羧基酶 的英文怎麼說
中文拼音 [suōjī]-
Based on recent molecular phylogenetic analyses using nucleotide sequences of the encoding the large subunit of ribulose 1, 5 - bisphyosphate carboxylase / oxygenase ( rbcl ), hypodematium should be not included in the athyriaceae, it has closely related to dryopteridaceae. on the other hand, athyriaceae, thelypteridaceae, blechnaceae, onocleaceae and woodisaceae form a large clade, so it may explain that tryon & tryon ( 1982 ) and kramer & kato ( 1990 ) putting it forward as dryopteriaceae s. 1
運用cpdna基因組編碼的磷酸核酮糖羧化酶大亞基( rbcl )的基因序列測定而構建的系統樹,顯示蹄蓋蕨科、金星蕨科、烏毛蕨科以及其他科構成一條與鱗毛蕨科平行的分支,因此可以說明kramer & kato ( 1990 )把蹄蓋蕨科放入廣義的鱗毛蕨科是不合理的。Decarboxylase an enzyme that catalyzes the decarboxylation of carboxylic acids, including the conversion of amino acids to amines
脫羧酶:能夠催化羧酸進行脫羧反應的酶,包括氨基酸轉化為胺的反應。Other : the dyewood is known as the suppression histidine decarboxylase, the catecha phenol - o - methyl shift enzyme action
其它:染料木素有抑制組氨酸脫羧酶,兒茶酚- o -甲基轉移酶作用The association of gene polymorphisms of mgp and alad with lead blood level in children
羧基谷氨酸蛋白和氨基乙酰丙酸脫水酶基因多態性與兒童血鉛的關系Many glycoproteins of lower and higher eucaryotes are attached to the plasma membrane by means of a glycosylphosphatidylinositol ( gpi ). gpi - anchored proteins are synthesized on membrane - bound ribosomes. upon translocation of the pro - protein across the endoplasmic reticulum membrane, gpi : protein transamidase ( gp1t ) recognize and removes the carboxy terminal gpi signal sequence and attaches a gpi molecule to the newly exposed carboxy terminal amino acid
Gpi化前體蛋白在依附於膜的核糖體上合成,當其易位穿過內質網( er )膜后,被gpi :蛋白質轉酰胺基酶( gpit )識別, gpit在移走其羧基端gpi信號序列的同時將gpi分子連接至新生成的氨基酸位點上。- acetolactate decarboxylase are widely found among bacterial strains but not in other groups of organisms. the enzyme has been demonstrated to be effective for removal of acetolactate and widely used in beer product. in this paper, - acetolactate decarboxylase from bacillus subtilis was purifed to homogeneity from cell extract by ammonium sulfate - fractionation, heat treatment, deae - sepharose fast flow column chromatography
本文對來源於枯草芽孢桿菌( bacillussubtilis ) 3226 - 5的-乙酰乳酸脫羧酶經硫酸銨分級沉澱、熱處理、 deae - sepharosefastflow離子交換柱層析等分離純化步驟,得到sds - paeg電泳純,通過n末端氨基酸序列分析驗證酶蛋白的純度。An enzymatic synthesis and composition of oligomers and co - oligomers comprised of. alpha. - hydroxy carboxylic acids and. alpha. - amino acids or peptides is disclosed
一種低聚體和由-羥基羧酸和-氨基酸或肽組成的副低聚體的酶合成成分。The enzyme had its optimum activity at ph 3. 5 and 55 and its km for sodium carboxymethyl cellulose at 50 and ph 5. 0 was 7. 41mg / ml. sacilin was inhibited the enzyme
-葡萄糖苷酶與內切-作用,可加速水解羧甲基纖維素鈉;內切p ?葡聚糖苷酶對葡萄糖苷酶水解水楊素具有抑制作用。3. 2. 1. 4 ) which was prepared by precipitation of the water extract of the culture of aspergillus niger with ammonium sulfate and desalted by sephadex g - 25, and was further fractionated by two steps of deae - toyopearl 650m and one step of poros 20pi chromatography. the other was a p - glucosidase ( ec. 3. 2. 1. 21 ) which was prepared by the above g - 25 fractions and was further fractionated by two steps of deae - toyopearl 650m chromatography. the specific activity of the endoglucanase with sodium carboxymethyl cellulose was estimated to be 433. 38 hj / mg
-葡萄糖苷酶對水楊素的比活力為597 . 12iu mg ,並對其專一,不能水解棉花和羧甲基纖維素鈉;分子量為117 . 5kda ,加dtt後分子量不變;該組分最適ph和溫度分別為4 . 5和70 ,在ph5 . 0 、 50下對水楊素鈉的米氏常數km為3 . 73mg ml ,最大反應速度vm為0 . 088mg葡萄糖( ml ? min ) ;與文獻中從黑麴黴中分離的-葡萄糖苷酶比較后發現,該組分是一個新的-葡萄糖苷酶。The reduced level of cell - free rumen fluid had no significant effect on xylanase production, but had significant effect on the cmcase activity. without cell - free rumen fluid, the high concentration level of yeast extract could improve xylanase and cmcase production. in the third section, crude enzymes produced by anaerobic fungus a4 was extracted, and their characteristics of the crude enzyme was also investigated
與基礎產酶培養基相比,降低培養基中無細胞瘤胃液濃度對厭氧真菌所產木聚糖酶的酶活及比活力無顯著影響( p 0 . 05 ) ,但對其所產的羧甲基纖維素酶的酶活及比活力有顯著影響( p 0 . 05 ) 。Inhibitor of aromatic l amino acid decarboxylase
芳香氨基酸脫羧酶抑制劑As well as in eukaryocyte ( hepg2 and cos - 7 ), then detect their antigenity as a basis study and explore of the choice of immunogen for preventive and therapeutic vaccines of hepatitis b. methods : the gene fragments coding 152aa ( si ) and 124aa ( s2 ) of the carboxyl terminus of hbsag were amplified by pcr from plasmid pecob6 with a pair of primers containing different endonuclease sites and were cloned into multiple cloning sites of plasmid pbks ( + )
為乙型肝炎的預防和治療性疫苗免疫原的選擇進行初步的研究和探討。方法:本研究利用聚合酶鏈反應( pcr ) ,通過設計帶有不同酶切位點的一對引物,從質粒pecob6特異性擴增hbsag蛋白羧基末端152個氨基酸( s1 )和124個氨基酸( s2 )的基因片段,分別將二者克隆到質粒pbks ( + )的多克隆位點,篩選重組克隆。In this study, it has been put forward that taking reactive nanometer magnetic fe304 particles as magnetic nucleus, and the copolymer of styrene ( st ) ? crylic acid ( aa ) as macromolecular shell, we could synthesize, magnetic polymer composite microspheres containing carboxyl groups on their surface, then microspheres are activated by thionylchloride, the surface of such magnetic composite microspheres thus produced had reactive acid chloride groups which then react with the free amino groups of the free soluble enzymes to give peptide bonds ( ? o ? h ?,
本研究首次提出了以納米級磁性fe _ 3o _ 4粒子為核心,苯乙烯( st ) ?丙烯酸( aa )共聚物為高分子殼層,合成了表面帶羧基的磁性高分子復合微球,然後將這種微球用二氯亞碸進行活化處理,在其表面形成了反應性酰氯基團,該基團可以與游離酶的氨基形成肽鍵,從而將游離酶固定化。Effect of medium components on enzyme production and characterization of anaerobic fungal crude enzymes were also investigated. this thesis was described in the following three sections. in the first section, twelve anaerobic fungal strains isolated from rumen and faeces of ruminants were screened for xylanase and cmcase production
本研究從黑白花種公牛、水牛、山羊糞樣及山羊瘤胃內容物中分離到12株厭氧真菌,並對其進行了產高活性羧甲基纖維素酶和木聚糖酶菌株的篩選,同時還就培養基主要組分對厭氧真菌產酶的影響和厭氧真菌的粗酶性質進行了研究。Proteolytic enzymes catalyze oligomerization of the. alpha. - hydroxy carboxylic acid and. alpha. - amino acid
蛋白水解酶催化-羥基羧酸和-氨基酸的低聚化。The mlap was analyzed with bioinformatics software. it has two domains : zincins catalytic domain and c - terminal domain of metalloprotease
該酶含有兩個結構域,分別為zincins催化結構域和金屬蛋白酶羧基端結構域。The genes encoding pyruvate decarboxylase ( pdc ) and alcohol dehydrogenase ii ( adh ii ) were amplified from total dna of zymomonas mobilis by pcr. the genes of adhb andpdc were inserted into expression vector pse380 and then transformed into e. coli dh5a. the recombinant strains were induced to express adh ii and pdc with iptg
本論文以zymomonasmobilisdna為模板, pcr擴增zymomonasmobilis中的乙醇脫氫酶基因( adhb )和丙酮酸脫羧酶基因( pdc ) ,分別構建表達質粒pse - adhb和pse - pdc並在大腸桿菌dh5中表達。A review of physiological and biochemical changes and regulation during flower senescence
羧酸合酶基因參與玫瑰花發育過程中細胞程序化死亡的調控分享友人