Affiliation:
1. Department of Fermentation Technology, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8527, Japan
Abstract
ABSTRACT
Klebsiella aerogenes
ATCC 9621 was able to utilize phosphonates (P
n
), including aminoethylphosphonate, ethylphosphonate, methylphosphonate (MP
n
), and phosphonoacetate, and inorganic phosphite (P
t
) as sole sources of phosphorus (P). The products of the
phn
gene cluster were absolutely required for P
n
breakdown and P
t
oxidation to inorganic phosphate (P
i
) in this organism. To determine if
K. aerogenes
ATCC 9621 could be engineered to enhance the utilization of P
n
and P
t
, a multicopy plasmid, pBI05, which carried the entire
phn
gene cluster, was introduced into this strain. Despite the increased dosage of the
phn
genes,
K. aerogenes
ATCC 9621(pBI05) could utilize only up to 1.1-fold more P
n
and P
t
than did the control strain with the parent vector alone. These results suggested that P
i
, which was generated from P
n
and P
t
, might limit further utilization of these P compounds. Consequently, to convert the resulting P
i
to polyphosphate (polyP), the plasmid pKP28, which carried the
K. aerogenes ppk
gene (which encodes polyP kinase), was introduced into
K. aerogenes
ATCC 9621(pBI05). Overexpression of the
ppk
gene in
K. aerogenes
ATCC 9621(pBI05, pKP28) resulted in a 2.5-fold increase in P
t
utilization over that of the control strain. This recombinant strain also accumulated approximately sixfold more P than did the control strain when the cells were grown with MP
n
as a sole source of P.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
29 articles.
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