过对肠道菌群的研究,探讨其营养生理,进而改善和研制人工饲料,提高六斑异瓢虫的抗逆力和成活率。方法按照传统的培养分离方法从六斑异瓢虫雌成虫肠道消化道内分离纯化获得5个不同菌株,分别对其培养性状、菌体形态、染色反应、生理生化性状进行了系统研究。结果上述5个细菌菌株分别属于地杆菌属（Terrabacter）、李斯特菌属（Listeria）、短小杆菌属（Curtobacterium）、纤维单胞菌属（Cellulomonas）和皮杆菌属（Demabacter）。结论六斑异瓢虫的菌群种类与其生活习性有关,为进一步研究适合六斑异瓢虫生长和繁殖的人工饲料提供数据参考。     

白星花金龟成虫肠道细菌的分离鉴定

目的自星花金龟是我国北方常见腐食性昆虫,为了利用其腐食性行为转化处理有机垃圾、畜禽粪便及农作物秸杆等农业有机废弃物资源,并探索其中肠消化的微生态机制,而对其肠道细菌进行系统研究。方法从白星花金龟成虫肠道中无菌操作分离获得5株细菌,对其菌体形态、培养性状、染色反应、生理生化反应等进行鉴定及数量测定。结果白星花金龟成虫肠道的5个细菌菌株分别属于气球菌属（Aerococcus）、短状杆菌属（Brachybacterium）、棍状杆菌属（Clavibacter）、李斯特菌属（Listeria）、皮杆菌属（Dermabacter）,以皮杆菌属和棍状杆菌属数量最多,分别为1．3×10^7和1．0×10^7;其次为短状杆菌属和气球菌属,分别为8×10^6和5×10^6;李斯特菌属数量最少,为7×10^5。结论各菌株之间细菌数量存在明显差异,以皮杆菌属细菌数量最多,分离未获得真菌和放线菌。     

东亚飞蝗肠道细菌的研究

目的从微生态学角度研究东亚飞蝗的营养生理活动。方法从东亚飞蝗自然种群的雌、雄成虫肠道环境中分离、纯化、培养,获得细菌16个属的菌株,对菌体形态、染色反应、培养性状、生理生化反应进行系统研究。结果上述16个细菌菌株分别属于沙雷菌属(Serratia)、短状杆菌属(Brachybacterium)、预研菌属(Yokenella)、肠杆菌属(Penterobacter)、微杆菌属(Microbacterium)、柠檬酸杆菌属(Citrobacter)、类芽胞杆菌属(Paenibacillus)、沙门菌属(Salmonella)、棍状杆菌属(Clavibacter)、放线杆菌属(Actinobacillus)、米勒菌属(Moelleralla)、不动杆菌属(Acinetobacter)、埃希菌属(Escherichia)、葡萄球菌属(Staphylococcus)、克吕沃尔菌属(Kluyvera)、克雷伯菌属(Kleb-siella)。结论东亚飞蝗雌性成虫肠道环境细菌种类为12个,雄性为10个,其中6个菌株相同;数量之间存在明显差异。     

Phylogenetic analysis of the coryneform bacteria by 5S rRNA sequences.

Nucleotide sequences of 5S rRNAs from 11 coryneform bacteria were determined. These were the type strains of Corynebacterium glutamicum, Corynebacterium xerosis, Brevibacterium linens, Arthrobacter globiformis, Cellulomonas biazotea, Aureobacterium testaceum, Curtobacterium citreum, Pimelobacter simplex, and Caseobacter polymorphus and representative strains of "Corynebacterium aquaticum" and Corynebacterium xerosis. A phylogenetic tree constructed from the sequences of these bacteria and published sequences indicated that the coryneform bacteria consist of a distinct eubacterial branch together with Streptomyces and Micrococcus spp. These bacteria could be further divided into four subgroups.     

Further evidence for the phylogenetic coherence of actinomycetes with Group B-peptidoglycan and evidence for the phylogenetic intermixing of the genera Microbacterium and Aureobacterium as determined by 16S rDNA analysis

Abstract A 16S rDNA study was performed on at least two species, including the type strain of the type species, of each genus described to possess peptidoglycan of Group B. Analyses confirm that these actinomycetes form a phylogenetically coherent cluster within the arthrobacteria subline of descent. While members of the genera Agromyces, Clavibacter, Curtobacterium and Rathayibacter appear to be phylogenetically coherent, members of Microbacterium and Aureobacterium do not cluster according to their taxonomic affiliation but form one large cluster in which species of both genera are intermixed. Species with no taxonomic standing, i.e. "Corynebacterium aquaticum" , and "Brevibacterium helvolum" form three separate sublines of descent and can be considered nuclei of future novel genera.     

Catenarin Production by Isolates of Pyrenophora tritici-repentis (Died.) Drechsler and its Antimicrobial Activity

A total of 88 Pyrenophora tritici‐repentis (Died.) Drechsler isolates from different hosts and localities were screened for catenarin production using thin layer chromatography. Catenarin was detected in 29% of the tested strains. The level of this compound ranged from 2 to 400 ppm and was especially high in case of fungus variants unable to biosynthesize melanins. The extracted pigment exhibited antibiotic properties against Gram‐positive bacteria (Aureobacterium liquefaciens, Arthrobacter globiformis, Bacillus brevis, B. circulans, B. subtilis and Curtobacterium plantarum). Catenarin also inhibited the growth of fungi accompanying P. tritici‐repentis during the saprophytic phase of development. The most sensitive species was Epicoccum nigrum, whose growth was inhibited up to 90%.     

Polyphosphate-dependent enzymes in some coryneform bacteria isolated from sewage sludge

Abstract Eleven isolates obtained from a laboratory sewage treatment plant, most of them presumptively assigned to the coryneform genera Curtobacterium and Aureobacterium were studied for the presence of intracellular polyphosphates and polyphosphate dependent enzymes. All isolates stored polyphosphates and showed adenylate kinase activities ranging from 64 to 815 mU mg⁻¹. Polyphosphate:AMP phosphotransferase could only be detected in one isolate. Three isolates showed a polyphosphate kinase activity also in minor amounts from 15 to 17 mU mg⁻¹. A polyphosphate dependent NAD or 3-phosphoglycerate kinase could not be detected. Polyphosphate glucokinase activity was measured in cell-free extracts of nine isolates ranging from 2 to 376 mU mg⁻¹. Three isolates showed in addition to the polyphosphate glucokinase, a glucose-6-phosphate-dependent NAD kinase. For the regeneration of NADP from NAD and polyphosphate, this enzyme system may give the isolates a distinct competitive advantage, especially for anabolic processes. The polyphosphate-dependent enzymes reported here may play an additional role in the complex process of 'biological' phosphate removal from wastewater.     

Nucleic acid hybridization studies on Microbacterium, Curtobacterium, Agromyces and related taxa

Thirty strains of Agromyces, Arthrobacter, Curtobacterium, Brevibacterium, Corynebacterium and Microbacterium, exhibiting the rare peptidoglycan of group B, were subjected to extensive nucleic acid hybridization studies. The DNA homology values indicate that Corynebacterium insidiosum DSM 20157 is genetically identical with Corynebacterium michiganense DSM 20134. Corynebacterium sepedonicum NCPPB 378 and Corynebacterium nebraskense DSM 20400 are closely related to Corynebacterium michiganense DSM 20134. Corynebacterium betae DSM 20141, Corynebacterium oortii ATCC 25283 and Corynebacterium poinsettiae ATCC 9682 are genetically identical with Corynebacterium flaccumfaciens DSM 20129. In addition, Curtobacterium citreum ATCC 15828, Curtobacterium luteum ATCC 15830 and Curtobacterium pusillum ATCC 19096 share a high degree of relatedness to Corynebacterium flaccumfaciens DSM 20129. All other described species are more distantly related to each other. DNa-rRNA cistron similarity studies reveal that all corynebacterium with a peptidoglycan group B are members of one homogeneous cluster for which the rank of a genus is suggested.     

植物病原棒形细菌的RAPD分析

采用RAPD分析技术对萎蔫短小杆菌落葵致病变种（Curtobacterium flaccumfaciens pv. basellae pv. Nov.）和萎蔫短小杆菌糖甜菜致病变种（Curtobacterium flaccumfaciens pv. beticola pv. Nov.）及植物病原棒形细菌4个属的15个菌株进行分类研究：从50条随机引物中筛选出20条,共产生225条带,多态性条带占804%。遗传相似矩阵及UPGMA聚类分析,表明这两个新致病变种与萎蔫短小杆菌属亲缘关系近,最小相似系数为0.6511;与其他属细菌亲缘关系较远;结合前人研究结果对植物病原棒形细菌新近提出的分类地位的改变进行了探讨。     

Purification and characterization of pyridoxal 4-dehydrogenase from Aureobacterium luteolum

A pyridoxal dehydrogenase was purified to homogeneity from Aureobacterium luteolum, which can use pyridoxine as a carbon and nitrogen source, and characterized. The enzyme was a dimeric protein with a subunit molecular weight of 38,000. It had several properties distinct from those of the partially purified enzyme from Pseudomonas MA-1. The optimum pH (8.0-8.5) was 0.8-1.3 lower than that of the Pseudomonas enzyme. The Aureobacterium enzyme showed much higher and lower affinities for NAD+ (Km, 0.140 +/- 0.008 mM) and pyridoxal (0.473 +/- 0.109 mM), respectively, than those of the Pseudomonas enzyme. The Aureobacterium enzyme could use NADP+ as a substrate: the reactivity was 6.5% of NAD+. The enzyme was much more tolerant to metal-chelating agents. Irreversibility of the enzymatic reaction was shared by the two enzymes. No aldehyde dehydrogenase showed similarity to the amino-terminal amino acid sequence of the enzyme.     

Evidence for a new pathway in the bacterial degradation of 4-fluorobenzoate

Six bacterial strains able to use 4-fluorobenzoic acid as their sole source of carbon and energy were isolated by selective enrichment from various water and soil samples from the Stuttgart area. According to their responses in biochemical and morphological tests, the organisms were assigned to the genera Alcaligenes, Pseudomonas, and Aureobacterium. To elucidate the degradation pathway of 4-fluorobenzoate, metabolic intermediates were identified. Five gram-negative isolates degraded this substrate via 4-fluorocatechol, as described in previous studies. In growth experiments, these strains excreted 50 to 90% of the fluoride from fluorobenzoate. Alcaligenes sp. strains RHO21 and RHO22 used all three isomers of monofluorobenzoate. Alcaligenes sp. strain RHO22 also grew on 4-chlorobenzoate. Aureobacterium sp. strain RHO25 transiently excreted 4-hydroxybenzoate into the culture medium during growth on 4-fluorobenzoate, and stoichiometric amounts of fluoride were released. In cell extracts from this strain, the enzymes for the conversion of 4-fluorobenzoate, 4-hydroxybenzoate, and 3,4-dihydroxybenzoate could be detected. All these enzymes were inducible by 4-fluorobenzoate. These data suggest a new pathway for the degradation of 4-fluorobenzoate by Aureobacterium sp. strain RHO25 via 4-hydroxybenzoate and 3,4-dihydroxybenzoate.     

Evidence for a new pathway in the bacterial degradation of 4-fluorobenzoate.

Six bacterial strains able to use 4-fluorobenzoic acid as their sole source of carbon and energy were isolated by selective enrichment from various water and soil samples from the Stuttgart area. According to their responses in biochemical and morphological tests, the organisms were assigned to the genera Alcaligenes, Pseudomonas, and Aureobacterium. To elucidate the degradation pathway of 4-fluorobenzoate, metabolic intermediates were identified. Five gram-negative isolates degraded this substrate via 4-fluorocatechol, as described in previous studies. In growth experiments, these strains excreted 50 to 90% of the fluoride from fluorobenzoate. Alcaligenes sp. strains RHO21 and RHO22 used all three isomers of monofluorobenzoate. Alcaligenes sp. strain RHO22 also grew on 4-chlorobenzoate. Aureobacterium sp. strain RHO25 transiently excreted 4-hydroxybenzoate into the culture medium during growth on 4-fluorobenzoate, and stoichiometric amounts of fluoride were released. In cell extracts from this strain, the enzymes for the conversion of 4-fluorobenzoate, 4-hydroxybenzoate, and 3,4-dihydroxybenzoate could be detected. All these enzymes were inducible by 4-fluorobenzoate. These data suggest a new pathway for the degradation of 4-fluorobenzoate by Aureobacterium sp. strain RHO25 via 4-hydroxybenzoate and 3,4-dihydroxybenzoate.