Genetic manipulation of nitrogenase and key glutamate-forming enzymes can provide mutants that excrete fixed N2 as NH4+. A derepressed N2 fixation mutant (SK-24) has been isolated, which excretes up to 20.2 micro mol of fixed N2 as NH4+ per mg of cell protein in 24 hr at room temperature. Biochemical analysis shows that this mutant, which requires glutamate for growth, releases fixed N2 as NH4+ into the environment because of (i) constitutive synthesis of nitrogenase and (ii) genetic blocks resulting in losses of glutamate synthase L-glutamine:2-oxoglutarate aminotransferase (NADPH oxidizing), EC 2.6.1.53 and glutamate dehydrogenase L-glutamate:NADP oxidoreductase (deaminating), EC 1.4.1.4 activities, enzymes essential for NH4+ assimilation into cell material. The parent strain (asm-1), missing only glutamate synthase activity, also actively excretes NH4+ during early phases of its growth but eventually reutilizes the NH4+. A maximum yield of 4.0 micro mol of NH4+/ml per 24 hr has been noted for asm-1 only during the growth period. Biosynthesis of NH4+ proceeds at the expense of a variety of fermentable sugars, such as sucrose or glucose, with a maximum energy conversion efficiency of about 5 glucose degraded per NH4+ formed. The use of microbes for production of NH4+ fertilizer is discussed.
Description
Microbial Production of Ammonium Ion from Nitrogen -- Shanmugam and Valentine 72 (1): 136 -- Proceedings of the National Academy of Sciences
%0 Journal Article
%1 K.T._Shanmugam01151975
%A Shanmugam, K. T.
%A Valentine, R. C.
%D 1975
%J Proceedings of the National Academy of Sciences
%K NH4 ammonia fermentation fertilizer glucose glutemate microbial mutant nitrogenase sucrose
%N 1
%P 136-139
%R 10.1073/pnas.72.1.136
%T Microbial Production of Ammonium Ion from Nitrogen
%U http://www.pnas.org/cgi/content/abstract/72/1/136
%V 72
%X Genetic manipulation of nitrogenase and key glutamate-forming enzymes can provide mutants that excrete fixed N2 as NH4+. A derepressed N2 fixation mutant (SK-24) has been isolated, which excretes up to 20.2 micro mol of fixed N2 as NH4+ per mg of cell protein in 24 hr at room temperature. Biochemical analysis shows that this mutant, which requires glutamate for growth, releases fixed N2 as NH4+ into the environment because of (i) constitutive synthesis of nitrogenase and (ii) genetic blocks resulting in losses of glutamate synthase L-glutamine:2-oxoglutarate aminotransferase (NADPH oxidizing), EC 2.6.1.53 and glutamate dehydrogenase L-glutamate:NADP oxidoreductase (deaminating), EC 1.4.1.4 activities, enzymes essential for NH4+ assimilation into cell material. The parent strain (asm-1), missing only glutamate synthase activity, also actively excretes NH4+ during early phases of its growth but eventually reutilizes the NH4+. A maximum yield of 4.0 micro mol of NH4+/ml per 24 hr has been noted for asm-1 only during the growth period. Biosynthesis of NH4+ proceeds at the expense of a variety of fermentable sugars, such as sucrose or glucose, with a maximum energy conversion efficiency of about 5 glucose degraded per NH4+ formed. The use of microbes for production of NH4+ fertilizer is discussed.
@article{K.T._Shanmugam01151975,
abstract = {Genetic manipulation of nitrogenase and key glutamate-forming enzymes can provide mutants that excrete fixed N2 as NH4{}+. A derepressed N2 fixation mutant (SK-24) has been isolated, which excretes up to 20.2 {micro} mol of fixed N2 as NH4{}+ per mg of cell protein in 24 hr at room temperature. Biochemical analysis shows that this mutant, which requires glutamate for growth, releases fixed N2 as NH4{}+ into the environment because of (i) constitutive synthesis of nitrogenase and (ii) genetic blocks resulting in losses of glutamate synthase [L-glutamine:2-oxoglutarate aminotransferase (NADPH oxidizing), EC 2.6.1.53] and glutamate dehydrogenase [L-glutamate:NADP oxidoreductase (deaminating), EC 1.4.1.4] activities, enzymes essential for NH4{}+ assimilation into cell material. The parent strain (asm-1), missing only glutamate synthase activity, also actively excretes NH4{}+ during early phases of its growth but eventually reutilizes the NH4{}+. A maximum yield of 4.0 {micro} mol of NH4{}+/ml per 24 hr has been noted for asm-1 only during the growth period. Biosynthesis of NH4{}+ proceeds at the expense of a variety of fermentable sugars, such as sucrose or glucose, with a maximum energy conversion efficiency of about 5 glucose degraded per NH4{}+ formed. The use of microbes for production of NH4{}+ fertilizer is discussed.
},
added-at = {2008-05-17T04:57:01.000+0200},
author = {Shanmugam, K. T. and Valentine, R. C.},
biburl = {https://www.bibsonomy.org/bibtex/295c6c1497f90b2ac05af5717c6764dd0/thulefoth},
description = {Microbial Production of Ammonium Ion from Nitrogen -- Shanmugam and Valentine 72 (1): 136 -- Proceedings of the National Academy of Sciences},
doi = {10.1073/pnas.72.1.136},
eprint = {http://www.pnas.org/cgi/reprint/72/1/136.pdf},
interhash = {4a03fba56fa5f9528c262871ce92fd5f},
intrahash = {95c6c1497f90b2ac05af5717c6764dd0},
journal = {Proceedings of the National Academy of Sciences},
keywords = {NH4 ammonia fermentation fertilizer glucose glutemate microbial mutant nitrogenase sucrose},
number = 1,
pages = {136-139},
timestamp = {2008-05-17T04:57:02.000+0200},
title = {{Microbial Production of Ammonium Ion from Nitrogen}},
url = {http://www.pnas.org/cgi/content/abstract/72/1/136},
volume = 72,
year = 1975
}