生物技术进展
生物技術進展
생물기술진전
2011年
6期
426-431,F0003
,共7页
曹威%周利伟%张伟%张宇宏
曹威%週利偉%張偉%張宇宏
조위%주리위%장위%장우굉
聚半乳糖醛酸酶%果胶酶%青霉菌%包涵体%复性
聚半乳糖醛痠酶%果膠酶%青黴菌%包涵體%複性
취반유당철산매%과효매%청매균%포함체%복성
polygalacturonase%pectinase%Penicillium%inclusion body%renaturation
聚半乳糖醛酸酶属于果胶水解酶类,在食品、饲料、纺织和造纸等工业生产中应用广泛。本研究筛选获得一株能分解果胶的青霉菌Penicilliumsp.FJ2,使用简并引物PCR和TAIL-PCR方法从该菌中克隆得到一个聚半乳糖醛酸酶基因pgp1。pgp1基因全长1225bp,包含2个内含子,其cDNA全长1104bp,编码367个氨基酸和一个终止密码子。将pgp1基因连接pET-30a(+)载体并转化大肠杆菌BL21(DE3),重组蛋白以包涵体形式获得表达。通过尿素溶解和梯度稀释方法对重组蛋白PGP1进行了重折叠复性试验,复性后的PGP1聚半乳糖醛酸酶活力达到12.9U/mL,比活力为5.83U/mg。
聚半乳糖醛痠酶屬于果膠水解酶類,在食品、飼料、紡織和造紙等工業生產中應用廣汎。本研究篩選穫得一株能分解果膠的青黴菌Penicilliumsp.FJ2,使用簡併引物PCR和TAIL-PCR方法從該菌中剋隆得到一箇聚半乳糖醛痠酶基因pgp1。pgp1基因全長1225bp,包含2箇內含子,其cDNA全長1104bp,編碼367箇氨基痠和一箇終止密碼子。將pgp1基因連接pET-30a(+)載體併轉化大腸桿菌BL21(DE3),重組蛋白以包涵體形式穫得錶達。通過尿素溶解和梯度稀釋方法對重組蛋白PGP1進行瞭重摺疊複性試驗,複性後的PGP1聚半乳糖醛痠酶活力達到12.9U/mL,比活力為5.83U/mg。
취반유당철산매속우과효수해매류,재식품、사료、방직화조지등공업생산중응용엄범。본연구사선획득일주능분해과효적청매균Penicilliumsp.FJ2,사용간병인물PCR화TAIL-PCR방법종해균중극륭득도일개취반유당철산매기인pgp1。pgp1기인전장1225bp,포함2개내함자,기cDNA전장1104bp,편마367개안기산화일개종지밀마자。장pgp1기인련접pET-30a(+)재체병전화대장간균BL21(DE3),중조단백이포함체형식획득표체。통과뇨소용해화제도희석방법대중조단백PGP1진행료중절첩복성시험,복성후적PGP1취반유당철산매활력체도12.9U/mL,비활력위5.83U/mg。
Polygalacturonases are a class of pectinase that can hydrolyze pectin, and they are widely used in food, feed, textile and paper industry. A Penicillium sp. FJ2, which produced polygalacturonase, has been screened in this research. In addition, a polygalacturonase gene pgp1 has been cloned using degenerated PCR and TAIL-PCR. Length of the polygalacturonase pgp1 gene and its cDNA are 1 225 bp and 1 104 bp, respectively. The cDNA of pgp1 encodes 367 amino acids and a termination codon. Pgp1 was cloned into pET-30a(+) vector and expressed in Escherichia coli BL21(DE3). The recombinant PGP1 was expressed as inclusion bodies without activity towards polygalacturonic acid. The renaturation of the PGP1 was through with urea resolution and gradient dilution. Polygalacturonase activity of the renatured PGP1 was detected as 12.9 U/mL, and with specific activity of 5.83 U/mg.