TY - JOUR
T1 - Isolation and enzymological characterization of infected and uninfected cell protoplasts from root nodules of Glycine max
AU - Kouchi, Hiroshi
AU - Fukai, Katsuhiko
AU - Katagiri, Hiroki
AU - Minamisawa, Kiwamu
AU - Tajima, Shigeyuki
PY - 1988/7
Y1 - 1988/7
N2 - Infected and uninfected cell protoplasts were isolated from soybean (Glycine max L. Merr. cv. Akisengoku) root nodules and purified by the use of nylon mesh filters and discontinuous Percoll gradients. Activities of the enzymes involved in carbon and nitrogen metabolism were measured in cytoplasmic fractions of purified protoplasts, as well as in the bacteroids isolated from infected cell protoplasts and in the cortical tissues after enzymatic digestion of the central zone of the nodules. A high degree of purity of both infected and uninfected cells was demonstrated by microscopic observations and assays of β‐hydroxybutyrate dehydrogenase (EC 1.1.1.30) and uricase (EC 1.7.3.3) activities and leghemoglobin contents. As a whole, higher specific activities of enzymes of glycolysis were found in the cortical and uninfected cells than in the infected cells. The activities of glycolytic enzymes were extremely low in the bacteroids. Invertase (EC 3.2.1.26) was highly localized in the cortex. However, activity of sucrose synthase (EC 2.4.1.13) was highest in the cytosol of infected cells. Alcohol dehydrogenase (EC 1.1.1.1) and lactate dehydrogenase (EC 1.1.1.27) activities were much higher in uninfected than in infected cells. Specific activities of enzymes for nitrogen assimilation, that is, glutamine synthetase (EC 6.3.1.2), glutamate synthase (EC 1.4.1.14), aspartate (EC 2.6.1.1) and alanine (EC 2.6.1.2) aminotransferase were several‐fold higher in uninfected cells than in the infected cells. The results are discussed in relation to the possible cellular organization of carbon and nitrogen metabolism in soybean root nodules.
AB - Infected and uninfected cell protoplasts were isolated from soybean (Glycine max L. Merr. cv. Akisengoku) root nodules and purified by the use of nylon mesh filters and discontinuous Percoll gradients. Activities of the enzymes involved in carbon and nitrogen metabolism were measured in cytoplasmic fractions of purified protoplasts, as well as in the bacteroids isolated from infected cell protoplasts and in the cortical tissues after enzymatic digestion of the central zone of the nodules. A high degree of purity of both infected and uninfected cells was demonstrated by microscopic observations and assays of β‐hydroxybutyrate dehydrogenase (EC 1.1.1.30) and uricase (EC 1.7.3.3) activities and leghemoglobin contents. As a whole, higher specific activities of enzymes of glycolysis were found in the cortical and uninfected cells than in the infected cells. The activities of glycolytic enzymes were extremely low in the bacteroids. Invertase (EC 3.2.1.26) was highly localized in the cortex. However, activity of sucrose synthase (EC 2.4.1.13) was highest in the cytosol of infected cells. Alcohol dehydrogenase (EC 1.1.1.1) and lactate dehydrogenase (EC 1.1.1.27) activities were much higher in uninfected than in infected cells. Specific activities of enzymes for nitrogen assimilation, that is, glutamine synthetase (EC 6.3.1.2), glutamate synthase (EC 1.4.1.14), aspartate (EC 2.6.1.1) and alanine (EC 2.6.1.2) aminotransferase were several‐fold higher in uninfected cells than in the infected cells. The results are discussed in relation to the possible cellular organization of carbon and nitrogen metabolism in soybean root nodules.
KW - Glycine max
KW - alanine aminetransferase
KW - alcohol dehydrogenase
KW - aspartate aminotransferase
KW - carbon metabolism
KW - enzyme compartmentation
KW - glutamate synthase
KW - glutamine synthetase
KW - invertase
KW - lactate dehydrogenase
KW - root nodules
KW - soybean
KW - sucrose synthase
KW - uricase
KW - β‐hydroxybutyrate dehydrogenase
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U2 - 10.1111/j.1399-3054.1988.tb00606.x
DO - 10.1111/j.1399-3054.1988.tb00606.x
M3 - Article
AN - SCOPUS:0000684138
SN - 0031-9317
VL - 73
SP - 327
EP - 334
JO - Physiologia Plantarum
JF - Physiologia Plantarum
IS - 3
ER -