Laboratory for Nitrogen Fixation Research, Oregon State University, Corvallis, Oregon 97331.
Proc Natl Acad Sci U S A. 1983 Apr;80(8):2253-7. doi: 10.1073/pnas.80.8.2253.
Soybean plants and Rhizobium japonicum 122 DES, a hydrogen uptake-positive strain, were cultured in media purified to remove Ni. Supplemental Ni had no significant effect on the dry matter or total N content of plants. However, the addition of Ni to both nitrate-grown and symbiotically grown plants resulted in a 7- to 10-fold increase in urease activity (urea amidohydrolase, EC 3.5.1.5) in leaves and significantly increased the hydrogenase activity (EC 1.18.3.1) in isolated nodule bacteroids. When cultured under chemolithotrophic conditions, free-living R. japonicum required Ni for growth and for the expression of hydrogenase activity. Hydrogenase activity was minimal or not detectable in cells incubated either without Ni or with Ni and chloramphenicol. Ni is required for derepression of hydrogenase activity and apparently protein synthesis is necessary for the participation of Ni in hydrogenase expression. The addition of Cr, V, Sn, and Pb in place of Ni failed to stimulate the activity of hydrogenase in R. japonicum and urease in soybean leaves. The evidence indicates that Ni is an important micronutrient element in the biology of the soybean plant and R. japonicum.
大豆植株和根瘤菌 122DES(一种吸氢阳性菌株)在去除镍的培养基中培养。补充镍对植物的干物质或总氮含量没有显著影响。然而,将镍添加到硝酸盐生长和共生生长的植物中,导致叶片中的脲酶活性(尿素酰胺水解酶,EC 3.5.1.5)增加了 7-10 倍,并且显著增加了分离的根瘤菌细菌的氢化酶活性(EC 1.18.3.1)。当在化能自养条件下培养时,自由生活的根瘤菌需要镍来生长和表达氢化酶活性。在没有镍或有镍和氯霉素的情况下孵育的细胞中,氢化酶活性最小或无法检测到。镍对于氢化酶活性的去阻遏是必需的,显然蛋白质合成对于镍参与氢化酶表达是必需的。用 Cr、V、Sn 和 Pb 代替镍,未能刺激根瘤菌中的氢化酶活性和大豆叶片中的脲酶活性。这一证据表明,镍是大豆植株和根瘤菌生物学中的一种重要微量元素。