Hirasawa K, Ishii Y, Kobayashi M, Koizumi K, Maruhashi K
Bio-Refining Process Laboratory, Advanced Technology and Research Institute, Petroleum Energy Center, Shimizu-shi, Shizuoka, Japan.
Biosci Biotechnol Biochem. 2001 Feb;65(2):239-46. doi: 10.1271/bbb.65.239.
Rhodococcus erythropolis KA2-5-1 can desulfurize dibenzothiophene (DBT) into 2-hydroxybiphenyl. A cryptic plasmid, pRC4, which was derived from R. rhodochrous IFO3338, was combined with an Escherichia coli vector to construct an E. coli-Rhodococcus shuttle vector. The complete nucleotide sequence of 2582-bp pRC4 was analyzed. Based on the characteristics of its putative replication genes, pRC4 was assigned to the family of pAL5000-related replicons. The desulfurization gene cluster, dszABC, and the related reductase gene, dszD, cloned from KA2-5-1, were reintroduced into KA2-5-1 and efficiently expressed. The DBT desulfurization ability of the transformant carrying two dszABC clusters and one dszD on the vector was about 4-fold higher than that of the parent strain, and the transformant also showed improved desulfurization activity for light gas oil (LGO). Sulfur components in LGO before and after the reaction were analyzed with gas chromatography-atomic emission detection.
红平红球菌KA2-5-1可将二苯并噻吩(DBT)脱硫生成2-羟基联苯。一种源自红串红球菌IFO3338的隐蔽质粒pRC4与大肠杆菌载体结合,构建了一种大肠杆菌-红球菌穿梭载体。对2582 bp的pRC4的完整核苷酸序列进行了分析。基于其推定复制基因的特征,pRC4被归入与pAL5000相关的复制子家族。从KA2-5-1克隆的脱硫基因簇dszABC和相关还原酶基因dszD被重新导入KA2-5-1并高效表达。载体上携带两个dszABC簇和一个dszD的转化体的DBT脱硫能力比亲本菌株高约4倍,该转化体对轻质瓦斯油(LGO)的脱硫活性也有所提高。采用气相色谱-原子发射检测法分析了反应前后LGO中的硫成分。