The reaction takes place in the opposite direction. Part of a bacterial polyamine biosynthesis pathway. L-aspartate 4-semialdehyde and propane-1,3-diamine/putrescine form a Schiff base that is reduced to form carboxynorspermidine/carboxyspermidine, respectively . The enzyme from the bacterium Vibrio cholerae is essential for biofilm formation . The enzyme from Campylobacter jejuni only produces carboxyspermidine in vivo even though it also can produce carboxynorspermidine in vitro .
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SYSTEMATIC NAME
IUBMB Comments
carboxynorspermidine:NADP+ oxidoreductase
The reaction takes place in the opposite direction. Part of a bacterial polyamine biosynthesis pathway. L-aspartate 4-semialdehyde and propane-1,3-diamine/putrescine form a Schiff base that is reduced to form carboxynorspermidine/carboxyspermidine, respectively [1]. The enzyme from the bacterium Vibrio cholerae is essential for biofilm formation [2]. The enzyme from Campylobacter jejuni only produces carboxyspermidine in vivo even though it also can produce carboxynorspermidine in vitro [3].
about 14fold increase of activity at 20 mM. Without addition of dithiothreitol to the assay mixture, only 7% of the maximum activity is detected in the purified enzyme
accumulation of the precursor putrescine in the CASDH mutant The mutant accumulates homospermidine, which requires a homospermidine synthase (hss) homologue. Agrobacterium tumefaciens mutants with diminished levels of the polyamine spermidine are stimulated for biofilm formation, and exogenous provision of spermidine decreases biofilm formation. Spermidine is also essential for Agrobacterium tumefaciens growth, but the related polyamine norspermidine exogenously rescues growth and does not diminish biofilm formation, the growth requirement and biofilm control are separable. Exogenous spermidine and norspermidine restore prototrophic growth for CASDH and CASDC mutants, but only spermidine inhibits biofilm formation. CASDH and CASDC mutants accumulate homospermidine via a homospermidine synthase homologue
the DELTACASDH (Atu4170) mutant strain accumulates putrescine and homospermidine but lacks spermidine. The DELTA4170 strain contains endogenously produced putrescine and homospermidine, but there is no growth of this strain in the absence of exogenously supplied polyamines. Homospermidine biosynthesis is induced only after spermidine depletion. The DELTACASDH strain grows well in medium with added exogenous N8-acetylspermidine
the DELTACASDH (Atu4170) mutant strain accumulates putrescine and homospermidine but lacks spermidine. The DELTA4170 strain contains endogenously produced putrescine and homospermidine, but there is no growth of this strain in the absence of exogenously supplied polyamines. Homospermidine biosynthesis is induced only after spermidine depletion. The DELTACASDH strain grows well in medium with added exogenous N8-acetylspermidine
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malfunction
Vibrio cholerae serotype O1 El Tor
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deletion of the enzyme leads to a 50-60% reduction in growth rate of planktonic cells and severely reduced biofilm formation
in an alternative pathway (alternate to the pathway via S-adenosyl-L-methionine), putrescine is first converted into carboxyspermidine with the precursor L-aspartate beta-semialdehyde by the enzyme carboxyspermidine dehydrogenase (CASDH), and then carboxyspermidine is converted to spermidine by carboxyspermidine decarboxylase (CASDC). Spermidine is an essential metabolite in Agrobacterium tumefaciens and is synthesized from putrescine via the stepwise actions of carboxyspermidine dehydrogenase (CASDH) and carboxyspermidine decarboxylase (CASDC)
when spermidine levels are pharmacologically decreased, synthesis of spermine from spermidine is induced via the same biosynthetic enzymes, carboxyspermidine dehydrogenase and carboxyspermidine decarboxylase that produce spermidine from putrescine. Spermidine represses spermine biosynthesis, but when spermidine levels decrease, it is then converted by carboxyspermidine dehydrogenase and decarboxylase enzymes to spermine, which is resistant to retroconversion and constitutes a sequestered pool of protected 1,3-diaminopropane modules required for growth. Polyamine biosynthesis in Agrobacterium tumefaciens strain C58, overview
when spermidine levels are pharmacologically decreased, synthesis of spermine from spermidine is induced via the same biosynthetic enzymes, carboxyspermidine dehydrogenase and carboxyspermidine decarboxylase that produce spermidine from putrescine. Spermidine represses spermine biosynthesis, but when spermidine levels decrease, it is then converted by carboxyspermidine dehydrogenase and decarboxylase enzymes to spermine, which is resistant to retroconversion and constitutes a sequestered pool of protected 1,3-diaminopropane modules required for growth. Polyamine biosynthesis in Agrobacterium tumefaciens strain C58, overview
spermidine is an essential metabolite in Agrobacterium tumefaciens and is synthesized from putrescine via the stepwise actions of carboxyspermidine dehydrogenase (CASDH) and carboxyspermidine decarboxylase (CASDC). Spermidine is essential for Agrobacterium tumefaciens growth, growth requirement and biofilm control are separable. Polyamine control of biofilm formation appears to function via effects on the cellular second messenger cyclic diguanylate monophosphate, regulating the transition from a freeliving to a surface-attached lifestyle
when spermidine levels are pharmacologically decreased, synthesis of spermine from spermidine is induced via the same biosynthetic enzymes, carboxyspermidine dehydrogenase and carboxyspermidine decarboxylase that produce spermidine from putrescine. Essential role of a terminal 1,3-diaminopropane moiety in growth of Agrobacterium tumefaciens
when spermidine levels are pharmacologically decreased, synthesis of spermine from spermidine is induced via the same biosynthetic enzymes, carboxyspermidine dehydrogenase and carboxyspermidine decarboxylase that produce spermidine from putrescine. Essential role of a terminal 1,3-diaminopropane moiety in growth of Agrobacterium tumefaciens
transposon mutagenesis of Agrobacterium tumefaciens strain C58 to knockdown enzyme CASDH performed with the mariner minitransposon Himar1, phenotype, overview. In-frame CASDH and CASDC gene deletion mutants have severe growth defects in minimal medium but are rescued in this respect by exogenous addition of exogenous polyamines that supply the 1,3-diaminopropane group, including spermidine. The severe growth defect of the CASDH and CASDC mutants also manifested itself as a severe biofilm deficiency
transposon mutagenesis of Agrobacterium tumefaciens strain C58 to knockdown enzyme CASDH performed with the mariner minitransposon Himar1, phenotype, overview. In-frame CASDH and CASDC gene deletion mutants have severe growth defects in minimal medium but are rescued in this respect by exogenous addition of exogenous polyamines that supply the 1,3-diaminopropane group, including spermidine. The severe growth defect of the CASDH and CASDC mutants also manifested itself as a severe biofilm deficiency
Purification and some properties of carboxynorspermidine synthase participating in a novel biosynthetic pathway for norspermidine inVibrio alginolyticus