Stoner M T, Shively J M
Department of Biological Sciences, Clemson University, South Carolina 29634-1903.
FEMS Microbiol Lett. 1993 Mar 1;107(2-3):287-92. doi: 10.1111/j.1574-6968.1993.tb06044.x.
Both form I and II ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) genes were detected in Thiobacillus intermedius by heterologous hybridization using specific probes from Anacystis nidulans and Rhodobacter sphaeroides, respectively. However, only the previously reported form I enzyme could be demonstrated in cells grown under a number of different conditions. The reason(s) why the form II gene is not expressed in T. intermedius is/are not clear at this time. The form II gene was isolated from a lambda library by screening with the Rb. sphaeroides probe. A SalI fragment from this clone was ligated into pUC8 and transformed into Escherichia coli DH5 alpha. Subclones pTi20IIA and pTi20IIB representing both orientations relative to the lac promoter were isolated. Low levels of RuBisCO activity were detected in both induced and non-induced pTi20IIA indicating the probable expression from a T. intermedius promoter. Induced pTi20IIB produced much higher levels of enzyme activity. Analysis of cell-free extracts using sucrose density gradients confirmed the expression of a form II RuBisCO similar in size to that found in Rhodobacter capsulatus. Other Calvin cycle genes were not clustered with either the form I or form II genes.
分别使用来自集胞藻(Anacystis nidulans)和球形红杆菌(Rhodobacter sphaeroides)的特异性探针,通过异源杂交在中间硫杆菌(Thiobacillus intermedius)中检测到了I型和II型核酮糖-1,5-二磷酸羧化酶/加氧酶(RuBisCO)基因。然而,在多种不同条件下生长的细胞中,仅能证明存在先前报道的I型酶。目前尚不清楚II型基因在中间硫杆菌中不表达的原因。通过用球形红杆菌探针筛选λ文库,分离出了II型基因。将该克隆的一个SalI片段连接到pUC8中,并转化到大肠杆菌DH5α中。分离出相对于lac启动子呈两种方向的亚克隆pTi20IIA和pTi20IIB。在诱导和未诱导的pTi20IIA中均检测到低水平的RuBisCO活性,这表明可能是从中间硫杆菌启动子表达的。诱导的pTi20IIB产生了更高水平的酶活性。使用蔗糖密度梯度对无细胞提取物进行分析,证实了表达出一种大小与荚膜红杆菌(Rhodobacter capsulatus)中发现的II型RuBisCO相似的酶。其他卡尔文循环基因与I型或II型基因均未聚类。