Richardson D J, McEwan A G, Page M D, Jackson J B, Ferguson S J
School of Biochemistry, University of Birmingham, England.
Eur J Biochem. 1990 Nov 26;194(1):263-70. doi: 10.1111/j.1432-1033.1990.tb19452.x.
The involvement of cytochromes in the electron-transport pathway to the periplasmic NO3- reductase of Rhodobacter capsulatus was studied in cells grown photoheterotrophically in the presence of nitrate with butyrate as carbon source. The specific rate of NO3- reduction by such cells was five times higher than when malate was carbon source. Reduced minus NO3(-)-oxidized spectra of cells had peaks in the alpha-band region for cytochromes at 552 nm and 559 nm, indicating the involvement of c- and b-type cytochromes in the electron-transport pathway to NO3-. The total ferricyanide-oxidizable cytochrome that was also oxidized in the steady state by NO3- was greater in cells grown with butyrate rather than malate. Low concentrations of cyanide inhibited NO3- reduction. Neither CN-, nor a previously characterized inhibitor of NO3- reduction, 2-n-heptyl-4-hydroxyquinoline N-oxide, prevented the oxidation of the cytochromes by NO3-. This suggested a site of action for these inhibitors on the reducing side of the b- and c-type cytochromes involved in electron transport to the NO3- reductase. The predominant cytochrome in a periplasmic fraction prepared from cells of R. capsulatus grown on butyrate medium was cytochrome c2 but a c-type cytochrome with an alpha-band reduced absorbance maximum at 552 nm could also be identified. The reduced form of this latter cytochrome, but not that of cytochrome c2, was oxidized upon addition of NO3- to a periplasmic fraction. The NO3(-)-oxidizable cytochrome co-purified with the periplasmic NO3- reductase through fractionation procedures that included ammonium sulphate precipitation, gel filtration at low and high salt concentrations, and ion-exchange chromatography. A NO3(-)-reductase-cytochrome-c552 redox complex that comprised two types of polypeptide, a nitrate reductase subunit and a c-type cytochrome subunit, was purified. The polypeptides were separated when the complex was chromatographed on a phenyl-Sepharose hydrophobic chromatography column.
在以丁酸盐作为碳源、硝酸盐存在的条件下光异养生长的荚膜红细菌细胞中,研究了细胞色素参与电子传递途径至周质硝酸还原酶的情况。这类细胞还原硝酸盐的比速率比以苹果酸盐作为碳源时高五倍。细胞的还原态减去硝酸盐氧化态光谱在细胞色素的α波段区域于552纳米和559纳米处有峰值,表明c型和b型细胞色素参与了向硝酸盐的电子传递途径。在以丁酸盐而非苹果酸盐生长的细胞中,总铁氰化物可氧化的细胞色素(在稳态下也被硝酸盐氧化)更多。低浓度的氰化物抑制硝酸盐还原。无论是氰离子,还是先前表征的硝酸盐还原抑制剂2-正庚基-4-羟基喹啉N-氧化物,都不能阻止细胞色素被硝酸盐氧化。这表明这些抑制剂在参与向硝酸盐还原酶电子传递的b型和c型细胞色素的还原侧有作用位点。从在丁酸盐培养基上生长的荚膜红细菌细胞制备的周质组分中,主要的细胞色素是细胞色素c2,但也能鉴定出一种α波段还原吸光度最大值在552纳米的c型细胞色素。向周质组分中添加硝酸盐后,后一种细胞色素的还原形式而非细胞色素c2的还原形式被氧化。可被硝酸盐氧化的细胞色素通过包括硫酸铵沉淀、低盐和高盐浓度下的凝胶过滤以及离子交换色谱在内的分级分离程序与周质硝酸还原酶共纯化。纯化得到了一种由两种类型多肽组成的硝酸盐还原酶 - 细胞色素 - c552氧化还原复合物,一种是硝酸盐还原酶亚基,另一种是c型细胞色素亚基。当复合物在苯基 - 琼脂糖疏水色谱柱上进行色谱分离时,多肽被分离。