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. 2012 May 18;63(12):4403–4417. doi: 10.1093/jxb/ers115

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© 2012 The Author(s).

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)

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Fig. 9. — Carotenoid analysis and cellular inspection of co-transformed lines (35S::CrtB/DSM2) and M-33 (35S::CrtB). Via., violaxanthin; Zea., zeaxanthin; Lut., lutein; Phy., phytoene; α-Car., α-carotene; β-Car., β-carotene. Values and bars represent the means and ±SD (n=3 replicate experiments), respectively. ** Indicates that the values are significantly different compared with M-33 at the significance level of P <0.01. (A) Normal light microscopy. (B) Polarization microscopy (arrows show the dot-crystals attaching to the amyloplasts). (C) Ultrastructure of amyloplast (arrow shows the electron-transparent plastoglobules; S, starch granule). The bar in picture (A) represents 10 μm.