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1.
腈类物降解菌多样性和产腈水合酶研究进展   总被引:1,自引:0,他引:1  
腈水合酶催化反应在有机合成领域已有广泛的应用。作为一类重要的催化剂,腈水合酶可以将腈类物质转化为相应的酰胺。由于这种酶具有固有的立体和区域选择性,在精细化工领域已成为绿色、温和、对同分异构体具有选择性的催化剂。同时腈水合酶在生物修复和环境保护中也起着重要作用。综述了目前国内外腈水合酶的研究进展,包括降解腈类的微生物多样性、腈水合酶的催化特性、产腈水合酶菌株的改造以及腈水合酶相关基因的克隆与研究。对固定化酶和腈水合酶的应用也进行了叙述。  相似文献   

2.
3-氰基吡啶水合酶的纯化及性质   总被引:1,自引:0,他引:1  
马红球菌SHB-121胞内3-氰基吡啶水合酶经硫酸铵分级沉淀、DEAE-cellulose DE52和羟基磷灰石柱层析并经过Sephadex G-25处理,得到了聚丙烯酰胺凝胶电泳均一的3-氰基吡啶水合酶,纯化了31倍。该酶由一条肽链组成,棋 分子量为30kD,等电点4.1,3-氰基吡啶水合酶能催化3-氰基吡啶水合生成尼克酰胺。酶反应最适PH为8.0,最适温度为30℃,Ag^+、Hg^2+、Cu^  相似文献   

3.
《日经生物技术》1999年5月10日第16页报道:美国DowAgroSciences公司5月4日宣布,与丹麦大型食品公司—Danisco公司合作开发油菜。Danisco公司的种子事业子公司—DaniscoSeed公司和Dow公司决定成立合资公司,两个公司各出资50%,进行油菜新品种的开发。除利用在丹麦和加拿大两个公司分别拥有的育种点外,今后还打算在德国和法国建立开发点。决定在北美以Dow公司为中心、在欧洲以Danisco公司为中心进行商品化。Danisco公司除食品、饮料外,还进行食品原料的开发…  相似文献   

4.
以E.coli和耐辐射生球菌(Deinococcusradiodurans)为试材,研究了N^+离子注入对其SOD,CAT和POD活性的影响及共对自由基的清除,结果表明:D.radiodurans经N^+离子注入后SOD和CAT酶活高于E.coli的,而POD酶活不仅很低于E.coli的;随剂量的增大,两者SOD和CAT酶活均为增后减,只是其SOD酶活的变化峰值对应剂量分别为6×10^15N^+/  相似文献   

5.
为从基因水平上改造腈水合酶,进行了诺卡氏菌腈水合酶基因的外源表达研究。在重组大肠杆菌表达系统内,腈水合酶的α亚基几乎不能正常表达,在重组E. coli BL21(DE3) (pET32aNHBAX)中,腈水合酶活性仅为0.04U/mg。构建重组毕赤酵母表达质粒pPIC3.5kNHBAX,采用电穿孔转化法将其转入宿主菌P. pastoris GS115中,经过菌株培养和腈水合酶的诱导表达,筛选获得了优选菌株P. pastoris NH4。对P. pastoris NH4的细胞培养和腈水合酶的诱导表达条件进行优化,结果表明,重组腈水合酶在毕赤酵母中的表达水平可以达到0.52U/mg,但不能稳定积累。  相似文献   

6.
系统感染TMV (tobacco m osaic virus)的番茄(Lycopersicon esculentum Mill.)叶胞外蛋白提取液经冰冻干燥浓缩、- 20℃丙酮沉淀、CM-Sephadex C-25离子交换层析、DEAE-Sephadex A-25离子交换层析和Sephadex G-75凝胶层析纯化,获得PAGE均一的β-1,3-葡聚糖酶.SDS-PAGE证明,它包含分子量为36 kD 和27 kD的两个同工酶.以昆布多糖为底物,酶的最适pH 在4.8—5.2之间,在pH 4—8稳定;酶的最适温度在30—40℃之间,在40℃保温1h 后酶活性不变;Km 值为9.2 m g/m L.在系统感染TMV 的番茄叶胞外蛋白提取液中,有分子量为22 kD、27 kD和36 kD的3个β-1,3-葡聚糖酶同工酶  相似文献   

7.
青海南部七种翠雀属植物的核型   总被引:1,自引:1,他引:0  
报道了采自青海南部7 种翠雀属( Delphinium L.) 植物的染色体数目和核型。大通翠雀花D.pylzowii 的核型公式为2n= 16 = 2m + 4sm + 10st; 毛翠雀花D. trichophorum 的核型公式为2n= 16 = 2m + 4sm + 10st; 蓝白翠雀花D.albocoerulum 的核型公式为2n = 16 = 2m + 4sm(2SAT) + 10st; 囊谦翠雀花D. nangchienense 的核型公式为2n = 16 = 2m + 6sm + 8st; 唐古拉翠雀花 D.tangkulaense 的核型公式为2n = 16 = 2m (2SAT) + 6sm + 8st; 单花翠雀花 D.candelabrum var. monanthum 的核型公式为2n = 16 = 2m + 6sm + 8st; 展毛翠雀花D. kamaoensevar. glabrescens 的核型公式为2n = 16 = 2m + 6sm + 8st; 前5 种植物的染色体数目与核型为首次报道。  相似文献   

8.
氰基耐受型腈水合酶是一类生物催化剂。与普通腈水合酶相比,它能够耐受体系中较高浓度的氰基而不受抑制,从而为α-羟(氨)基酰胺的工业化合成开辟了崭新途径。研究腈水合酶的氰基耐受性机理及提高其耐受能力是目前需要解决的关键问题。综述了腈水合酶受氰基抑制的机制,氰基耐受型腈水合酶的发现以及其在蛋氨酸和2-羟基异丁酰胺生物合成中的应用。同时,对今后氰基耐受型腈水合酶基础、应用研究的思路进行了探讨。  相似文献   

9.
丙烯酰胺是一种重要的酰胺类化合物,其聚合产物——聚丙烯酰胺被广泛应用于三次采油、水处理、造纸、冶金等领域。以腈水合酶为核心的生物催化法,尤其是游离细胞催化法,具有转化效率高、产物纯度高以及环境友好等优点,是目前丙烯酰胺生产的主要方法;而腈水合酶及其生产菌株的性能在丙烯酰胺生产工艺中起着至关重要的作用。分别从细胞层次和酶层次对常用的生产菌株性能改造策略进行了简介,并重点阐述了目前用于腈水合酶生产菌株改造的基因重组策略。最后介绍了腈水合酶和产酶细胞的协同改造策略及改造效果。其中,通过对产腈水合酶红球菌R.ruber TH在酶和细胞层面的协同改造,重组游离细胞TH8实现了工业规模约500g/L高浓丙烯酰胺的三批次水合制备。  相似文献   

10.
梧宁霉素产生菌诱变选育的研究   总被引:3,自引:0,他引:3  
以不吸水链霉菌(Sireptomycesahygroselcns)NS—23为出发菌株。菌种斜面孢子萌动后采用紫外线(UV)、硫酸二乙酯(DES)、秋水仙素及加底物等物理化学因子进行诱变处理,经两代连续处理,从UV、DES的复合处理中选育出一株产素较高的突变株UDA257-C-24,产素效价比出发菌株提高了291.72%  相似文献   

11.
对猪细小病毒(PPV)SD-68株印2基因进行的克隆和序列测定表明:SD-68株VP2基因全长1740bD,编码579个氨基酸残基组成的多肽;PPVSD-68株与Kresse株、SY-99株、NADL-2(5075)株、NADL-2(4973)株、US-1株的VP2基因比较,核苷酸的同源性在99%以上,氨基酸的同源性在96%以上。进化树分析表明SD-68株与kresse株的亲缘关系最近;在决定毒株组织嗜性的关键氨基酸位点上(378,383及436),SD-68株与kresse株的差异最小,据此推测SD-68株的组织嗜性与Kresse株相似,即SD-68株属皮炎型PPV;而比较弱毒株NADL-2、SD-68和强毒株kresse VP2的氨基酸差异后发现,215、378和383可能是决定PPV致病性强弱的关键位点。  相似文献   

12.
对猪细小病毒(PPV)SD-68株NS1基因进行了克隆和序列测定,结果表明SD-68株NS1基因全长1989bp,编码662个氨基酸组成的多肽。该序列与PPV SY-99株、Kresse株、NADL-2(5075)和NADL-2(4973)株的NS1基因比较,核苷酸的同源性分别为99.9%、99.9%、99.7%、98.1%,氨基酸的同源性分别为99.7%、99.5%、99.5%、96.7%。PPV SD-68株与MVM(i)、MEV(Abashiri)、CPV、FPV、BPV3、GPVNSl的进化树分析表明:PPVSD-68株NS1与MVM(i)NS1亲缘关系最近,与BPV3 NS1的亲缘关系最远;在Thr435和Ser473位点PPV SD-68株与MVM(i)完全一致,表明Thr435和Ser473是PPV SD-68株NS1潜在的磷酸化位点。  相似文献   

13.
Tryptophan serves as a precursor for the biosynthesis of alkaloids in the ergot fungus, Claviceps purpurea (Fries) Tulasne, and also is believed to act as an inducer of the enzymes necessary for alkaloid production. The characteristics of the transport system responsible for the accumulation of tryptophan in ergot mycelium were investigated, with the goal of clarifying the complex relationships among tryptophan uptake, size of the free intracellular pool of tryptophan, and alkaloid production. The characteristics of tryptophan uptake were studied by pulse feeding radioactively labeled tryptophan to cultures of Claviceps species, strain SD-58, which represented a variety of ages and nutritional states. Tryptophan accumulation in strain SD-58 is mediated by an energy-requiring system which exhibits specificity for neutral aromatic and aliphatic l-amino acids, is pH and temperature dependent, and shows saturation at high substrate concentrations. Tryptophan transport is a function of the intracellular concentration of free tryptophan, the nitrogen deficiency of the mycelium, the rate of growth, and alkaloid production, which were measured in Claviceps strain SD-58 growth in several culture media, some of which promoted alkaloid production and some of which did not. The results indicate that the initial velocity of tryptophan transport is not directly related to alkaloid production.  相似文献   

14.
为制备高效的葡萄酒乳酸菌发酵剂,以酒酒球菌SD-2a为试验材料,研究了5%、10%不同浓度的乙醇胁迫处理对菌体生长、细胞内MLE活性、冻干存活率及细胞膜脂肪酸组分的影响。试验结果表明乙醇胁迫处理明显降低了菌体的生长速率和生物产量。与对照相比,5%乙醇胁迫处理降低了菌体的冻干存活率,而10%乙醇处理却显著增加了菌体的冻干存活率。细胞膜脂肪酸组分的测定结果表明,前者细胞膜U/S比值为1.12,比对照降低了26.3%,而后者细胞膜U/S比值为2.29,比对照增加了50.6%。故认为酒酒球菌SD-2a为适应不同浓度的乙醇胁迫环境,在细胞膜脂肪酸水平上所采用的机制不同,且菌体的冻干存活率与其细胞膜脂肪酸组分密切相关。  相似文献   

15.
目的:从番茄叶片中筛选具广谱抑真菌活性的拮抗内生细菌,研究其对水稻恶苗病菌的抑制作用。方法:采用对峙培养法筛选拮抗内生细菌,根据菌株形态、生理生化特性结合16S rRNA基因序列分析鉴定菌株;采用硫酸铵沉淀法提取抗菌粗蛋白,研究其对水稻恶苗病菌菌丝生长和孢子萌发的影响。结果:从番茄叶片中筛选到一株抗真菌内生多粘芽孢杆菌(Paenibacillus polymyxa)SD-6,该菌株具有广谱抑菌活性,对供试的13种植物病原真菌均具较强的抑制作用;该菌株产生的抗菌粗蛋白能够显著抑制水稻恶苗病菌菌丝生长和孢子萌发,并能导致萌发孢子畸形和破裂。结论:从番茄叶片中分离到一株能产生抗真菌蛋白并具有广谱高效抑真菌作用的内生多粘芽孢杆菌,该菌株及其抗菌蛋白具有防治水稻恶苗病的潜力。  相似文献   

16.
溶磷真菌的筛选及耐盐特性分析   总被引:1,自引:0,他引:1  
【背景】土壤盐渍化已成为影响土壤质量和作物产量的重要因素之一,利用微生物改良盐渍化土壤是既经济又环保的方法。【目的】从不同土壤样品和生物肥料中筛选溶磷能力较强的真菌并讨论其耐盐能力,为盐渍化土壤改良提供菌种资源。【方法】采用平板培养法筛选有一定溶磷能力的真菌,经ITS序列分析初步确定菌株的分类地位。以溶磷能力为考察指标,以NaCl梯度和磷酸钙梯度为考察因素,分析不同菌株利用无机磷源的能力,以及溶磷能力与pH的关系。【结果】共筛选得到16株具有较强溶磷能力的真菌,其中4株真菌对水稻发芽有显著的促进作用,它们是1株长枝木霉(MF-1)和3株踝节菌属菌株(SD-2、XJ-7和HLJ-3)。菌株SD-2和XJ-7生长的耐盐能力显著好于菌株MF-1和HLJ-3。当NaCl浓度为5%时,菌株XJ-7的溶磷能力最好,溶磷率可达9.50%;当NaCl浓度为1%时,菌株HLJ-3的溶磷能力较好,溶磷率为6.93%;当NaCl浓度为0时,菌株SD-2和MF-1的溶磷能力较强,溶磷率分别为9.07%和3.73%。进一步研究发现踝节菌属真菌的溶磷能力与菌液pH呈显著负相关关系。【结论】筛选获得的4株真菌其溶磷能力在不同盐环境中有显著差异,为今后土壤改良和生物肥料中菌种的选择提供理论依据和试验基础。  相似文献   

17.
An aerobic, Gram-staining negative, non-motile, and rod-shaped bacterial strain, SS011A0-7#2-2T, was isolated from the sediment of South China Sea with the depth of 1,500 m. Optimum growth occurred at pH 8.0, 30 °C, and 6 % (w/v) NaCl. Strain SS011A0-7#2-2T did not synthesize bacteriochlorophyll a or carotenoid, neither possess photosynthesis genes. Its genome DNA G+C content was 67.9 mol%. It contained Q-10 as the predominant ubiquinone and C18:1 ω7c (52.3 %) as the major fatty acid. The major polar lipids were phosphatidylcholine, phosphatidylglycerol, diphosphatidylglycerol, phosphatidylethanolamine, unidentified phospholipid, and unidentified aminolipid. The 16S rRNA gene sequence analysis revealed that it was closely related to Seohaeicola saemankumensis SD-15T, Phaeobacter gallaeciensis BS 107T and Roseovarius pacificus 81-2T in Rhodobacteraceae, with the 16S rRNA gene sequence similarities being 96.5, 95.7, and 95.6 %, respectively. However, the phylogeny of the 16S rRNA gene sequences revealed that strain SS011A0-7#2-2T was a member of the genus Seohaeicola. Strain SS011A0-7#2-2T was moderately halophilic which was different from Seohaeicola saemankumensis SD-15T, and it showed the enzyme activities and carbon source spectrum significantly different from Seohaeicola saemankumensis SD-15T. As its physiological and chemotaxinomic properties were different from those of Seohaeicola saemankumensis SD-15T, strain SS011A0-7#2-2T represents a novel species of the genus Seohaecola. The name Seohaeicola nanhaiensis sp. nov. is proposed, with strain SS011A0-7#2-2T (=LMG 27733T = CGMCC 1.12759T) as the type strain.  相似文献   

18.
Escherichia coli strain KF148(SD-) defective in translation of the uncC gene for the epsilon subunit of H(+)-ATPase could not support growth by oxidative phosphorylation due to lack of F1 binding to Fo (M. Kuki, T. Noumi, M. Maeda, A. Amemura, and M. Futai, 1988, J. Biol. Chem. 263, 17, 437-17, 442). Mutant uncC genes for epsilon subunits lacking different lengths from the amino terminus were constructed and introduced into strain KF148(SD-). F1 with an epsilon subunit lacking the 15 amino-terminal residues could bind to F0 in a functionally competent manner, indicating that these amino acid residues are not absolutely necessary for formation of a functional enzyme. However, mutant F1 in which the epsilon subunit lacked 16 amino-terminal residues showed defective coupling between ATP hydrolysis (synthesis) and H(+)-translocation, although the mutant F1 showed partial binding to Fo. These findings suggest that the epsilon subunit is essential for binding of F1 to F0 and for normal H(+)-translocation. Previously, Kuki et al. (cited above) reported that 60 residues were not necessary for a functional enzyme. However, the mutant with an epsilon subunit lacking 15 residues from the amino terminus and 4 residues from the carboxyl terminus was defective in oxidative phosphorylation, suggesting that both terminal regions affect the conformation of the region essential for a functional enzyme.  相似文献   

19.
Abstract Fatty acids were identified in the submerged mycelium of Claviceps purpurea, Claviceps paspali, Claviceps fusiformis and Claviceps sp. SD-58 by gas chromatography-mass spectrometry (GC-MS) and used for a chemotaxonomical study. A close relatedness was found between Claviceps sp. SD-58 and C. fusiformis . The composition of fatty acids in high-production mutants differed substantially from that of the parent strains. Fatty acid analysis is thus probably only applicable in the taxonomy of non-mutated isolates of Claviceps cultured under standard conditions.  相似文献   

20.
甲烷利用菌培养条件的优化及其初步应用   总被引:1,自引:0,他引:1  
利用统计学实验设计(RSM)对能够利用甲烷的假单胞菌菌株ME16主要培养条件进行了优化。以液体无机盐和甲烷气体作为培养基分别进行了温度、接种量、甲烷含量和培养pH对细菌生长影响的研究,并在此基础上,利用响应面法分析优化了ME16菌株的主要培养条件,得到最佳培养条件为:温度29.4℃,接种量1.8%,甲烷含量25%。采用优化培养条件进行培养,细菌生物量增大0.8倍,达到稳定期的培养时间缩短了50h。该菌株初步应用于甲烷气体的脱除,脱除率达65.7 %,表明该菌株能良好的脱除空气中甲烷。  相似文献   

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