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普鲁兰酶基因在解淀粉芽孢杆菌BF7658菌株中的分泌表达 被引量:3

Secreted expression of the pullulanase in Bacillus amyloliquefaciens BF7658
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摘要 根据文献报道的核苷酸序列合成Bacillus deramificans普鲁兰酶成熟肽编码基因BdP。将BdP基因插入芽孢杆菌分泌表达载体pUC980信号肽编码区下游,获得重组质粒pUC980-BdP,重组质粒转化中温a-淀粉酶生产菌解淀粉芽孢杆菌BF7658菌株。摇瓶发酵实验表明,重组转化子发酵液有明显普鲁兰酶酶活,约48 h酶活达到最高水平,为2.8 ASPU/mL。酶学性质分析表明,重组酶最适作用温度约为60℃,最适反应pH为5.0,60℃保温3 h仍保存50%的活性。重组酶性质适合淀粉糖化工艺的要求。 According to the sequence of puUulanase gene from Bacillus deramificans (NCBI accession number: BD140672), the gene encoding mature peptide of pullulanase was synthesized and designated BdP. BdP was inserted into the downstream of the DNA fragment encoding signal peptide of pUC980, a secreting expression vector of Bacillus. The constructed plasmid was designated pUC980-/3dP. Subsequently, pUC980-BdP was introduced into Bacillus arnyloliquefaciens BF7658, an industrial mesophilic amylase producer. Active pullulanase was expressed by recombinant t3. aznyloliquefaciens. Recombinant pullulanase was secreted into medium, the optimal time of pullulanase production was 48 h and the enzymatic activity was 2.8 U/mL. Its optimum pH was 5.0 and its optimum temperature was 60 ℃. More than 50 % of its initial enzymatic activity was still detectable after incubated at 60 ℃ for 3 h. The enzymatic property showed that the recombinant pullulanase could be used in saccharification process of starch .
出处 《工业微生物》 CAS CSCD 2012年第2期18-22,共5页 Industrial Microbiology
基金 国家863高技术研究发展计划(2006AA102307 2006AA020204)
关键词 普鲁兰酶 解淀粉芽孢杆菌 BACILLUS deramificans pullulanase Bacillus amyloliquefaciens Bacillus deramificans
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  • 1Yoon K, Jeong Y C, Ju H K, et al. Identification and antimicrobial activity of phenylacetic acidpreduced by Bacillus licheniformis isolated from fermented soybean[J]. Microbiology, 2004, 48 (1): 312-317.
  • 2Erwin H D, Dobek W, Ludolf G B, et al. Novel methods for genetic trans-formation of natural Bacillus subtilis isolates used to study the regulation of the mycosubtilin and surfactin synthetases[J]. Appl Environ Microbiol, 2007, 73 : 3490 - 3496.
  • 3Xue G P, Jennifer S J, Brian P D. High osmolarity improves the electro -transformation efficiency of the gram - positive bacteria Bacillus subtilis and Bacillus licheniformis[J].J Microbiol Methods, 1999, 34:183 - 191.
  • 4Waldeck J, Rammes H M, Wieland S, et al. Targeted deletion of genes encoding extracellular enzymes in Bacillus licheniformis and the impact on the secretion capability[J]. J Biotechnol, 2007, 130: 124- 132.
  • 5Nahrstedt H, Waldeck J, Grone M, et al. Strain development in Bacillus licheniformis : Construction of biologically contained mutants deficient in sporulation and DNA repair[J]. J Biotedmol, 2005,119: 245-254.
  • 6Chang S, Cohen S. High frequency transformation of Bacillus subtilis proto-plasts by plasmid DNA[J]. Mol C, en Goner, 1979, 168:111 - 115.
  • 7Thome C B, Stull H B. Factors affecting transformation of Bacillus lichenifomis[J]. J Bacteriol, 1966, 91: 1012- 1020.
  • 8Bianca W, Jens W, Susanne W, et al. Generation of readily transformable licheniforrnis mutants [ J ]. Appl Microbiol Biotedmol, 2008, 78: 181 - 188.
  • 9Osbom M J. Structure and biosynthesis of the bacterial cell wall[ J ]. Annual Reviews, 1969, 38:501-538.
  • 10Hancock I C, Baddiley J. Biosynthesis of the wall teichoic acid in Bacillus licheniformis[J]. Biochem J, 1972, 127: 27-37.

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