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A calcium‐binding protein with similarity to serum albumin localized to the ER‐Golgi network and cell walls of spinach ( Spinacia oleracea )
Author(s) -
Lait Cameron G.,
Zwiazek Janusz J.
Publication year - 2001
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1034/j.1399-3054.2001.1120402.x
Subject(s) - spinacia , biochemistry , spinach , isoelectric point , biology , endoplasmic reticulum , cell wall , chemistry , chromatography , chloroplast , enzyme , gene
Using polyclonal antibodies raised against human serum albumin (HSA), a 70‐kDa microsomal protein with an isoelectric point of approximately 6.5 was detected in spinach ( Spinacia oleracea L.). The protein was purified by selective ammonium sulfate precipitation and anion exchange HPLC. The protein shared 100% identity with the first 15 amino acids at the NH 2 terminus of HSA, including the X‐X‐H amino acid region, which was identified in HSA as being responsible for binding of copper, zinc, indole derivatives and calcium. Blue staining of the protein with the cationic carbocyanine dye ‘Stains‐all’ and 45 Ca overlay following SDS‐PAGE also suggest that the 70‐kDa plant protein binds calcium. The protein reacted positively with carbohydrate specific thymol stain, and the carbohydrates associated with the protein were identified by gas chromatography‐mass spectrometry (GC‐MS) as galactose and galacturonic acid. The 70‐kDa plant protein was present in the detergent‐poor phase following Triton X‐114 extraction of the microsomal proteins. Cell fractionation using continuous sucrose gradients showed that the protein is present in membrane fractions with high activity of endoplasmic reticulum (ER) and Golgi marker enzymes. Using nitrocellulose tissue prints probed with anti‐HSA antibodies, we demonstrated that the protein is present in the apoplastic space of petioles, suggesting that the protein is secreted to the apoplast of cortex cells in plants. Localization and binding properties suggest that the plant protein identified in the present study may participate in secretion processes, possibly involved with the transport of precursors required for cell‐wall synthesis.