Nucleotide sequence of Arabidopsis thaliana arginase expressed in yeast.
نویسندگان
چکیده
Arginase (L-Arg amidinohydrolase, EC 3.5.3.1) catalyzes the hydrolysis of L-Arg to urea and L-Orn. Orn is a precursor of Pro and polyamines and urea N is recycled by urease-catalyzed hydrolysis to ammonia (Polacco and Holland, 1993). Many plant species store much seed protein N in Arg (VanEtten et al., 1963), significant quantities of which are released and catabolized during germination (Polacco and Holland, 1993). In soybean axes arginase activity increases sharply during germination (Kang and Cho, 1990), consistent with considerable urea accumulation in urease-negative soybean seedlings (Stebbins et al., 1991). The Arubidopsis 12s globulin (Pang et al., 1988) and 2s albumin (Krebbers et al., 1988) seed storage proteins have a deduced Arg content of 7.0 and 6.9 mo1 %, respectively, whereas the Arg content of an “average” protein is 3.0 mo1 % (VanEtten et al., 1963). Conversion of Arubidopsis seed storage protein to seedling protein potentially involves Arg breakdown, consistent with a 10-fold increase in seedling arginase activity during the Oto 6-d after germination interval (Zonia et al., 1995). We report the nucleotide sequence of an Arubidopsis arginase cDNA recovered by its complementation of a yeast (Succkuromyces cerevisiue) arginase-deficient (curl) mutant (Table I). The pertinent genotype of the yeast host was curl,durl,ura3-52, a nonreverting uracil auxotroph (uru3-52) unable to utilize either Arg (curl) or urea (dur l ) as sole N source. URA+ transformants (recovered via the method of Gietz et al., 1992) harboring members of a two-leaf-stage Arubidopsis cDNA library (in yeast-Esckerickiu cozi shuttle vector pFL61; Minet et al., 1992) were replica plated to medium with Arg as sole N source. One URA’ isolate grew consistently on this medium and its plasmid transmitted this trait to new host cells. We concluded that this isolate expressed an arginase because it accumulated urea in the presence of Arg and because its cDNA insert showed size and sequence sim-
منابع مشابه
Yeast Two Hybrid cDNA Screening of Arabidopsis thaliana for SETH4 Protein Interaction
SETH4 coding sequence with 2013 bp is a member of gene family expressed in gametophytic tissues of Arabidopsis thaliana. This fragment was PCR amplified using Kod Hi Fi DNA polymerase enzyme. This fragment was cloned into pGBKT7 bate vector and transformed E. coli DH5? cells containing vector were selected on LB medium containing Kanamycin. Finally, pGBKT7-SETH4 bate was transformed into yeast ...
متن کاملIdentification and Expression Analysis of Two Arabidopsis LRR-Protein Encoding Genes Responsive to Some Abiotic Stresses
AbstractTwo Arabidopsis thaliana genes, psr9.2 and psr9.4 appearedto be highly similar to a phosphate-starved induced gene,psr9, isolated from Brassica nigra suspension cells.Sequence analysis classified the encoded polypeptides asmembers of leucine-rich repeat (LRR) proteins superfamily.The sequence of psr9 proteins comprise a unique N-terminalregion e...
متن کاملThe impacts of TRR14 over-expression on Arabidopsis thaliana growth and some photosynthetic parameters
Background: TRR14 protein is a small member of a multi-gene family in Arabidopsis and is the first ones found during screening of seedlings for their resistant to the trehalose sugar.Objectives: Characterization ofTRR14 over-expressed plants with respect to morphological changes, growth and photosynthesis related parameters.Materials and methods: TRR14gene was isolated from Arabidop...
متن کاملCloning, yeast expression, and characterization of the coupling of two distantly related Arabidopsis thaliana NADPH-cytochrome P450 reductases with P450 CYP73A5.
Two NADPH-cytochrome P450 reductase-encoding cDNAs were isolated from an Arabidopsis cDNA library by metabolic interference in a Saccharomyces cerevisiae mutant disrupted for its endogenous cpr1 gene. ATR1 encodes a protein of 692 amino acids, while ATR2 encodes either a 712-residue protein (ATR2-1), or a 702-residue protein (ATR2-2) depending on the choice of the initiation codon. Comparative ...
متن کاملCloning and expression in yeast of a higher plant chorismate mutase. Molecular cloning, sequencing of the cDNA and characterization of the Arabidopsis thaliana enzyme expressed in yeast.
Chorismate mutase (EC 5.4.99.5) catalyzes the first step in the branch of the shikimate pathway which leads to the aromatic amino acids, phenylalanine and tyrosine. We have isolated a cDNA for this enzyme from the higher plant, Arabidopsis thaliana, by complementing a yeast strain (aro7) with a cDNA library from A. thaliana. This is the first chorismate mutase cDNA isolated from a plant. It enc...
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:
- Plant physiology
دوره 107 4 شماره
صفحات -
تاریخ انتشار 1995