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铜绿假单胞菌algL基因的序列及其藻酸盐裂解酶产物的纯化。

Sequence of the algL gene of Pseudomonas aeruginosa and purification of its alginate lyase product.

作者信息

Boyd A, Ghosh M, May T B, Shinabarger D, Keogh R, Chakrabarty A M

机构信息

Department of Microbiology and Immunology, University of Illinois College of Medicine, Chicago 60612.

出版信息

Gene. 1993 Sep 6;131(1):1-8. doi: 10.1016/0378-1119(93)90662-m.

Abstract

The alginate lyase-encoding gene (algL) of Pseudomonas aeruginosa was localized to a 1.7-kb EcoRI-XbaI fragment within the alginate biosynthetic gene cluster at 34 minutes on the chromosome. The nucleotide sequence of this DNA fragment revealed an ORF encoding a protein of M(r) 40,885 which is transcribed in the same orientation as the other alg genes within the biosynthetic gene cluster. The predicted protein has a potential N-terminal signal peptide which is consistent with its proposed periplasmic location. The AlgL protein was overproduced in Escherichia coli and purified. The purified protein was shown to have alginate lyase activity. In addition, an algL insertion mutant of the mucoid P. aeruginosa 8830 was constructed. This mutant (alm1) had a nonmucoid phenotype due to a polar effect on the transcription of an essential alg gene, algA. Thus, the algL gene is located within a region of the alginate biosynthetic gene cluster that appears to be non-essential for alginate production.

摘要

铜绿假单胞菌的藻酸盐裂解酶编码基因(algL)定位于染色体上34分钟处藻酸盐生物合成基因簇内一个1.7 kb的EcoRI - XbaI片段。该DNA片段的核苷酸序列揭示了一个编码分子量为40,885的蛋白质的开放阅读框,其转录方向与生物合成基因簇内的其他藻基因相同。预测的蛋白质具有潜在的N端信号肽,这与其推测的周质定位一致。AlgL蛋白在大肠杆菌中过量表达并纯化。纯化后的蛋白显示具有藻酸盐裂解酶活性。此外,构建了黏液型铜绿假单胞菌8830的algL插入突变体。该突变体(alm1)由于对必需的藻基因algA的转录产生极性效应而具有非黏液型表型。因此,algL基因位于藻酸盐生物合成基因簇中一个似乎对藻酸盐产生非必需的区域内。

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