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. 2022 Jan 3;15(5):1586–1597. doi: 10.1111/1751-7915.13999

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© 2021 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd.

This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

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Fig. 3 — Production of P(3HB‐co‐4HB) by OM‐defected H. bluephagenesis strains cultivated in 500‐ml shake flasks without IPTG induction.

A. H. bluephagenesis TDH4ΔphaP1 has a constitutive P_porin promotor for phaCAB expression.

B. Shake flask procedure of P(3HB‐co‐4HB) production: 5 g l⁻¹ of γ‐butyrolactone was added at OD₆₀₀ = 6 (≈ 8 h).

C–D. Growth and P(3HB‐co‐4HB) production in MM50 containing IPTG and γ‐butyrolactone. Data are expressed as the mean ± SD from biologically independent triplicate experiments.