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Effect of salting process on the histological structure of salmon flesh

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HAL Id: hal-01595471

https://hal.archives-ouvertes.fr/hal-01595471

Submitted on 26 Sep 2017

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Effect of salting process on the histological structure of salmon flesh

Olivier Loison, Weijunlang Jiang, Annie Venien, Oulyana Gaubain, Chantal Cazevieille, Thierry Astruc

To cite this version:

Olivier Loison, Weijunlang Jiang, Annie Venien, Oulyana Gaubain, Chantal Cazevieille, et al.. Effect of salting process on the histological structure of salmon flesh. International Symposium on Food Nutrition and Health, May 2017, Dalian, China. 2017. �hal-01595471�

(2)

International Symposium On Food Nutrition and Health

Dalian, May 26-28, 2017

Results

Effect of salting process on the

histological structure of salmon flesh

Olivier Loison1, Weijunlang Jiang1, Annie Vénien1, Ouliana Gaubain1, Chantal Cazevieille2, Thierry Astruc1

Context and objectives Conclusions

Atlantic Salmon, Salmo Salar, is composed of approximately 70%

water, 19% protein, 10% lipid and 1% small nutrients.

Smoked salmon comes from the processing of fresh salmon: the fillets are removed from the fish, salted and then smoked. Salting can be carried out with dry salt or by brine injection.

û Effect of salting:

- Dry Salt: causes solubilisation of sarcomeres at Z-lines.

- Brine Injection: causes the swelling of myofibrils.

The increase in water holding capacity of myofibrillar proteins, is reflected by the swelling of myofibrils.

û Effect of Smoking: not significant change after salting.

Our goal was to characterize the muscle structure of smoked salmon according to the

salting process.

Material and Methods

10 µm cryosections

70 nm sections

Image analysis (Image J)

Staining Cryofixation:

Isopentane cooled by liquid nitrogen

Muscle samples (1x1x1,5 cm)

Chemical fixation: Glutaraldehyde 2.5%

cacodylate buffer 0,1M, pH 6,4 and 6

Muscle strip Optical

Microscopy

HES

Double Contrast Sirius Red

M M

M

Sarcoplasme

L Control

1µm

I band

A band M line Z line

L M Control

100µm

100µm

TECHNAI F20 200KV by FEI Uranyl acetate Lead citrate

grid

Ultrathin sections Fillet (left): Brine Injection

Fillet (right): Dry Salt Control

Smoking

PROCESS

Olympus BX61 + camera DP 71

c a b

Transmission Electron Microscopy n=6

Lipid

Optical Microscopy

Transmission Electron Microscopy

Dry Salt + Smoking

1µm Brine Injection

1µm

Brine Injection + Smoking

1µm

Dry Salt

1µm

Break Sarcomeres Myofibrils Swelling

Dry Salt+Smoking

20,73

11,57 15,40

14,40 16,67

0 5 10 15 20 25 30

Control B I B I+Smoking D S D S+Smoking

Average size of ECS

% Area of Extracellular Spaces/processes a

a

b

ab ab

Salting substantially degrades muscle ultrastructure with in particular a significant solubilization of the Z-lines.

Salting by brine injection leads to swelling of the myofibrils and almost complete

solubilization of the Z lines.

Control

HES = size of the extracellular spaces after brine injection.

Sirius red = no significant effect on the connective tissue (red).

Dry salt salting shows no difference in the extracellular size compared to control

Brine Injection Brine Injection+Smoking Dry Salt

100µm 100µm

1 UR370 Qualité des Produits Animaux (QuaPA), Centre de recherches Auvergne-Rhône-Alpes, F-63122 St-Genès-Champanelle (France)

2 MRI-COMET, Hôpital Saint Eloi, F-34091 Montpellier (France)

Mitochondria Sarcomere

UR370 Qualité des Produits Animaux (QuaPA) Centre de recherches Auvergne-Rhône-Alpes F-63122 St-Genès-Champanelle (France) www.ara.inra.fr

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