Saxena I M, Lin F C, Brown R M
Department of Botany, University of Texas, Austin 78713-7640.
Plant Mol Biol. 1991 Jun;16(6):947-54. doi: 10.1007/BF00016067.
DNA sequencing of the region downstream of the cellulose synthase catalytic subunit gene of Acetobacter xylinum led to the identification of an open reading frame coding for a polypeptide of 86 kDa. The deduced amino acid sequence of this polypeptide matches from position 27 to 40 with the N-terminal amino acid sequence determined for a 93 kDa polypeptide that copurifies with the cellulose synthase catalytic subunit during purification of cellulose synthase. The cellulose synthase catalytic subunit gene and the gene encoding the 93 kDa polypeptide, along with other genes probably, are organized as an operon for cellulose biosynthesis in which the first gene is the catalytic subunit gene and the second gene codes for the 93 kDa polypeptide. The function of the 93 kDa polypeptide is not clear at present, however it appears to be tightly associated with the cellulose synthase catalytic subunit. Sequence analysis of the polypeptide shows that it is a membrane protein with a signal sequence at the N-terminal end and a transmembrane helix in the C-terminal region for anchoring it into the membrane.
木醋杆菌纤维素合酶催化亚基基因下游区域的DNA测序,导致鉴定出一个编码86 kDa多肽的开放阅读框。该多肽推导的氨基酸序列在第27至40位与在纤维素合酶纯化过程中与纤维素合酶催化亚基共纯化的93 kDa多肽所确定的N端氨基酸序列相匹配。纤维素合酶催化亚基基因和编码93 kDa多肽的基因,可能还有其他基因,被组织成一个用于纤维素生物合成的操纵子,其中第一个基因是催化亚基基因,第二个基因编码93 kDa多肽。目前93 kDa多肽的功能尚不清楚,然而它似乎与纤维素合酶催化亚基紧密相关。该多肽的序列分析表明,它是一种膜蛋白,在N端有一个信号序列,在C端区域有一个跨膜螺旋,用于将其锚定在膜中。