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红串红球菌USTB-03对4,6-二甲基二苯并噻吩的脱硫研究 被引量:2

Biodesulfurization of 4, 6-dimethyl Dibenzothiophene by Rhodococcus Erythropolis USTB-03
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摘要 分离出1株能够对4,6-二甲基二苯并噻吩(4,6-DMDBT)进行高效脱硫的微生物菌种,经中国科学院微生物研究所鉴定为红串红球菌USTB-03。研究结果表明,与甘油和乙醇相比,葡萄糖是促进红串红球菌USTB-03生长和提高其脱硫比活性的最好碳源,最高脱硫比活性可达298.1mmol4,6-DMDBT/(kg·h)。在初始pH从4.0到9.0范围内,pH7.0可以使红串红球菌USTB-03保持最大的脱硫比活性。进一步研究显示,红串红球菌USTB-03对4,6-DMDBT脱硫后的最终代谢产物是3,3-二甲基-2-羟基联苯(2-HDMBP),只有C-S键被切断,而C-C键未受到破坏。该脱硫途径类似于二苯并噻吩(DBT)特异性脱硫的途径。 A bacterial strain that has a strong ability in the biodesulfurization of 4,6-dimethyl dibenzothiophene (4,6-DMDBT) was isolated and identified as Rhodococcus erythropolis USTB-03 by Institute of Microbiology, Chinese Academy of Sciences. Compared with glycerol and ethanol tested, glucose was found to be a promising sole carbon source for both the growth and the biodesulfurization activity of R, erythropolis USTB-03, and the maximum specific activity of 4,6-DMDBT biodesulfurization was 298.1 mmol 4,6-DMDBT/(kg ·h). It showed that the highest biodesulfurization activity of R. erythropolis USTB-03 was found at initial pH 7.0 in range from 4.0 to 9.0. R. erythropolis USTB-03 can selectively remove sulfur in the 4,6-DMDBT, and the dead-end product of 4, 6-DMDBT biodesulfurization was confirmed as 2-hydroxy- 3, 3'-dimethyl biphenyl (2-HDMBP), only the bond of C-S rather than C-C was cleaved, which is similar to the sulfur specific biodesuffufization pathway of dibenzothiophene.
出处 《科技导报》 CAS CSCD 2005年第11期10-13,共4页 Science & Technology Review
基金 国家自然科学基金(20377047)
关键词 红串红球菌USTB-03 4 6-二甲基二苯并噻吩 脱硫活性 脱硫途径 Rhodococcus Erythropolis USTB-03, 4,6-dimethyl dibenzothiophene, biodesulfurization activity, biodesulfurization pathway
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  • 1徐永强 等.石油学报:石油加工,2003,19(1):12-16.
  • 2Marroquin-Sanchez, G. & Ancheyta-Juarez, J Applied Catalysis A:Generel, 2001, 207(1):407-420.
  • 3Macaud M, Milenkovic A, Schulz E, et al. Journal of Catalysis,2000,193(1), 255-263.
  • 4Laudau M V. Catalysis Today , 1997,36(4):393-429.
  • 5Girgis, M J & Gates B C. Ind Eng Chem Res. 1991,30(9):2021 - 2058.
  • 6Gilman H. & Jcoby A L. J Org Chem, 1938, 3:108 - 119.
  • 7Kuchm-Caubere ,C Adach-Becker S, Fort Y, et al. Tetrahedron. 1996,52(27):9087-9092.
  • 8Bataille F, Lemberton J L, Michaud P, et. al Journal of Catalysis, 2000,191(1):409-422.
  • 9Larrubia M A, Gutierrez-Alejandre A, Ramirez J, Busca G. Applied Catalysis A: General, 2002,224(1): 167- 178.
  • 10徐永强.石油学报:石油加工,2000,19(1):12-16.

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