The Mechanism of 2-keto-3-deoxy-6-phosphogluconic Aldolase.
نویسندگان
چکیده
In the original study of 2-keto-3-deoxy-6-phosphogluconic aldolase (I), and in subsequent experiments, the net synthesis of 2-keto-3-deoxy-6-phosphogluconate from the cleavage products could not be demonstrated. The present experiments were undertaken to clarify this point and to test the conformity of the reaction catalyzed by 2-keto-3-deoxy-6-phosphogluconic aldolase to the general characteristics of aldolase reactions. The data reported herein establish the reversibility of the reaction and show the tritium exchange behavior to be consistent with known aldolase reactions.
منابع مشابه
The Substrate Analog, Bromopyruvate, as a Bridging Agent for the Active Site of Z-Keto-3-deoxy-6-phosphogluconic Aldolase CHEMICAL EVIDEKCE FOR A CARBOXYLATE ADJACEPU’T TO THE SCHIFF’S BASE-FORMING LYSINE*
The enzyme, 2-keto-3-deoxy-6-phosphogluconic aldolase is inactivated by the substrate analog, bromopyruvate. Inactivation results from either an active site carboxyl group or a cysteine being alkylated by bromopyruvate. Treatment of enzyme inactivated by carboxylate ester formation with borohydride produces the secondary amine resulting from reduction of a Schiff’s base between the covalently f...
متن کاملRedesigning Aldolase Stereoselectivity by Homologous Grafting
The 2-deoxy-d-ribose-5-phosphate aldolase (DERA) offers access to highly desirable building blocks for organic synthesis by catalyzing a stereoselective C-C bond formation between acetaldehyde and certain electrophilic aldehydes. DERA´s potential is particularly highlighted by the ability to catalyze sequential, highly enantioselective aldol reactions. However, its synthetic use is limited by t...
متن کاملAnalysis of cloned structural and regulatory genes for carbohydrate utilization in Pseudomonas aeruginosa PAO.
Five of the genes required for phosphorylative catabolism of glucose in Pseudomonas aeruginosa were ordered on two different chromosomal fragments. Analysis of a previously isolated 6.0-kb EcoRI fragment containing three structural genes showed that the genes were present on a 4.6-kb fragment in the order glucose-binding protein (gltB)-glucokinase (glk)-6-phosphogluconate dehydratase (edd). Two...
متن کاملSugar metabolism in the extremely halophilic bacterium Salinibacter ruber.
Growth of Salinibacter ruber, a red, extremely halophilic bacterium phylogenetically affiliated with the Flavobacterium/Cytophaga branch of the domain Bacteria, is stimulated by a small number of sugars (glucose, maltose, starch at 1 g l(-1)). Glucose consumption starts after other substrates have been depleted. Glucose metabolism proceeds via a constitutive, salt-inhibited hexokinase and a con...
متن کاملLocations of the zwf, edd, and eda genes on the Escherichia coli physical map.
The 40.5-min region of the Escherichia coli map contains the zwf gene, which encodes glucose-6-phosphate dehydrogenase, an enzyme of the pentose phosphate pathway, and the edd and eda genes, which encode 6-phosphogluconate dehydratase and 2-keto-3-deoxy-6-phosphogluconate aldolase, respectively, the key enzymes of the Entner-Doudoroff pathway (4). These three genes are tightly linked, and their...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of biological chemistry
دوره 239 شماره
صفحات -
تاریخ انتشار 1964